Highly validated and characterized monoclonal/polyclonal
antibodies and recombinant
proteins
The majority of AAA Biotech’s antibodies are highly validated and can be use in multiple
applications such as ELISA, FC,
ICC, IF, IHC, IP, WB, etc. We have antibodies available for rare species, in multiple conjugated
forms or recombinant
antibodies.
As for our high quality proteins, the majority have 90% purity, detected by SDS-PAGE while some are
available in
different tags such as Flag, GST, His, MBP, etc. We also carry high quality native and biologically
active proteins.
AAA Biotech is constantly working to expand our capacity to provide recombinant proteins and
antibodies to most
target proteins.
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Rat MPO monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Rat MPO monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄⧉products_description => string (823) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Rat MPO monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
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This assay has high sensitivity and excellent specificity for detection of LN. No significant cross-reactivity or interference between LN and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between LN and all the analogues, therefore, cross reaction may still exist in some cases.
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1365) "Principle of the Assay: LN ELISA kit applies the competitive enzyme immunoas...
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Principle of the Assay: LN ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-LN antibody and an LN-HRP conjugate. The assay sample and buffer are incubated together with LN-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the LN concentration since LN from samples and LN-HRP conjugate compete for the anti-LN antibody binding site. Since the number of sites is limited, as more sites are occupied by LN from the sample, fewer sites are left to bind LN-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The LN concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This LN ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Porcine LN. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
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aaa16759 porcine this assay has high sensitivity and excellent specificity for detection of ln no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa16759_sc elisa kit laminin gamma 2 lamc2 b2t csf ebr2 bm600 ebr2a lamb2t lamnb2 subunit 100kda chain 140 kda nicein kalinin ladsin epiligrin cell scattering factor large adhesive scatter 121,604 da 100 5 lamc2_human 34232 caa78729.1 q13753 q02536 q02537 q13752 q14941 q14df7 q5vye8 gene 226700 cardiovascular samples serum plasma culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 ng ml gamma2 chain140 da100 competitive1.0
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This assay has high sensitivity and excellent specificity for detection of human C-MAPT/C-TAU. No significant cross-reactivity or interference between human C-MAPT/C-TAU and analogues was observed.
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Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
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Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
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Human cleaved microtubule-associated protein tau (C-MAPT/C-TAU) ELISA kit; cleaved form of DDPAC; FLJ31424; FTDP-17; MAPTL; MGC138549; MSTD; MTBT1; MTBT2; PPND; TAU; G protein beta1/gamma2 subunit-interacting factor 1; microtubule-associated protein tau; isoform 4; cleaved microtubule-associated protein tau
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Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for C-MAPT/C-TAU has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any C-MAPT/C-TAU present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for C-MAPT/C-TAU is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of C-MAPT/C-TAU bound in the initial step. The color development is stopped and the intensity of the color is measured.
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aaa18385 human this assay has high sensitivity and excellent specificity for detection of c mapt tau no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18385_td elisa kit cleaved microtubule associated protein form ddpac flj31424 ftdp 17 maptl mgc138549 mstd mtbt1 mtbt2 ppnd g beta1 gamma2 subunit interacting factor 1 isoform 4 samples serum plasma cerebrospinal fluid csf tissue homogenates cell lysates type quantitative sandwich range 62.5 pg ml 4000 < 15.6 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in ftdp17 factor1 isoform4
IHC (Immunohistochemistry)||Immunohistochemical analysis of Laminin alpha 5 staining in human lung cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.||AAA17816_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Laminin alpha 5 expression in JAR (A), A431 (B), RAW264.7 (C) whole cell lysates.<br>(Predicted band size: 399 kD; Observed band size: 400 kD)||AAA17816_WB.jpg
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Immunogen||KLH-conjugated synthetic peptide encompassing a sequence within the center region of human Laminin alpha 5. The exact sequence is proprietary.
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aaa17816 human mouse polyclonal the antibody was purified by immunogen affinity chromatography liquid in 0.42 potassium phosphate 0.87 sodium chloride ph 7.3 30 glycerol and 0.01 azide recognizes endogenous levels of laminin alpha 5 protein western blot wb immunohistochemistry ihc immunoprecipitation ip 1 500 1000 ih 100 200 10 analysis expression jar a a431 b raw264.7 c whole cell lysates aaa17816_wb immunohistochemical staining brain formalin fixed paraffin embedded tissue section pre treated using heat mediated antigen retrieval with citrate buffer 6.0 then incubated at room temperature detected an hrp conjugated compact polymer system dab used as chromogen counterstained haematoxylin mounted dpx aaa17816_ihc anti kiaa0533 kiaa1907 subunit 11 15 lama5 chain lama5_human 21264602 np_005551.3 o15230 nm_005560.4 q8tdf8 q8wza7 q9h1p1 601033 source rabbit entrez gene 3911 16776 swissprot q61001 klh synthetic peptide encompassing sequence within center region exact is proprietary ph7.3 alpha5 ip1 ih100 buffer6.0 subunit11
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Human IGHG2 monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
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aaa22763 human no cross reaction with other factors typical testing data standard curve for reference only aaa22763_sc elisa kit immunoglobulin heavy constant gamma 2 g2m marker ighg2 samples serum plasma or cell culture supernatant and organizations in the natural recombinant igfbp 3 concentration assay type sandwich detection range 10 ng ml 0.156 sensitivity 0.05 intra precision <= 8 inter 12 gamma2 igfbp3 range10 <=8 inter12
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Samples||Rat Serum, Plasma, Body Fluids, Tissue Lysates Or Cell Culture Supernates!!Assay Type||Sandwich!!Detection Range||0 uIU/ml-140 uIU/ml!!Sensitivity||< 5 uIU/ml
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⇄⧉products_description => string (1718) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
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Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti-Insulin monoclonal antibody was pre-coated onto 96-well plates. And the HRP conjugated anti-Insulin polyclonal antibody was used as detection antibodies. The standards, test samples and HRP conjugated detection antibody were added to the wells subsequently, and wash with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the Insulin amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of Insulin can be calculated!!Background/Introduction: Insulin, synthesized by the beta cells of the islets of Langerhans, consists of 2 dissimilar polypeptide chains, A and B, which are linked by 2 disulfide bonds. The human insulin gene contains 3 exons; exon 2 encodes the signal peptide, the B chain, and part of the C peptide, while exon 3 encodes the remainder of the C peptide and the A chain. Insulin has a potent acute antiinflammatory effect, including a reduction in intranuclear NF-kappa-B, an increase in IKB, and decreases in the generation of reactive oxygen species. It causes cells in the liver, muscle, and fat tissue to take up glucose from the blood, storing it as glycogen inside these tissues, and improved insulin-stimulated glucose uptake after endurance training results from hemodynamic adaptations as well as increased cellular protein content of individual insulin signaling components and molecules involved in glucose transport and metabolism.
⇄⧉search_terms => string (434) "aaa13511 human quantitative selisa eia for detection of leptin in serum plas...
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aaa13511 human quantitative selisa eia for detection of leptin in serum plasma body fluids tissue lysates or cell culture supernates typical testing data standard curve reference only aaa13511_sc elisa kit lep ob obs lepd obese protein obesity factor mouse homolog murine 18,641 da lep_human 4557715 np_000221.1 p41159 nm_000230.2 o15158 q56a88 164160 samples rat assay type sandwich range 0 uiu ml 140 sensitivity < 5 range0 ml140 <5
⇄⧉products_description => string (830) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Porcine GM-CSF monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
Amoebiasis Pathway||167324!!Amoebiasis Pathway||167191!!Calcineurin-regulated NFAT-dependent Transcription In Lymphocytes Pathway||137993!!Calcium Signaling In The CD4+ TCR Pathway||137941!!Cytokine Signaling In Immune System Pathway||366171!!Cytokine-cytokine Receptor Interaction Pathway||83051!!Cytokine-cytokine Receptor Interaction Pathway||460!!Cytokines And Inflammatory Response Pathway||198794!!Fc Epsilon RI Signaling Pathway||83082!!Fc Epsilon RI Signaling Pathway||493
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aaa12922 porcine typical testing data standard curve for reference only aaa12922_sc elisa kit granulocyte macrophage colony stimulating factor gm csf 2 csf2 gmcsf molgramostin sargramostim 16,295 da csf2_human 27437030 np_000749.2 p04141 nm_000758.3 q14ce8 q2vpi8 q8nfi6 138960 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision to5
⇄⧉products_description => string (829) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Chicken IL-12 monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄⧉search_terms => string (580) "aaa12539 chicken no cross reaction with other factors typical testing data s...
$value[6]['_source']['search_terms']
aaa12539 chicken no cross reaction with other factors typical testing data standard curve for reference only aaa12539_sc elisa kit interleukin 12 il 12a il12a p35 clmf nfsk nksf1 subunit alpha il35 chain nf cell stimulatory factor 1 nk cytotoxic lymphocyte maturation 35 kda natural killer 24,874 da il12a_human 4323579 aad16432.1 p29459 q96qz1 161560 samples serum plasma or culture supernatant and organizations in the recombinant igm concentration assay type sandwich detection range 1000 ng ml 15.6 sensitivity 5 intra precision interleukin12 factor1 maturation35 sensitivity5
⇄⧉specificity => string (181) "This assay has high sensitivity and excellent specificity for detection of h...
$value[7]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human WARS. No significant cross-reactivity or interference between human WARS and analogues was observed.
⇄purity => string (3) "N/A"
$value[7]['_source']['purity']
⇄form => string (3) "N/A"
$value[7]['_source']['form']
⇄concentration => string (3) "N/A"
$value[7]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[7]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[7]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
Human tryptophanyl-tRNA synthetase; WARS ELISA Kit; GAMMA-2; IFI53; IFP53; interferon-induced protein 53; tryptophan tRNA ligase 1; cytoplasmic; tryptophanyl-tRNA synthetase
⇄products_gene_name => string (4) "WARS"
$value[7]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[7]['_source']['products_gene_name_syn']
⇄⧉products_description => string (731) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[7]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for WARS has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any WARS present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for WARS is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of WARS bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[7]['_source']['products_references']
⇄⧉products_related_diseases => string (211) "Nervous System Diseases||3708!!Cardiovascular Diseases||1603!!Brain Diseases...
$value[7]['_source']['products_related_diseases']
Nervous System Diseases||3708!!Cardiovascular Diseases||1603!!Brain Diseases||1568!!Poisoning||918!!Pain||916!!Heart Diseases||716!!Liver Diseases||363!!Inflammation||349!!Hypertension||316!!Kidney Diseases||261
⇄⧉search_terms => string (667) "aaa15440 human this assay has high sensitivity and excellent specificity for...
$value[7]['_source']['search_terms']
aaa15440 human this assay has high sensitivity and excellent specificity for detection of wars no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15440_td elisa kit tryptophanyl trna synthetase gamma 2 ifi53 ifp53 interferon induced protein 53 tryptophan ligase 1 cytoplasmic isoform a hwrs trprs 53,165 da wrs sywc_human 47419914 np_004175.2 p23381 nm_004184.3 p78535 q502y0 q53xb6 q9udi5 q9udl3 a6ngn1 a6nid3 191050 samples serum plasma tissue homogenates cell lysates type quantitative sandwich range 0.312 ng ml 20 < 0.078 intra precision within an cv gamma2 protein53 ligase1 ml20
⇄products_name => string (38) "S100 Calcium Binding Protein B (S100B)"
$value[8]['_source']['products_name']
⇄products_name_oem => string (54) "Mouse S100 Calcium Binding Protein B (S100B) ELISA Kit"
$value[8]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[8]['_source']['products_name_syn']
⇄products_gene_name => string (5) "S100B"
$value[8]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[8]['_source']['products_gene_name_syn']
⇄⧉products_description => string (676) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
$value[8]['_source']['products_description']
Principle of the Assay: This experiment use double-sandwich elisa technique and the ELISA Kit provided is typical. The pre-coated antibody is Mouse S100B monoclonal antibody and the detecting antibody is polyclonal antibody with biotin labeled. Samples and biotin labeling antibody are added into ELISA plate wells and washed out with PBS or TBS. Then Avidin-peroxidase conjugates are added to ELISA wells in order; Use TMB substrate for coloring after reactant thoroughly washed out by PBS or TBS. TMB turns into blue in peroxidase catalytic and finally turns into yellow under the action of acid. The color depth and the testing factors in samples are positively correlated.
⇄products_references => string (3) "N/A"
$value[8]['_source']['products_references']
⇄⧉products_related_diseases => string (224) "Nervous System Diseases||525!!Brain Diseases||435!!Cardiovascular Diseases||...
Activated TLR4 Signalling Pathway||106400!!Advanced Glycosylation Endproduct Receptor Signaling Pathway||187092!!Cytosolic Sensors Of Pathogen-associated DNA Pathway||576255!!DEx/H-box Helicases Activate Type I IFN And Inflammatory Cytokines Production Pathway||833822!!Immune System Pathway||106386!!Innate Immune System Pathway||106387!!MyD88 Cascade Initiated On Plasma Membrane Pathway||205107!!MyD88 Dependent Cascade Initiated On Endosome Pathway||187081!!MyD88-independent Cascade Pathway||106401!!MyD88:Mal Cascade Initiated On Plasma Membrane Pathway||106390
⇄sp_protein_name => string (14) "Protein S100-B"
$value[8]['_source']['sp_protein_name']
⇄⧉sp_protein_name_syn => string (84) "S-100 protein beta chain; S-100 protein subunit beta; S100 calcium-binding p...
$value[8]['_source']['sp_protein_name_syn']
S-100 protein beta chain; S-100 protein subunit beta; S100 calcium-binding protein B
⇄⧉search_terms => string (408) "aaa12482 mouse no cross reaction with other factors typical standard curve t...
$value[8]['_source']['search_terms']
aaa12482 mouse no cross reaction with other factors typical standard curve testing data aaa12482_td elisa kit s100 calcium binding protein b s100b nef s100beta s 100 subunit beta chain neural 10,713 da s100b_human 12804681 aah01766.1 p04271 d3dsn6 176990 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision to5
⇄⧉products_description => string (825) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[9]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Rat G-CSF monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄products_references => string (3) "N/A"
$value[9]['_source']['products_references']
⇄⧉products_related_diseases => string (226) "Disease Susceptibility||6!!Nervous System Diseases||4!!Neutropenia||3!!Leuko...
$value[9]['_source']['products_related_diseases']
Disease Susceptibility||6!!Nervous System Diseases||4!!Neutropenia||3!!Leukopenia||2!!Anemia||2!!Leukemia, Myeloid, Acute||2!!Breast Neoplasms||1!!Peripheral Nervous System Diseases||1!!Pulmonary Fibrosis||1!!Brain Injuries||1
⇄⧉search_terms => string (452) "aaa12821 rat no cross reaction with other factors typical testing data stand...
$value[9]['_source']['search_terms']
aaa12821 rat no cross reaction with other factors typical testing data standard curve for reference only aaa12821_sc elisa kit granulocyte colony stimulating factor g csf 3 csf3 gcsf csf3os c17orf33 filgrastim lenograstim pluripoietin 18,434 da inn csf3_human 183041 aaa35882.1 p09919 a8mxr7 138970 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision to5
⇄⧉specificity => string (182) "Human CD3D & CD3E Heterodimer.<br>Has cross-reactivity in ELISA and IHC with...
$value[10]['_source']['specificity']
Human CD3D & CD3E Heterodimer.<br>Has cross-reactivity in ELISA and IHC with Human CD3e/CD3 epsilon Protein.<br>No cross-reactivity in ELISA and IHC with Human CD3d/CD3 delta Protein
⇄purity => string (9) "Protein A"
$value[10]['_source']['purity']
⇄form => string (38) "Liquid; 0.2um filtered solution in PBS"
$value[10]['_source']['form']
⇄concentration => string (3) "N/A"
$value[10]['_source']['concentration']
⇄⧉storage_stability => string (261) "This antibody can be stored at 2-8 degree C for one month without detectable...
$value[10]['_source']['storage_stability']
This antibody can be stored at 2-8 degree C for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20 degree C to -80 degree C. Preservative-Free. Avoid repeated freeze-thaw cycles.
IHC (Immunohistchemistry)||Immunochemical staining CD3 in cynomolgus lymph node with rabbit monoclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.||AAA27755_IHC6.png!!IHC (Immunohistochemistry)||Immunochemical staining CD3 in cynomolgus spleen with rabbit monoclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.||AAA27755_IHC5.png!!FCM (Flow Cytometry)||Flow cytometric analysis of Human CD3E expression on human whole blood lymphocytes. Cells were stained with purified anti-Human CD3E, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes.||AAA27755_FCM4.png!!IHC (Immunohistochemistry)||Immunochemical staining of human CD3E in cynomolgus macaque lymphnode with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).||AAA27755_IHC3.png!!IHC (Immunohistochemistry)||Immunochemical staining of human CD3E in cynomolgus macaque tonsil with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).||AAA27755_IHC2.png!!IHC (Immunohistochemistry)||Immunochemical staining CD3E in human tonsil with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).||AAA27755_IHC.png
Adaptive Immune System Pathway||366160!!CXCR4-mediated Signaling Events Pathway||137910!!Chagas Disease (American Trypanosomiasis) Pathway||147809!!Chagas Disease (American Trypanosomiasis) Pathway||147795!!Costimulation By The CD28 Family Pathway||119552!!Downstream TCR Signaling Pathway||106418!!Downstream Signaling In Naive CD8+ T Cells Pathway||138018!!Generation Of Second Messenger Molecules Pathway||106417!!HTLV-I Infection Pathway||373901!!HTLV-I Infection Pathway||373889
⇄⧉products_description => string (828) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[11]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Porcine PDGF monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄⧉search_terms => string (537) "aaa12654 porcine no cross reaction with other factors typical testing data s...
$value[11]['_source']['search_terms']
aaa12654 porcine no cross reaction with other factors typical testing data standard curve for reference only aaa12654_sc elisa kit platelet derived growth factor pdgf beta polypeptide pdgfb sis ssv ibgc5 pdgf2 c 2 subunit b becaplermin chain proto oncogene simian sarcoma viral v homolog 25,502 da inn pdgfb_human 338209 aaa60552.1 p01127 p78431 q15354 q6fhe7 q9uf23 g3xag8 615483 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision c2 to5
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[12]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human F13A1. No significant cross-reactivity or interference between human F13A1 and analogues was observed.
⇄purity => string (3) "N/A"
$value[12]['_source']['purity']
⇄form => string (3) "N/A"
$value[12]['_source']['form']
⇄concentration => string (3) "N/A"
$value[12]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[12]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[12]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
Human Coagulation Factor XIII A1 Polypeptide (F13A1) ELISA kit; RP11-232H4.1; F13A; FSF; A subunit; TGase; bA525O21.1 (coagulation factor XIII; A1 polypeptide) ; coagulation factor XIII A1 subunit; coagulation factor XIII; A polypeptide; factor XIIIa; fibrin stabilizin; coagulation factor XIII; A1 polypeptide
⇄products_gene_name => string (5) "F13A1"
$value[12]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[12]['_source']['products_gene_name_syn']
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[12]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for F13A1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any F13A1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for F13A1 is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of F13A1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[12]['_source']['products_references']
⇄⧉products_related_diseases => string (230) "Cardiovascular Diseases||13!!Factor XIII Deficiency||10!!Heart Diseases||6!!...
⇄⧉ncbi_protein_info => string (346) "coagulation factor XIII A chain; TGase; factor XIIIa; fibrinoligase; FSF, A ...
$value[12]['_source']['ncbi_protein_info']
coagulation factor XIII A chain; TGase; factor XIIIa; fibrinoligase; FSF, A subunit; coagulation factor XIIIa; transglutaminase A chain; transglutaminase. plasma; fibrin stabilizing factor, A subunit; coagulation factor XIII, A polypeptide; protein-glutamine gamma-glutamyltransferase A chain; bA525O21.1 (coagulation factor XIII, A1 polypeptide)
⇄ncbi_chrom_loc => string (3) "N/A"
$value[12]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (4) "2162"
$value[12]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (9) "83,267 Da"
$value[12]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (379) "Common Pathway||106060!!Complement And Coagulation Cascades Pathway||83073!!...
$value[12]['_source']['ncbi_pathways']
Common Pathway||106060!!Complement And Coagulation Cascades Pathway||83073!!Complement And Coagulation Cascades Pathway||484!!Formation Of Fibrin Clot (Clotting Cascade) Pathway||106057!!Hemostasis Pathway||106028!!Platelet Activation, Signaling And Aggregation Pathway||106034!!Platelet Degranulation Pathway||106050!!Response To Elevated Platelet Cytosolic Ca2+ Pathway||106048
⇄sp_protein_name => string (31) "Coagulation factor XIII A chain"
$value[12]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (77) "Protein-glutamine gamma-glutamyltransferase A chain; Transglutaminase A chain"
⇄⧉search_terms => string (665) "aaa15267 human this assay has high sensitivity and excellent specificity for...
$value[12]['_source']['search_terms']
aaa15267 human this assay has high sensitivity and excellent specificity for detection of f13a1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15267_td elisa kit coagulation factor xiii a1 polypeptide rp11 232h4.1 f13a fsf a subunit tgase ba525o21.1 xiiia fibrin stabilizin chain fibrinoligase transglutaminase plasma stabilizing protein glutamine gamma glutamyltransferase 83,267 da f13a_human 119395709 np_000120.2 p00488 nm_000129.3 q59ha7 q8n6x2 q96p24 q9bx29 gene+613225 samples serum type quantitative sandwich range 0.625 ng ml 40 < 0.156 intra precision within an cv ml40
⇄⧉products_description => string (830) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[13]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Chicken GM-CSF monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
Amoebiasis Pathway||167324!!Amoebiasis Pathway||167191!!Calcineurin-regulated NFAT-dependent Transcription In Lymphocytes Pathway||137993!!Calcium Signaling In The CD4+ TCR Pathway||137941!!Cytokine Signaling In Immune System Pathway||366171!!Cytokine-cytokine Receptor Interaction Pathway||83051!!Cytokine-cytokine Receptor Interaction Pathway||460!!Cytokines And Inflammatory Response Pathway||198794!!Fc Epsilon RI Signaling Pathway||83082!!Fc Epsilon RI Signaling Pathway||493
⇄⧉search_terms => string (433) "aaa12941 chicken typical testing data standard curve for reference only aaa1...
$value[13]['_source']['search_terms']
aaa12941 chicken typical testing data standard curve for reference only aaa12941_sc elisa kit granulocyte macrophage colony stimulating factor gm csf 2 csf2 gmcsf molgramostin sargramostim 16,295 da csf2_human 27437030 np_000749.2 p04141 nm_000758.3 q14ce8 q2vpi8 q8nfi6 138960 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 2000 pg ml 31.2 sensitivity up to 12 intra precision to12
⇄⧉products_description => string (827) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[14]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Human GAL-3 monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄⧉search_terms => string (571) "aaa22435 human no cross reaction with other factors typical testing data sta...
$value[14]['_source']['search_terms']
aaa22435 human no cross reaction with other factors typical testing data standard curve for reference only aaa22435_sc elisa kit galectin 3 gal lectin galactoside binding soluble lgals3 l31 gal3 mac2 cbp35 galbp galig lgals2 l 29 35 kda mac 2 antigen ige protein laminin galactose specific carbohydrate 26,152 da cbp 31 leg3_human 2385452 baa22164.1 p17931 q16005 q6iba7 q96j47 b2rc38 153619 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 10 ng ml 0.156 sensitivity up to 0.05 intra precision galectin3 l29 cbp31 range10
⇄⧉specificity => string (193) "This assay has high sensitivity and excellent specificity for detection of m...
$value[15]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of mouse C-MET/HGFR. No significant cross-reactivity or interference between mouse C-MET/HGFR and analogues was observed.
⇄purity => string (3) "N/A"
$value[15]['_source']['purity']
⇄form => string (3) "N/A"
$value[15]['_source']['form']
⇄concentration => string (3) "N/A"
$value[15]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[15]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[15]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
Mouse Hepatocyte Growth Factor Receptor (C-MET/HGFR) ELISA Kit; AUTS9; HGFR; RCCP2; c-Met; HGF receptor; SF receptor; met proto-oncogene; met proto-oncogene tyrosine kinase; oncogene MET; scatter factor receptor; met proto-oncogene (hepatocyte growth factor receptor)
⇄products_gene_name => string (3) "MET"
$value[15]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[15]['_source']['products_gene_name_syn']
⇄⧉products_description => string (755) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[15]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for C-MET/HGFR has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any C-MET/HGFR present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for C-MET/HGFR is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of C-MET/HGFR bound in the initial step. The color development is stopped and the intensity of the color is measured.
HGF/SF receptor; Proto-oncogene c-Met; Scatter factor receptor; SF receptor; Tyrosine-protein kinase Met
⇄sp_gene_name => string (3) "Met"
$value[15]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (25) "HGF receptor; SF receptor"
$value[15]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (9) "MET_MOUSE"
$value[15]['_source']['sp_entry_name']
⇄sp_mim => string (3) "N/A"
$value[15]['_source']['sp_mim']
⇄sp_interactions => string (8) "FLNA||12"
$value[15]['_source']['sp_interactions']
⇄products_url => string (3) "N/A"
$value[15]['_source']['products_url']
⇄products_viewed => string (1) "0"
$value[15]['_source']['products_viewed']
⇄⧉search_terms => string (640) "aaa15709 mouse this assay has high sensitivity and excellent specificity for...
$value[15]['_source']['search_terms']
aaa15709 mouse this assay has high sensitivity and excellent specificity for detection of c met hgfr no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15709_td elisa kit proto oncogene hepatocyte growth factor receptor auts9 rccp2 hgf sf tyrosine kinase scatter par4 ai838057 protein 153,549 da met_mouse 125485 p16056.1 p16056 q62125 samples serum plasma tissue homogenates type quantitative sandwich range 0.078 ng ml 5 <0.02 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in ml5
⇄⧉products_description => string (1104) "Intended Uses: This immunoassay kit allows for the in vitro quantitative det...
$value[16]['_source']['products_description']
Intended Uses: This immunoassay kit allows for the in vitro quantitative determination of target antigen concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.<br><br>Principle of the Assay: The microtiter plate provided in this kit has been pre-coated with an antibody specific to target antigen. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for target antigen and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain target antigen, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of target antigen in the samples is then determined by comparing the O.D. of the samples to the standard curve.
⇄products_references => string (3) "N/A"
$value[16]['_source']['products_references']
⇄⧉products_related_diseases => string (80) "Ovarian Diseases||1!!Nervous System Diseases||1!!Nervous System Malformation...
Agrin-like protein; EGF-like, fibronectin type-III and laminin G-like domain-containing protein
⇄sp_gene_name => string (6) "EGFLAM"
$value[16]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (13) "AGRINL; AGRNL"
$value[16]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (11) "EGFLA_HUMAN"
$value[16]['_source']['sp_entry_name']
⇄sp_mim => string (3) "N/A"
$value[16]['_source']['sp_mim']
⇄sp_interactions => string (3) "N/A"
$value[16]['_source']['sp_interactions']
⇄products_url => string (3) "N/A"
$value[16]['_source']['products_url']
⇄products_viewed => string (1) "0"
$value[16]['_source']['products_viewed']
⇄⧉search_terms => string (472) "aaa23290 human typical testing data standard curve for reference only aaa232...
$value[16]['_source']['search_terms']
aaa23290 human typical testing data standard curve for reference only aaa23290_sc elisa kit pikachurin agrin like protein egf fibronectin type iii and laminin g domain containing egflam agrinl agrnl isoform 5 domains pika 16,588 da egfla_human 328927010 np_001192230.1 q63hq2 nm_001205301.1 q5u643 q6p3v1 q8n124 q8n197 q8n7y0 q8n8n5 q8nal2 a8k6d7 assay sandwich detection range 0.312 20 ng ml sensitivity 0.19ng intra cv <=3.4 inter <=7.9 recovery 102 isoform5 recovery102
⇄⧉specificity => string (171) "This assay has high sensitivity and excellent specificity for detection of I...
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This assay has high sensitivity and excellent specificity for detection of IL-12. No significant cross-reactivity or interference between IL-12 and analogues was observed.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
$value[17]['_source']['form']
⇄concentration => string (3) "N/A"
$value[17]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[17]['_source']['storage_stability']
Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
⇄⧉etc_term1 => string (152) "Assay Type||Sandwich!!Samples||Serum, plasma, tissue homogenates and other b...
$value[17]['_source']['etc_term1']
Assay Type||Sandwich!!Samples||Serum, plasma, tissue homogenates and other biological fluids!!Detection Range||15.625-1000pg/ml!!Sensitivity||9.375pg/ml
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[17]['_source']['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄⧉search_terms => string (596) "aaa27583 hamster this assay has high sensitivity and excellent specificity f...
$value[17]['_source']['search_terms']
aaa27583 hamster this assay has high sensitivity and excellent specificity for detection of il 12 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa27583_sc elisa kit interleukin 12a il12a p35 clmf nfsk nksf1 subunit alpha 24,874 da cytotoxic lymphocyte maturation factor 35 kda nk cell stimulatory chain 1 4323579 aad16432.1 p29459 q96qz1 m65291 mrna samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 15.625 1000pg ml 9.375pg intra precision cv il12 factor35 chain1
⇄⧉testing_protocols => string (1615) "IF (Immunofluorescence)||Immunofluorescence analysis of HeLa cells using SFP...
$value[18]['_source']['testing_protocols']
IF (Immunofluorescence)||Immunofluorescence analysis of HeLa cells using SFPQ antibody at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.||AAA10716_IF9.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded mouse heart using SFPQ antibody at dilution of 1:100 (40x lens).||AAA10716_IHC8.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded mouse brain using SFPQ antibody at dilution of 1:100 (40x lens).||AAA10716_IHC7.jpg!!IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded mouse lung using SFPQ antibody at dilution of 1:100 (40x lens).||AAA10716_IHC6.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human stomach using SFPQ antibody at dilution of 1:100 (40x lens).||AAA10716_IHC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human esophageal cancer using SFPQ antibody at dilution of 1:100 (40x lens).||AAA10716_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human lung cancer using SFPQ antibody at dilution of 1:100 (40x lens).||AAA10716_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat brain using SFPQ antibody at dilution of 1:100 (40x lens).||AAA10716_IHC2.jpg!!WB (Western Blot)||Western blot analysis of extracts of various cell lines, using SFPQ antibody at 1:1000 dilution.<br>Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.<br>Lysates/proteins: 25ug per lane.<br>Blocking buffer: 3% nonfat dry milk in TBST.<br>Detection: ECL Basic Kit.<br>Exposure time: 1s.||AAA10716_WB.jpg
⇄etc_term1 => string (3) "N/A"
$value[18]['_source']['etc_term1']
⇄⧉etc_term2 => string (122) "Immunogen||Recombinant fusion protein containing a sequencecorresponding to ...
$value[18]['_source']['etc_term2']
Immunogen||Recombinant fusion protein containing a sequencecorresponding to amino acids 578-707 of human SFPQ(NP_005057.1)
⇄⧉specificity => string (171) "This assay has high sensitivity and excellent specificity for detection of I...
$value[19]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of IL-12. No significant cross-reactivity or interference between IL-12 and analogues was observed.
⇄purity => string (3) "N/A"
$value[19]['_source']['purity']
⇄form => string (3) "N/A"
$value[19]['_source']['form']
⇄concentration => string (3) "N/A"
$value[19]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[19]['_source']['storage_stability']
Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[19]['_source']['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄⧉search_terms => string (605) "aaa17599 human this assay has high sensitivity and excellent specificity for...
$value[19]['_source']['search_terms']
aaa17599 human this assay has high sensitivity and excellent specificity for detection of il 12 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17599_sc elisa kit interleukin p70 clmf p35 cytotoxic lymphocyte maturation factor 35 kda subunit 12a il12a nfsk nksf1 alpha 24,874 da nk cell stimulatory chain 1 il12a_human 4323579 aad16432.1 p29459 q96qz1 161560 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 15.625 1000pg ml 9.375pg intra precision cv il12 factor35 chain1
