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EI2BB Polyclonal Antibody
EI2BB Polyclonal Antibody
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EI2BB Polyclonal Antibody
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经销商客户: ¥214.5
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Target:EI2BB

Fields:Herpes simplex virus 1 infection

Gene Name:EIF2B2 EIF2BB

Protein Name:Translation initiation factor eIF-2B subunit beta (S20I15) (S20III15) (eIF-2B GDP-GTP exchange factor subunit beta)

Human Gene Id:8892

Human Swiss Prot No:P49770

Mouse Swiss Prot No:Q99LD9

Rat Swiss Prot No:Q62818

Immunogen:Synthesized peptide derived from human protein . at AA range: 50-130

Specificity:EI2BB Polyclonal Antibody detects endogenous levels of protein.

Formulation:Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500-2000 ELISA 1:5000-20000

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Observed Band(KD):38kD

Background: This gene encodes the beta subunit of eukaryotic initiation factor-2B (EIF2B). EIF2B is involved in protein synthesis and exchanges GDP and GTP for its activation and deactivation. [provided by RefSeq, Aug 2011],

Function:disease:Defects in EIF2B2 are a cause of leukodystrophy with vanishing white matter (VWM) [MIM:603896]. VWM is a leukodystrophy that occurs mainly in children. Neurological signs include progressive cerebellar ataxia, spasticity, inconstant optic atrophy and relatively preserved mental abilities. The disease is chronic-progressive with, in most individuals, additional episodes of rapid deterioration following febrile infections or minor head trauma. While childhood onset is the most common form of the disorder, some severe forms are apparent at birth. A severe, early-onset form seen among the Cree and Chippewayan populations of Quebec and Manitoba is called Cree leukoencephalopathy. Milder forms may not become evident until adolescence or adulthood. Some females with milder forms of the disease who survive to adolescence exhibit ovarian dysfunction. This variant of the disorder is called

Subcellular Location:cytoplasm,cytosol,eukaryotic translation initiation factor 2B complex,

Expression: Brain,Lung,Placenta,

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