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Typical Testing Data/Standard Curve (for reference only)

Human HLA class II histocompatibility antigen, DR beta 5 chain ELISA Kit | HLA-DRB5 elisa kit

Human HLA class II histocompatibility antigen, DR beta 5 chain ELISA Kit

Gene Names
HLA-DRB5; HLA-DRB
Reactivity
Human
Synonyms
HLA class II histocompatibility antigen; DR beta 5 chain; Human HLA class II histocompatibility antigen; DR beta 5 chain ELISA Kit; DR beta-5; DR2-beta-2; Dw2; MHC class II antigen DRB5; HLA-DRB5; HLA-DRB5 elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Specificity
This assay recognizes recombinant and natural Human DRB5. No significant cross-reactivity or interference was observed.
Sequence Length
266
Assay Type
Competitive
Detection Range
1.56-100 ng/mL
Sensitivity
0.16ng/ml
Intra-Assay CV
<=6.3%
Inter-Assay CV
<=9.4%
Recovery
101%
Preparation and Storage
For long term storage, please store the entire kit at -20 degree C.

Typical Testing Data/Standard Curve (for reference only)

Typical Testing Data/Standard Curve (for reference only)
Related Product Information for HLA-DRB5 elisa kit
Intended Uses: This immunoassay kit allows for the in vitro quantitative determination of human hla class ii histocompatibility antigen, dr beta 5 chain,DRB5 concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.

Principle of the Assay||The ELISA is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to DRB5, During the reaction, DRB5 in the sample or standard competes with a fixed amount of biotin-labeled DRB5 for sites on a pre-coated Monoclonal antibody specific to DRB5. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. 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 DRB5 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
Molecular Weight
30,056 Da
NCBI Official Full Name
major histocompatibility complex, class II, DR beta 5
NCBI Official Synonym Full Names
major histocompatibility complex, class II, DR beta 5
NCBI Official Symbol
HLA-DRB5
NCBI Official Synonym Symbols
HLA-DRB
NCBI Protein Information
major histocompatibility complex, class II, DR beta 5
UniProt Protein Name
HLA class II histocompatibility antigen, DR beta 5 chain
UniProt Gene Name
HLA-DRB5
UniProt Entry Name
DRB5_HUMAN

NCBI Description

HLA-DRB5 belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. DRB1 is expressed at a level five times higher than its paralogues DRB3, DRB4 and DRB5. The presence of DRB5 is linked with allelic variants of DRB1, otherwise it is omitted. There are 4 related pseudogenes: DRB2, DRB6, DRB7, DRB8 and DRB9. [provided by RefSeq, Jul 2008]

Uniprot Description

Binds peptides derived from antigens that access the endocytic route of antigen presenting cells (APC) and presents them on the cell surface for recognition by the CD4 T-cells. The peptide binding cleft accommodates peptides of 10-30 residues. The peptides presented by MHC class II molecules are generated mostly by degradation of proteins that access the endocytic route, where they are processed by lysosomal proteases and other hydrolases. Exogenous antigens that have been endocytosed by the APC are thus readily available for presentation via MHC II molecules, and for this reason this antigen presentation pathway is usually referred to as exogenous. As membrane proteins on their way to degradation in lysosomes as part of their normal turn-over are also contained in the endosomal/lysosomal compartments, exogenous antigens must compete with those derived from endogenous components. Autophagy is also a source of endogenous peptides, autophagosomes constitutively fuse with MHC class II loading compartments. In addition to APCs, other cells of the gastrointestinal tract, such as epithelial cells, express MHC class II molecules and CD74 and act as APCs, which is an unusual trait of the GI tract. To produce a MHC class II molecule that presents an antigen, three MHC class II molecules (heterodimers of an alpha and a beta chain) associate with a CD74 trimer in the ER to form a heterononamer. Soon after the entry of this complex into the endosomal/lysosomal system where antigen processing occurs, CD74 undergoes a sequential degradation by various proteases, including CTSS and CTSL, leaving a small fragment termed CLIP (class-II-associated invariant chain peptide). The removal of CLIP is facilitated by HLA-DM via direct binding to the alpha-beta-CLIP complex so that CLIP is released. HLA-DM stabilizes MHC class II molecules until primary high affinity antigenic peptides are bound. The MHC II molecule bound to a peptide is then transported to the cell membrane surface. In B-cells, the interaction between HLA-DM and MHC class II molecules is regulated by HLA-DO. Primary dendritic cells (DCs) also to express HLA-DO. Lysosomal microenvironment has been implicated in the regulation of antigen loading into MHC II molecules, increased acidification produces increased proteolysis and efficient peptide loading.

Research Articles on HLA-DRB5

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Product Notes

The Human HLA-DRB5 hla-drb5 (Catalog #AAA2880384) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA2880384 ELISA Kit recognizes Human HLA-DRB5. It is sometimes possible for the material contained within the vial of "HLA class II histocompatibility antigen, DR beta 5 chain, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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