IL-2Rγ rabbit pAb

IL-2Rγ rabbit pAb

AO-06-ES4110-100

IL-2Rγ rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4110
Product nameIL-2Rγ rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;ELISA
Other nameIL2RG; Cytokine receptor common subunit gamma; Interleukin-2 receptor subunit gamma; IL-2 receptor subunit gamma; IL-2R subunit gamma; IL-2RG; gammaC; p64; CD132
Size100μL
Unit price ($)248
Human gene ID3561
Human Swiss-ProtP31785
SourceRabbit
IsotypeIgG
TargetIL-2Rγ
Fields>>Cytokine-cytokine receptor interaction;>>Viral protein interaction with cytokine and cytokine receptor;>>Endocytosis;>>PI3K-Akt signaling pathway;>>JAK-STAT signaling pathway;>>Th1 and Th2 cell differentiation;>>Th17 cell differentiation;>>Measles;>>Human T-cell leukemia virus 1 infection;>>Pathways in cancer;>>Inflammatory bowel disease;>>Primary immunodeficiency
Gene nameIL2RG
Protein nameCytokine receptor common subunit gamma
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtP34902
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 IL2RG. AA range:101-150
SpecificityIL-2Rγ Polyclonal Antibody detects endogenous levels of IL-2Rγ protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/20000. 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)40kD
BackgroundThe protein encoded by this gene is an important signaling component of many interleukin receptors, including those of interleukin -2, -4, -7 and -21, and is thus referred to as the common gamma chain. Mutations in this gene cause X-linked severe combined immunodeficiency (XSCID), as well as X-linked combined immunodeficiency (XCID), a less severe immunodeficiency disorder. [provided by RefSeq, Mar 2010],
Functiondisease:Defects in IL2RG are the cause of X-linked combined immunodeficiency (XCID) [MIM:312863]. XCID is a less severe form of X-linked immunodeficiency with a less severe degree of deficiency in cellular and humoral immunity than that seen in XSCID.,disease:Defects in IL2RG are the cause of X-linked severe combined immunodeficiency (XSCID) [MIM:300400]; also known as agammaglobulinemia Swiss type. SCID refers to a genetically and clinically heterogeneous group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. Patients with SCID present in infancy with recurrent, persistent infections by opportunistic organisms. The common characteristic of all types of SCID is absence of T-cell-mediated cellular immunity due to a defect in T-cell development.,domain:The box 1 motif is required for JAK inte
Subcellular locationCell membrane ; Single-pass type I membrane protein . Cell surface .
ExpressionB-cell,Liver,Peripheral blood,

Additional Images

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Western Blot analysis of K562 cells using IL-2Rγ Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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Western blot analysis of lysate from K562 cells, using IL2RG Antibody.
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: AO-06-ES4110-100
: 10 Items
Hurry! only 10 items left in stock.

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