Comparison

Mouse Anti-Human CD79 (B29 Ig)

Item no. 20-787-276190
Manufacturer GENWAY
Amount 0.1 mg
Category
Type Antibody
Applications FC, IP, IHC
Clone CB3-1
Specific against Human (Homo sapiens)
Host Mouse
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-25F069
Similar products 20-787-276190
Available
Genway ID:
GWB-25F069
Isotype:
Mouse IgG1
Clone:
CB3-1
Characterization:
To ensure lot-to-lot consistency each batch of monoclonal antibody is tested to conform to characteristics of a standard reference reagent using immunofluorescence staining and analysis on a Becton Dickinson FACScanTM flow cytometer.
Specificity:
Human CD79/B29/IgCD79 is a 23/21 disulfide-linked heterodimer composed of an chain (CD79a/mb-1) and a chain (CD79b/B29) that associates non-covalently with membrane immunoglobulin to form the B cell receptor (BCR) complex. Its expression is restricted to B lymphocytes first appearing on the surface at the pro-B cell stage and remaining through all stages of B cell differentiation prior to plasma cells. Crosslinking of the BCR leads to B cell activation. The monoclonal antibody CB3-1 reacts with the chain of CD79. ^1-4
Working Dilution:
Flow Cytometry: 1 ug/10^6 cells
Warning:
Reagents contain sodium azide which is very toxic if ingested or inhaled. Avoid contact with skin eyes or clothing. Wear eye or face protection when handling. If skin or eye contact occurs wash with copious amounts of water. If ingested or inhaled contact a physician immediately. Sodium azide yields toxic hydrazoic acid under acidic conditions. Dilute azide-containing compounds in running water before discarding to avoid accumulation of potentially explosive deposits in lead or copper plumbing.
Function:
Required in cooperation with CD79B for initiation of the signal transduction cascade activated by binding of antigen to the B-cell antigen receptor complex (BCR) which leads to internalization of the complex trafficking to late endosomes and antigen presentation. Also required for BCR surface expression and for efficient differentiation of pro- and pre-B-cells. Stimulates SYK autophosphorylation and activation. Binds to BLNK bringing BLNK into proximity with SYK and allowing SYK to phosphorylate BLNK. Also interacts with and increases activity of some Src-family tyrosine kinases. Represses BCR signaling during development of immature B cells.
Subunit:
Heterodimer of alpha and beta chains; disulfide-linked. Part of the B-cell antigen receptor complex where the alpha/beta chain heterodimer is non-covalently associated with an antigen-specific membrane-bound surface immunoglobulin of two heavy chains and two light chains. Interacts through its phosphorylated ITAM domain with the SH2 domains of SYK which stimulates SYK autophosphorylation and activation. Also interacts when phosphorylated on Tyr-210 with the SH2 domain of BLNK/SLP65 bringing BLNK into proximity with SYK and allowing SYK to phosphorylate BLNK which is necessary for trafficking of the BCR to late endosomes. Interacts with Src-family tyrosine kinases including FYN and LYN increasing their activity (By similarity).
Subcellular Location:
Cell membrane; Single-pass type I membrane protein. Note=Following antigen binding the BCR has been shown to translocate from detergent-soluble regions of the cell membrane to lipid rafts although signal transduction through the complex can also occur outside lipid rafts (By similarity).
Tissue Specificity:
B-cells.
Ptm:
Phosphorylated on tyrosine serine and threonine residues upon B-cell activation. Phosphorylation of tyrosine residues by Src-family kinases is an early and essential feature of the BCR signaling cascade. The phosphorylated tyrosines serve as docking sites for SH2-domain containing kinases leading to their activation which in turn leads to phosphorylation of downstream targets. Phosphorylation of serine and threonine residues may prevent subsequent tyrosine phosphorylation.
Disease:
Defects in CD79A are a cause of non-Bruton type agammaglobulinemia [MIM:601495]. Agammaglobulinemia is an immunodeficiency disease which results in developmental defects in the maturation pathway of B-cells. Two different mutations one at the splice donor site of intron 2 and the other at the splice acceptor site for exon 3 have been identified. Both mutations give rise to a truncated protein.
Similarity:
Contains 1 Ig-like C2-type (immunoglobulin-like) domain.
Similarity:
Contains 1 ITAM domain. Schlossman S. L. Bloumsell W. Gilks J. M. Harlan C. Kishimoto J. Ritz S. Shaw R. Silverstein T. Springer T. F. Tedder and R. F. Todd eds. 1995. Leukocyte Typing V: White Cell Differentiation Antigens Oxford University Press Oxford. Kishimoto T. A. E. G. von dern Borne S. M. Goyert D. Y. Mason M. Miyasaka L. Moretta K. Okumura S. Shaw T. A. Springer K. Sugamura and H. Zola eds. 1998. Leukocyte Typing VI: White Cell Differentiation Antigens Academic Press New York. Barclay A. N. M. H. Brown S. K. A. Law A. J. McKnight M. G. Tomlinson and P. A. van der Merwe eds. 1997. The Leukocyte Antigens Facts Book 2nd Edition CD79 Section Academic Press New York p. 332. Nakamura T. H. Kubagawa and M. D. Cooper 1992. Proc. Natl. Acad. Sci. USA 89:8522.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0.1 mg
Available: In stock
available

Compare

Add to wishlist

Get an offer

Request delivery time

Ask a technical question

Submit a bulk request

Questions about this Product?
 
Close