CD179b rabbit pAb

CD179b rabbit pAb

AO-06-ES1898-50

CD179b rabbit pAb 50μL

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€299.00
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Antibody Product Overview

ELK.NoES1898
Product nameCD179b rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;ELISA
Other nameIGLL1; IGL1; Immunoglobulin lambda-like polypeptide 1; CD179 antigen-like family member B; Ig lambda-5; Immunoglobulin omega polypeptide; Immunoglobulin-related protein 14.1; CD antigen CD179b; IGLC1; Ig lambda-1 chain C regions; IGLC2; Ig
Size50μL
Unit price ($)148
Human gene ID3543
Human Swiss-ProtP15814/P0CG04/P0CG05/P0CG06/P0CF74/A0M8Q6
SourceRabbit
IsotypeIgG
TargetCD179b
Fields>>Primary immunodeficiency
Gene nameIGLL1/IGLC1/IGLC2/IGLC3/IGLC6/IGLC7
Protein nameImmunoglobulin lambda-like polypeptide 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-Prot
Mouse Swiss link
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human CD179b. AA range:26-75
SpecificityCD179b Polyclonal Antibody detects endogenous levels of CD179b 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)23kD
Backgroundimmunoglobulin lambda like polypeptide 1(IGLL1) Homo sapiens The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in IGLL1 are a cause of autosomal recessive non-Bruton type agammaglobulinemia [MIM:601495]. It is characterized by agammaglobulinemia and markedly reduced numbers of B cells.,online information:IGLL1 mutation db,similarity:Contains 1 Ig-like C1-type (immunoglobulin-like) domain.,subunit:Associates non-covalently with VPREB1.,tissue specificity:Expressed only in pre-B-cells and a special B-cell line (which is surface Ig negative).,
Subcellular locationEndoplasmic reticulum . Secreted . In pre-B cells, localizes predominantly to the endoplasmic reticulum. .
ExpressionExpressed only in pre-B-cells and a special B-cell line (which is surface Ig negative).

Additional Images

Image 1
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Western Blot analysis of various cells using CD179b Polyclonal Antibody diluted at 1:1000
Image 2
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Western blot analysis of lysate from HeLa cells, using CD179b antibody.
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: AO-06-ES1898-50
: 10 Items
Hurry! only 10 items left in stock.

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