Search results for "small-hydrophobic-protein"

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Structural Formula

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by DTT oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Dehydroepiandrosterone (DHEA), Polyclonal Antibody (Cat# AAA2006064)

Full Name

Polyclonal Antibody to Dehydroepiandrosterone (DHEA)

Reactivity

General

Applications

ICC, IHC, EIA, WB

Purity

Affinity Chromatography

Pricing

$180/0.1 mL | $220/0.2 mL | $390/0.5 mL | $475/1 mL | $1,320/5x1 mL

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Immunohistochemistry (IHC) (Staining MMP12 in human lung tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 3% BSA for 0. 5 hour at room temperature; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody (1/25) for 1 hours at 37°C. A undiluted biotinylated goat polyvalent antibody was used as the secondary antibody.)

MMP12, Polyclonal Antibody (Cat# AAA9207292)

Full Name

MMP12 Antibody (C-term)

Gene Names

MMP12; ME; HME; MME; MMP-12

Reactivity

Human, mouse

Applications

WB, EIA, IHC-P, IF

Purity

Purified Rabbit Polyclonal Antibody (Pab)

Pricing

$415/0.4 mL | $185/0.08 mL | $1,625/5x0.4 mL

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Testing Data (TD) (Figure 1. SDS-PAGE analysis (12.%) of 3 ul of recombinant ChimChagas 2. Purity is > 98% as determined by gel electrophoresis.Bands which are slightly smaller correspond to this same protein as it is showed in a western blot performed with a his-tag monoclonal antibody)

ChimChagas2, Recombinant Protein (Cat# AAA505072)

Full Name

Recombinant chimeric antigen ChimChagas2 for Trypanosoma cruzi

Purity

>98% in a SDS-PAGE

Pricing

$900/1 mg | $3,755/5 mg

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Immunohistochemistry (IHC) (Formalin-fixed, paraffin-embedded human Liver tissue stained with FABP5 Mouse Monoclonal Antibody (FABP5/3750).)

FABP5, Monoclonal Antibody (Cat# AAA4380894)

Full Name

FABP5 (Marker of Metastatic Potential in Colorectal Cancer)

Gene Names

FABP5; EFABP; KFABP; E-FABP; PAFABP; PA-FABP

Reactivity

Human

Applications

IHC

Purity

Purified Ab with BSA and Azide at 200ug/ml OR Purified Ab WITHOUT BSA and Azide at 1.0mg/ml

Pricing

$390/0.1 mg (With BSA & Azide at 0.2mg/mL) | $390/0.1 mg (Without BSA & Azide at 1mg/mL) | $215/0.02 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (Without BSA & Azide at 1mg/mL)

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Immunohistochemistry (IHC) (Formalin-fixed, paraffin-embedded human Esophagusstained with FABP5 Mouse Monoclonal Antibody (CPTC-FABP5-3).)

FABP5, Monoclonal Antibody (Cat# AAA4380553)

Full Name

FABP5 (Marker of Metastatic Potential in Colorectal Cancer)

Gene Names

FABP5; EFABP; KFABP; E-FABP; PAFABP; PA-FABP

Reactivity

Human. Others not tested.

Applications

WB, Formalin-Fixed

Purity

Purified Ab with BSA and Azide at 200ug/ml OR Purified Ab WITHOUT BSA and Azide at 1.0mg/ml

Pricing

$390/0.1 mg (With BSA & Azide at 0.2mg/mL) | $390/0.1 mg (Without BSA & Azide at 1mg/mL) | $215/0.02 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (Without BSA & Azide at 1mg/mL)

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Immunohistochemistry (IHC)-Formallin (Formalin-fixed, paraffin-embedded human liver stained with Apolipoprotein D Mouse Monoclonal Antibody (APOD/3414).)

Apolipoprotein D/APOD, Monoclonal Antibody (Cat# AAA4381675)

Full Name

Apolipoprotein D/APOD

Reactivity

Human

Applications

IHC

Purity

Purified Ab with BSA and Azide at 200ug/ml or Purified Ab with BSA and Azide at 200ug/ml or Purified Ab WITHOUT BSA and Azide at 1.0mg/ml

Pricing

$390/0.1 mg (With BSA & Azide at 0.2mg/mL) | $390/0.1 mg (Without BSA & Azide at 1mg/mL) | $215/0.02 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (Without BSA & Azide at 1mg/mL)

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Immunohistochemistry (IHC)-Formallin (Formalin-fixed, paraffin-embedded human liver stained with Apolipoprotein D Mouse Monoclonal Antibody (APOD/3412).)

Apolipoprotein D/APOD, Monoclonal Antibody (Cat# AAA4381674)

Full Name

Apolipoprotein D/APOD

Reactivity

Human

Applications

IHC

Purity

Purified Ab with BSA and Azide at 200ug/ml or Purified Ab with BSA and Azide at 200ug/ml or Purified Ab WITHOUT BSA and Azide at 1.0mg/ml

Pricing

$390/0.1 mg (With BSA & Azide at 0.2mg/mL) | $390/0.1 mg (Without BSA & Azide at 1mg/mL) | $215/0.02 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (With BSA & Azide at 0.2mg/mL) | $1,710/5x0.1 mg (Without BSA & Azide at 1mg/mL)

RESPIRATORY SYNCYTIAL VIRUS MAJOR SURFACE GLYCOPROTEIN G, Monoclonal Antibody (Cat# AAA211900)

Full Name

MOUSE ANTI RESPIRATORY SYNCYTIAL VIRUS MAJOR SURFACE GLYCOPROTEIN G

Reactivity

Viral

Applications

EIA, WB

Pricing

$490/0.2 mg | $2,050/5x0.2 mg

HBcAg, Monoclonal Antibody (Cat# AAA531015)

Full Name

HBcAg antibody

Reactivity

HBV

Applications

User optimized

Pricing

$895/1 mg | $4,010/5x1 mg

HBeAg, Monoclonal Antibody (Cat# AAA531426)

Full Name

HBeAg antibody

Reactivity

HBV

Applications

User optimized

Pricing

$520/1 mg | $2,330/5x1 mg

HBeAg, Recombinant Protein (Cat# AAA537659)

Full Name

HBeAg protein

Applications

User optimized

Purity

> 90% pure

Pricing

$1,710/1 mg | $7,695/5x1 mg

HBcAg, Monoclonal Antibody (Cat# AAA530016)

Full Name

HBcAg antibody

Reactivity

HBV

Applications

User optimized

Hepatitis B Virus PreS2, Polyclonal Antibody (Cat# AAA534255)

Full Name

Hepatitis B Virus PreS2 antibody

Reactivity

Reacts with residues 132-145 of the 42kDa preS2 HBV protein. This sequence represents a B cell epitope.

Applications

WB

Purity

Hepatitis B Virus PreS2 antibody was purified by affinity chromatography.

Pricing

$465/0.1 mg | $2,090/5x0.1 mg

MRP1, Monoclonal Antibody (Cat# AAA531429)

Full Name

MRP1 antibody

Gene Names

Abcc1; Mrp; Mrp1; Abcc1a; Avcc1a

Applications

IHC, FC/FACS

Purity

Culture supernatant

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Western Blot (Sample: Recombinant Osteonectin, Human)

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by Dn oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Osteonectin (ON), Polyclonal Antibody (Cat# AAA2005086)

Full Name

Biotin-Linked Antibody to Osteonectin (ON)

Gene Names

SPARC; ON

Reactivity

Human

Applications

ICC, IHC, IHC-f, IHC-P, IF, WB

Purity

Affinity Chromatography

Pricing

$165/0.1 mL | $205/0.2 mL | $340/0.5 mL | $420/1 mL | $1,210/5x1 mL

alpha 1 Microglobulin, Monoclonal Antibody (Cat# AAA834963)

Full Name

alpha 1 Microglobulin mAb

Gene Names

AMBP; A1M; HCP; ITI; UTI; EDC1; HI30; ITIL; IATIL; ITILC

Applications

EIA, WB

Purity

alpha 1 Microglobulin antibody was purified by ammonium sulfate precipitation

Pricing

$455/0.1 mL | $2,030/5x0.1 mL

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Structural Formula

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by Dn oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Androstenedione (ASD), Polyclonal Antibody (Cat# AAA2014872)

Full Name

Biotin-Linked Antibody to Androstenedione (ASD)

Reactivity

General

Applications

IHC/ IHC-P/ IHC-F, EIA, WB, ICC

Purity

Affinity Chromatography.

Pricing

$190/0.1 mL | $240/0.2 mL | $425/0.5 mL | $515/1 mL | $1,430/5x1 mL

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SDS-PAGE

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by DTT oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Deoxycholate (DC), Polyclonal Antibody (Cat# AAA2001803)

Full Name

Polyclonal Antibody to Deoxycholate (DC)

Reactivity

General

Applications

ICC, IHC, EIA, WB

Purity

Affinity Chromatography

Pricing

$180/0.1 mL | $220/0.2 mL | $390/0.5 mL | $475/1 mL | $1,320/5x1 mL

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Western Blot

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by DTT oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Kallikrein 6 (KLK6), Polyclonal Antibody (Cat# AAA2004619)

Full Name

Biotin-Linked Antibody to Kallikrein 6 (KLK6)

Reactivity

Mouse

Applications

IHC, EIA, WB, ICC

Purity

Affinity Chromatography

Pricing

$165/0.1 mL | $210/0.2 mL | $350/0.5 mL | $430/1 mL | $1,235/5x1 mL

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Western Blot

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by DTT oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Thrombospondin 1 (THBS1), Polyclonal Antibody (Cat# AAA2003532)

Full Name

Biotin-Linked Antibody to Thrombospondin 1 (THBS1)

Gene Names

THBS1; TSP; THBS; TSP1; TSP-1; THBS-1

Reactivity

Human

Applications

IHC, EIA, WB, ICC

Purity

Affinity Chromatography

Pricing

$165/0.1 mL | $205/0.2 mL | $345/0.5 mL | $420/1 mL | $1,215/5x1 mL

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Western Blote

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by DTT oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Arginase (ARG), Monoclonal Antibody (Cat# AAA2007423)

Full Name

Biotin-Linked Antibody to Arginase (ARG)

Reactivity

Human

Applications

IHC, EIA, WB

Purity

Affinity Chromatography

Pricing

$175/0.1 mL | $220/0.2 mL | $380/0.5 mL | $465/1 mL | $1,300/5x1 mL

GLUT1, Polyclonal Antibody (Cat# AAA534829)

Full Name

GLUT1 antibody

Reactivity

Human

Applications

IP, WB

Purity

GLUT1 antibody was purified by affinity chromatography.

Pricing

$920/0.1 mg | $4,130/5x0.1 mg

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Western Blot

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by DTT oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Growth Differentiation Factor 11 (GDF11), Polyclonal Antibody (Cat# AAA2014017)

Full Name

Biotin-Linked Antibody to Growth Differentiation Factor 11 (GDF11)

Gene Names

GDF11; BMP11; BMP-11

Reactivity

Human

Applications

IHC, EIA, WB, ICC

Pricing

$175/0.1 mL | $220/0.2 mL | $375/0.5 mL | $460/1 mL | $1,295/5x1 mL

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Structural Formula

SDS-PAGE ([ DESCRIPTION] Effective Size Range: 10kDa to 70kDa. Protein bands: 10 kDa, 14 kDa, 18 kDa, 22 kDa, 26 kDa, 33 kDa, 44 kDa and 70 kDa. Double intensity bands: The 26 kDa, 18 kDa, 10 kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy. Ready-to-use: No need to heat, dilute or add reducing agents before use. [ STORAGE BUFFER] 62.5mM Tris-H3P04 (pH 7.5 at 25°C), 1 mM EDTA, 2% (w/v) SDS, 100mM DTT, 1 mM NaN3, 0.01 % (w/v) bromo-phenol blue and 33% (v/v) glycerol. [APPLICATION] Accurate protein sizing on SDS-polyacrylamide gels and Western blots. [USAGE] 1. Allow the Marker to reach room temperature and thoroughly mix before use. This will ensure that any solids that may have precipitated at -20°C have returned to solution. Do not boil! 2. Load the following volumes of the Marker on a SDS-polyacrylamide gel. [ LOADING VOLUMES] 3~5uL per well for mini gel; 7uL per well for large gel. Use the same volumes for Western blotting applications. The loading volumes listed above are recommended for gels with a thickness of 0.75~1.0mm. The loading volume should be double for 1.5mm thick gels. [ QUALITY CONTROL] The protein marker, with molecular weight shifts of < or = 5% and minimal band broadening, are confirmed by migration in SDS-PAGE system. Electrophoresis of the Marker on a 13~18% Tris-glycine SDS-polyacrylamide gel resolves 8 individual bands. [IMPORTANT NOTES] 1. The protein marker is conveniently packaged and ready to use. There is no need to heat, dilute or add reducing agents. Do not boil, which may cause band degradation. 2. The molecular weights of the proteins have a lot-to-Iot variation of ~5%. 3. These protein markers are for SDS-PAGE and should not to be used for native electrophoresis or a native gel. These markers are denatured and have SDS in the storage buffer. 4. Don't load too much protein. See recommended load volumes in the manual. 5. Check % gel that is being used if the lands miss. Depending on gel type and/or percentage, you may not see all of the bands. For example, one would not see the smallest bands of the standard on a very low % gel. A high % gel may not resolve the higher MW bands. Homogeneous low percentage gels are recommended for analysis of large proteins and high percentage gels for analysis of small proteins. In high percentage gels (13~18%) large proteins (22~70kDa) can separate, while in low percentage gels (4~8%) small proteins (14 and 10kDa) will migrate with the tracking dye. Longer transfer times or higher transfer voltages may be required for Western blotting of large (>100kDa) proteins. 6. If additional bands are observed in the gel image of the protein ladder, this might be caused by DTT oxidation in the storage buffer. 7. If proteins show a poor transfer, increase voltage, current or length of time for transfer, and pay attention to the SDS from the transfer buffer. SDS will cause the proteins to bind less efficiently to membranes because it disrupts the hydrophobic interaction between the membrane and the protein. If SDS is present in transfer buffer, make sure that there is no more than 0.02% in buffer. 8. Alcohol enhances hydrophobic binding to membrane. Not enough alcohol may prevent binding. [ SHELF LIFE] Storage: -20 degree C, 1 year at -20 degree C. If the product has been stored as directed for one year, its shelf life maybe extended by adding dithiothreitol (Dn) to approximately 50mM.)

Vitamin D3 (VD3), Polyclonal Antibody (Cat# AAA2001576)

Full Name

Biotin-Linked Antibody to Vitamin D3 (VD3)

Reactivity

General

Applications

IHC, EIA, WB, ICC

Purity

Affinity Chromatography

Pricing

$190/0.1 mL | $240/0.2 mL | $425/0.5 mL | $515/1 mL | $1,430/5x1 mL

TACR2, Polyclonal Antibody (Cat# AAA535534)

Full Name

TACR2 antibody

Gene Names

TACR2; SKR; NK2R; NKNAR; TAC2R

Reactivity

Human

Applications

IHC

Purity

TACR2 antibody was purified by affinity chromatography.

Pricing

$885/0.05 mg | $3,965/5x0.05 mg

SLC7A5, Polyclonal Antibody (Cat# AAA535482)

Full Name

SLC7A5 antibody

Gene Names

slc7a5-a; e16; cd98; lat1; 4f2lc; LAT-1; mpe16; slc7a5; slc7a5a

Reactivity

Human

Applications

IHC

Purity

SLC7A5 antibody was purified by affinity chromatography.

Pricing

$885/0.05 mg | $3,965/5x0.05 mg

SLC7A11, Polyclonal Antibody (Cat# AAA535500)

Full Name

SLC7A11 antibody

Gene Names

SLC7A11; xCT; CCBR1

Reactivity

Human

Applications

IHC

Purity

SLC7A11 antibody was purified by affinity chromatography.

Pricing

$885/0.05 mg | $3,965/5x0.05 mg

CD9, Monoclonal Antibody (Cat# AAA532714)

Full Name

CD9 antibody (PE)

Gene Names

CD9; MIC3; MRP-1; BTCC-1; DRAP-27; TSPAN29; TSPAN-29

Reactivity

Human

Applications

FC/FACS, IHC

Pricing

$485/100 Tests | $2,180/5x100 Tests

FABP7, Monoclonal Antibody (Cat# AAA533059)

Full Name

FABP7 antibody

Applications

User optimized

CD9, Monoclonal Antibody (Cat# AAA532713)

Full Name

CD9 antibody (FITC)

Gene Names

CD9; MIC3; MRP-1; BTCC-1; DRAP-27; TSPAN29; TSPAN-29

Reactivity

Human

Applications

FC/FACS, IHC

Pricing

$520/100 Tests | $2,330/5x100 Tests

SLC5A10, Polyclonal Antibody (Cat# AAA535577)

Full Name

SLC5A10 antibody

Gene Names

SLC5A10; SGLT5; SGLT-5

Reactivity

Human

Applications

IHC

Purity

SLC5A10 antibody was purified by affinity chromatography.

Pricing

$885/0.05 mg | $3,965/5x0.05 mg

HBcAg, Monoclonal Antibody (Cat# AAA838788)

Full Name

HBcAg antibody

Applications

EIA

Purity

> 95% pure

Pricing

$225/1 mg | $1,010/5x1 mg

HBsAg, Monoclonal Antibody (Cat# AAA531485)

Full Name

HBsAg antibody

Reactivity

HBV

Applications

User optimized

Pricing

$270/1 mg | $1,210/5x1 mg

FABP7, Monoclonal Antibody (Cat# AAA830972)

Full Name

FABP7 antibody

Applications

User optimized

HBsAg, Monoclonal Antibody (Cat# AAA530171)

Full Name

HBsAg antibody

Reactivity

HBV

Applications

User optimized

Pricing

$270/1 mg | $1,210/5x1 mg

FABP7, Monoclonal Antibody (Cat# AAA533934)

Full Name

FABP7 antibody

Applications

WB

FABP, Monoclonal Antibody (Cat# AAA838773)

Full Name

FABP antibody

Gene Names

FABP4; FABP; AFABP; A-FABP

Applications

EIA, WB

Pricing

$435/1 mg | $1,945/5x1 mg

ILBP, Polyclonal Antibody (Cat# AAA837501)

Full Name

ILBP antibody

Applications

WB

Purity

ILBP antibody was purified by antigen-affinity chromatography

Pricing

$700/0.1 mL | $3,130/5x0.1 mL

SLC7A5, Polyclonal Antibody (Cat# AAA535510)

Full Name

SLC7A5 antibody

Gene Names

slc7a5-a; e16; cd98; lat1; 4f2lc; LAT-1; mpe16; slc7a5; slc7a5a

Reactivity

Human

Applications

IHC

Purity

SLC7A5 antibody was purified by affinity chromatography.

Pricing

$885/0.05 mg | $3,965/5x0.05 mg

TACR2, Polyclonal Antibody (Cat# AAA535544)

Full Name

TACR2 antibody

Gene Names

TACR2; SKR; NK2R; NKNAR; TAC2R

Reactivity

Human

Applications

IHC

Purity

TACR2 antibody was purified by affinity chromatography.

Pricing

$885/0.05 mg | $3,965/5x0.05 mg

RESPIRATORY SYNCYTIAL VIRUS FUSION PROTEIN, Monoclonal Antibody (Cat# AAA212943)

Full Name

MOUSE ANTI RESPIRATORY SYNCYTIAL VIRUS FUSION PROTEIN

Applications

EIA, IF

Pricing

$345/0.1 mg | $1,405/5x0.1 mg

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L-FABP, Monoclonal Antibody (Cat# AAA475267)

Full Name

Anti-L-FABP Mouse mAb

Gene Names

FABP1; FABPL; L-FABP

Reactivity

Human

Applications

EIA

Purity

Affinity purified

Pricing

$440/0.1 mL | $1,530/5x0.1 mL

SCGB1A1, Polyclonal Antibody (Cat# AAA1491014)

Full Name

Rabbit Anti Human SCGB1A1 PolyClonal Antibody

Gene Names

SCGB1A1; UGB; UP1; CC10; CC16; CCSP; UP-1; CCPBP

Reactivity

Human, Mouse, Rat

Applications

WB, IHC

Purity

Affinity Purification

Pricing

$325/0.1 mL | $1,465/5x0.1 mL

< >

L-FABP, Monoclonal Antibody (Cat# AAA475289)

Full Name

Anti-L-FABP Mouse mAb

Gene Names

FABP1; FABPL; L-FABP

Reactivity

Human

Applications

EIA

Purity

Affinity purified

Pricing

$440/0.1 mL | $1,530/5x0.1 mL

Small hydrophobic protein (SH), Recombinant Protein (Cat# AAA1150720)

Full Name

Recombinant Bovine respiratory syncytial virus Small hydrophobic protein (SH)

Purity

Greater or equal to 85% purity as determined by SDS-PAGE.

HBcAg, Monoclonal Antibody (Cat# AAA838247)

Full Name

HBcAg antibody

Applications

EIA

Purity

> 95% pure

Pricing

$225/1 mg | $1,010/5x1 mg

Small hydrophobic protein (SH), Recombinant Protein (Cat# AAA1259395)

Full Name

Recombinant Turkey rhinotracheitis virus Small hydrophobic protein (SH)

Purity

Greater or equal to 85% purity as determined by SDS-PAGE.

Succinate dehydrogenase hydrophobic membrane anchor subunit (sdhD), Recombinant Protein (Cat# AAA1238242)

Full Name

Recombinant Succinate dehydrogenase hydrophobic membrane anchor subunit (sdhD)

Purity

Greater or equal to 85% purity as determined by SDS-PAGE.

Succinate dehydrogenase hydrophobic membrane anchor subunit (sdhD), Recombinant Protein (Cat# AAA1098485)

Full Name

Recombinant Succinate dehydrogenase hydrophobic membrane anchor subunit (sdhD)

Purity

Greater or equal to 85% purity as determined by SDS-PAGE.

Small hydrophobic protein (SH), Recombinant Protein (Cat# AAA1209568)

Full Name

Recombinant Mumps virus Small hydrophobic protein (SH), partial

Purity

Greater or equal to 85% purity as determined by SDS-PAGE.

Pricing

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Reactivity

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109 results for "small-hydrophobic-protein" - showing 1-50

Dehydroepiandrosterone (DHEA), Polyclonal Antibody (Cat# AAA2006064)

MMP12, Polyclonal Antibody (Cat# AAA9207292)

ChimChagas2, Recombinant Protein (Cat# AAA505072)

FABP5, Monoclonal Antibody (Cat# AAA4380894)

FABP5, Monoclonal Antibody (Cat# AAA4380553)

Apolipoprotein D/APOD, Monoclonal Antibody (Cat# AAA4381675)

Apolipoprotein D/APOD, Monoclonal Antibody (Cat# AAA4381674)

RESPIRATORY SYNCYTIAL VIRUS MAJOR SURFACE GLYCOPROTEIN G, Monoclonal Antibody (Cat# AAA211900)

HBcAg, Monoclonal Antibody (Cat# AAA531015)

HBeAg, Monoclonal Antibody (Cat# AAA531426)

HBeAg, Recombinant Protein (Cat# AAA537659)

HBcAg, Monoclonal Antibody (Cat# AAA530016)

Hepatitis B Virus PreS2, Polyclonal Antibody (Cat# AAA534255)

MRP1, Monoclonal Antibody (Cat# AAA531429)

Osteonectin (ON), Polyclonal Antibody (Cat# AAA2005086)

alpha 1 Microglobulin, Monoclonal Antibody (Cat# AAA834963)

Androstenedione (ASD), Polyclonal Antibody (Cat# AAA2014872)

Deoxycholate (DC), Polyclonal Antibody (Cat# AAA2001803)

Kallikrein 6 (KLK6), Polyclonal Antibody (Cat# AAA2004619)

Thrombospondin 1 (THBS1), Polyclonal Antibody (Cat# AAA2003532)

Arginase (ARG), Monoclonal Antibody (Cat# AAA2007423)

GLUT1, Polyclonal Antibody (Cat# AAA534829)

Growth Differentiation Factor 11 (GDF11), Polyclonal Antibody (Cat# AAA2014017)

Vitamin D3 (VD3), Polyclonal Antibody (Cat# AAA2001576)

TACR2, Polyclonal Antibody (Cat# AAA535534)

SLC7A5, Polyclonal Antibody (Cat# AAA535482)

SLC7A11, Polyclonal Antibody (Cat# AAA535500)

CD9, Monoclonal Antibody (Cat# AAA532714)

FABP7, Monoclonal Antibody (Cat# AAA533059)

CD9, Monoclonal Antibody (Cat# AAA532713)

SLC5A10, Polyclonal Antibody (Cat# AAA535577)

HBcAg, Monoclonal Antibody (Cat# AAA838788)

HBsAg, Monoclonal Antibody (Cat# AAA531485)

FABP7, Monoclonal Antibody (Cat# AAA830972)

HBsAg, Monoclonal Antibody (Cat# AAA530171)

FABP7, Monoclonal Antibody (Cat# AAA533934)

FABP, Monoclonal Antibody (Cat# AAA838773)

ILBP, Polyclonal Antibody (Cat# AAA837501)

SLC7A5, Polyclonal Antibody (Cat# AAA535510)

TACR2, Polyclonal Antibody (Cat# AAA535544)

RESPIRATORY SYNCYTIAL VIRUS FUSION PROTEIN, Monoclonal Antibody (Cat# AAA212943)

L-FABP, Monoclonal Antibody (Cat# AAA475267)

SCGB1A1, Polyclonal Antibody (Cat# AAA1491014)

L-FABP, Monoclonal Antibody (Cat# AAA475289)

Small hydrophobic protein (SH), Recombinant Protein (Cat# AAA1150720)

HBcAg, Monoclonal Antibody (Cat# AAA838247)

Small hydrophobic protein (SH), Recombinant Protein (Cat# AAA1259395)

Succinate dehydrogenase hydrophobic membrane anchor subunit (sdhD), Recombinant Protein (Cat# AAA1238242)

Succinate dehydrogenase hydrophobic membrane anchor subunit (sdhD), Recombinant Protein (Cat# AAA1098485)

Small hydrophobic protein (SH), Recombinant Protein (Cat# AAA1209568)

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