CD21 rabbit pAb

CD21 rabbit pAb

AO-06-ES4312-100

CD21 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4312
Product nameCD21 rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;IHC;IF;ELISA
Other nameCR2; C3DR; Complement receptor type 2; Cr2; Complement C3d receptor; Epstein-Barr virus receptor; EBV receptor; CD21
Size100μL
Unit price ($)248
Human gene ID1380
Human Swiss-ProtP20023
SourceRabbit
IsotypeIgG
TargetCD21
Fields>>Complement and coagulation cascades;>>Hematopoietic cell lineage;>>B cell receptor signaling pathway;>>Epstein-Barr virus infection
Gene nameCR2
Protein nameComplement receptor type 2
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtP19070
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 the Internal region of human CR2. AA range:381-430
SpecificityCD21 Polyclonal Antibody detects endogenous levels of CD21 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. 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)115kD
BackgroundThis gene encodes a membrane protein, which functions as a receptor for Epstein-Barr virus (EBV) binding on B and T lymphocytes. Genetic variations in this gene are associated with susceptibility to systemic lupus erythematosus type 9 (SLEB9). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009],
Functiondisease:Genetic variations in CR2 are associated with susceptibility to systemic lupus erythematosus type 9 (SLEB9) [MIM:610927]. Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with a complex genetic basis. SLE is an inflammatory, and often febrile multisystemic disorder of connective tissue characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is thought to represent a failure of the regulatory mechanisms of the autoimmune system.,function:Receptor for complement C3Dd, for the Epstein-Barr virus on human B-cells and T-cells and for HNRPU. Participates in B lymphocytes activation.,similarity:Belongs to the receptors of complement activation (RCA) family.,similarity:Contains 15 Sushi (CCP/SCR) domains.,tissue specificity:Mature B-lymphocytes, T-lymphocytes, pharyngeal epithelial cells, astrocytes and follicular dendritic cells
Subcellular locationCell membrane ; Single-pass type I membrane protein.
ExpressionMature B-lymphocytes, T-lymphocytes, pharyngeal epithelial cells, astrocytes and follicular dendritic cells of the spleen.

Additional Images

Image 1
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Western Blot analysis of NIH-3T3, KB cells using CD21 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Western Blot analysis of 3T3 cells using CD21 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 3
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Immunohistochemical analysis of paraffin-embedded human-tonsils, antibody was diluted at 1:100
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: AO-06-ES4312-100
: 10 Produits
Hurry! only 10 items left in stock.

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