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eIF2Bγ Rabbit pAb

-YT1505

Catalog: YT1505
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

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Main Information
Target

eIF2Bγ

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

WB, ELISA

MW

50kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; ELISA 1:5000; Not yet tested in other applications.
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
eIF2Bγ Polyclonal Antibody detects endogenous levels of eIF2Bγ protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
50kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from eIF2Bγ . at AA range: 240-320
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Specificity:
eIF2Bγ Polyclonal Antibody detects endogenous levels of eIF2Bγ protein.
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Gene Name:
EIF2B3
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Protein Name:
Translation initiation factor eIF-2B subunit gamma
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Other Name:
EIF2B3 ;
Translation initiation factor eIF-2B subunit gamma ;
eIF-2B GDP-GTP exchange factor subunit gamma
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Database Link:
Organism Gene ID SwissProt
Human 8891; Q9NR50;
Background:
The protein encoded by this gene is one of the subunits of initiation factor eIF2B, which catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP. It has also been found to function as a cofactor of hepatitis C virus internal ribosome entry site-mediated translation. Mutations in this gene have been associated with leukodystrophy with vanishing white matter. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009],
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Function:
Alternative products:Experimental confirmation may be lacking for some isoforms,Disease:Defects in EIF2B3 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 ovarioleukodystrophy.,Function:Catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP.,similarity:Belongs to the EIF-2B gamma/epsilon subunits family.,subunit:Complex of five different subunits; alpha, beta, gamma, delta and epsilon.,
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Cellular Localization:
cytoplasm,cytosol,eukaryotic translation initiation factor 2B complex,
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Tissue Expression:
Blood,Hepatoma,Lymph node,Mammary gland,
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Research Areas:
>>Herpes simplex virus 1 infection
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Catalog: YT1505
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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