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EIF2B4, Polyclonal Antibody

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产品名称: EIF2B4, Polyclonal Antibody
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简单介绍

EIF2B4, Polyclonal Antibody


EIF2B4, Polyclonal Antibody  的详细介绍
Product Name

EIF2B4, Polyclonal Antibody

Full Product Name

EIF2B4 Antibody - middle region

Product Gene Name

anti-EIF2B4 antibody

[Similar Products]
Product Synonym Gene Name
EIF2B; EIF-2B; EIF2Bdelta;[Similar Products]
Antibody/Peptide Pairs
EIF2B4 peptide (MBS3245741) is used for blocking the activity of EIF2B4 antibody (MBS3220947)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Immunogen Sequence
Synthetic peptide located within the following region: VKKPERQQVP TRKDYGSKVS LFSHLPQYSR QNSLTQFMSI PSSVIHPAMV
OMIM
603896
3D Structure
ModBase 3D Structure for Q9UI10
Clonality
Polyclonal
Host
Rabbit
Species Reactivity
Human
Purity/Purification
Affinity purified
Form/Format
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Immunogen
The immunogen is a synthetic peptide directed towards the middle region of human EIF2B4
Preparation and Storage
For short term use, store at 2-8 degree C up to 1 week. For long term storage, store at -20 degree C in small aliquots to prevent freeze-thaw cycles.
Other Notes
Small volumes of anti-EIF2B4 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
anti-EIF2B4 antibody
Eukaryotic initiation factor 2B (EIF2B), which is necessary for protein synthesis, is a GTP exchange factor composed of five different subunits. The protein encoded by this gene is the fourth, or delta, subunit. Defects in this gene are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.
Product Categories/Family for anti-EIF2B4 antibody
Polyclonal; Transcription Factor; Disease Related;
Applications Tested/Suitable for anti-EIF2B4 antibody
Western Blot (WB)

Western Blot (WB) of anti-EIF2B4 antibody
Host: Rabbit
Target Name: EIF2B4
Sample Tissue: HCT116 Whole Cell lysates
Antibody Dilution: 1.0ug/ml
anti-EIF2B4 antibody Western Blot (WB) (WB) image
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NCBI/Uniprot data below describe general gene information for EIF2B4. It may not necessarily be applicable to this product.
NCBI GI #
78000158
NCBI GeneID
8890
NCBI Accession #
NP_001029288.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001034116.1 [Other Products]
UniProt Primary Accession #
Q9UI10 [Other Products]
UniProt Related Accession #
Q9UI10[Other Products]
Molecular Weight
57 kDa
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NCBI Official Full Name
translation initiation factor eIF-2B subunit delta isoform 2
NCBI Official Synonym Full Names
eukaryotic translation initiation factor 2B subunit delta
NCBI Official Symbol
EIF2B4  [Similar Products]
NCBI Official Synonym Symbols
EIF2B; EIF-2B; EIF2Bdelta
  [Similar Products]
NCBI Protein Information
translation initiation factor eIF-2B subunit delta
UniProt Protein Name
Translation initiation factor eIF-2B subunit delta
UniProt Synonym Protein Names
eIF-2B GDP-GTP exchange factor subunit delta
Protein Family
Translation initiation factor
UniProt Gene Name
EIF2B4  [Similar Products]
UniProt Synonym Gene Names
EIF2BD  [Similar Products]
UniProt Entry Name
EI2BD_HUMAN
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NCBI Summary for EIF2B4
Eukaryotic initiation factor 2B (EIF2B), which is necessary for protein synthesis, is a GTP exchange factor composed of five different subunits. The protein encoded by this gene is the fourth, or delta, subunit. Defects in this gene are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
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UniProt Comments for EIF2B4
eIF2B-delta: Catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP. Defects in EIF2B4 are a cause of leukodystrophy with vanishing white matter (VWM). 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 *****hood. Some females with milder forms of the disease who survive to adolescence exhibit ovarian dysfunction. This variant of the disorder is called ovarioleukodystrophy. Belongs to the eIF-2B alpha/beta/delta subunits family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Translation initiation; Motility/polarity/chemotaxis; Translation

Chromosomal Location of Human Ortholog: 2p23.3

Cellular Component: eukaryotic translation initiation factor 2B complex; cytoplasm; cytosol

Molecular Function: protein binding; translation initiation factor binding; guanyl-nucleotide exchange factor activity; translation initiation factor activity; S-methyl-5-thioribose-1-phosphate isomerase activity

Biological Process: myelination; response to peptide hormone stimulus; negative regulation of translational initiation; translation; cellular response to stimulus; regulation of translation; cellular protein metabolic process; ovarian follicle development; methionine salvage; response to heat; response to glucose stimulus; translational initiation; gene expression; negative regulation of translation initiation in response to stress; oligodendrocyte development; positive regulation of GTPase activity; regulation of translational initiation

Disease: Leukoencephalopathy With Vanishing White Matter
Research Articles on EIF2B4
1. A novel missense mutation within EIF2B4 is associated with vanishing white matter disease.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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