CD79a rabbit pAb

CD79a rabbit pAb

AO-06-ES8092-100

CD79a rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES8092
Product nameCD79a rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;ELISA
Other nameCD79A; IGA; MB1; B-cell antigen receptor complex-associated protein alpha chain; Ig-alpha; MB-1 membrane glycoprotein; Membrane-bound immunoglobulin-associated protein; Surface IgM-associated protein; CD antigen CD79a
Size100μL
Unit price ($)248
Human gene ID973
Human Swiss-ProtP11912
SourceRabbit
IsotypeIgG
TargetCD79A
Fields>>B cell receptor signaling pathway;>>Primary immunodeficiency
Gene nameCD79A
Protein nameB-cell antigen receptor complex-associated protein alpha chain
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID12518
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP11911
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human CD79a. AA range:154-203
SpecificityCD79a Polyclonal Antibody detects endogenous levels of CD79a protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)33kD
BackgroundThe B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-alpha protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008],
Functiondisease: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.,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 SY
Subcellular locationCell membrane; Single-pass type I membrane protein. 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. .
ExpressionB-cells.

Additional Images

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Western blot analysis of lysate from NIH/3T3 cells, using CD79a antibody.
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: AO-06-ES8092-100
: 10 Produits
Hurry! only 10 items left in stock.

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