EIF2B2 ELISA Kit for Human(Homo sapiens) | EIAab.comEIF2B2 ELISA Kit for Human(Homo sapiens)

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Index > Protein center > EIF2B2(Gene name) > Human

EIF2B2 (Gene name),

Translation initiation factor eIF-2B subunit beta (Protein name ), EI2BB_HUMAN from NCBI database.

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General Annotation

Antigen Annotation

Predicted Eptitope

Vaild Sequence

Related Databases

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Gene name:

EIF2B2(EIF2BB);

Protein name:

Translation initiation factor eIF-2B subunit beta;

Alternative:

S20III15;S20I15;eIF-2B GDP-GTP exchange factor subunit beta;

Organism:

Human (Homo sapiens).

General Annotation

Sub Unit:

Complex of five different subunits; alpha, beta, gamma, delta and epsilon.

Function:

Catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP.

Subcellular Location:

N/A

Protein Attributes:

Sequence length:

351

Sequence:

50:

100:

150:

200:

250:

300:

350:

351:

3D Structure:

N/A

Predicted Eptitope:

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Vaild Sequence:

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Related Databases

String:

P49770

UniGene:

Hs.409137

Pfam:

PF01008

KEGG:

hsa:8892

STRING:

9606.ENSP00000266126

SMR:

P49770

MIM:

603896

Uniprot:

P49770

FOR

ELISA Kit for Human Translation initiation factor eIF-2B subunit beta

CLIA Kit for Human Translation initiation factor eIF-2B subunit beta

Polyclonal Antibody for Human Translation initiation factor eIF-2B subunit beta

Monoclonal Antibody for Human Translation initiation factor eIF-2B subunit beta

Protein for Human Translation initiation factor eIF-2B subunit beta

R&D Technical Data

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Precision

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Recovery

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

Linearity

For more information, please refer to the manual,Or contact our technical support: tech@eiaab.com.

References

1.

Yu W. , Sarginson J. , Gibbs R.A.
Submitted (1997-11) to the EMBL/GenBank/DDBJ databases

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]
tissue: Brain.
2.

"Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease."
Sherrington R. , Rogaev E.I. , Liang Y. , Rogaeva E.A. , Levesque G. , Ikeda M. , Chi H. , Lin C. , Li G. , Holman K. , Tsuda T. , Mar L. , Foncin J.-F. , Bruni A.C. , Montesi M.P. , Sorbi S. , Rainero I. , Pinessi L. , more...
Nature375:754-760(1995) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA]
tissue: Brain.
3.

"The DNA sequence and analysis of human chromosome 14."
Heilig R. , Eckenberg R. , Petit J.-L. , Fonknechten N. , Da Silva C. , Cattolico L. , Levy M. , Barbe V. , De Berardinis V. , Ureta-Vidal A. , Pelletier E. , Vico V. , Anthouard V. , Rowen L. , Madan A. , Qin S. , Sun H. , Du H. , more...
Nature421:601-607(2003) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
4.

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]
tissue: Lung.
5.

"Initial characterization of the human central proteome."
Burkard T.R. , Planyavsky M. , Kaupe I. , Breitwieser F.P. , Buerckstuemmer T. , Bennett K.L. , Superti-Furga G. , Colinge J.
BMC Syst. Biol.5:17-17(2011) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]
6.

"N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB."
Van Damme P. , Lasa M. , Polevoda B. , Gazquez C. , Elosegui-Artola A. , Kim D.S. , De Juan-Pardo E. , Demeyer K. , Hole K. , Larrea E. , Timmerman E. , Prieto J. , Arnesen T. , Sherman F. , Gevaert K. , Aldabe R.
Proc. Natl. Acad. Sci. U.S.A.109:12449-12454(2012) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]
7.

"Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter."
Leegwater P.A.J. , Vermeulen G. , Koenst A.A.M. , Naidu S. , Mulders J. , Visser A. , Kersbergen P. , Mobach D. , Fonds D. , van Berkel C.G.M. , Lemmers R.J.L.F. , Frants R.R. , Oudejans C.B.M. , Schutgens R.B.H. , Pronk J.C. , van der Knaap M.S.
Nat. Genet.29:383-388(2001) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS VWM GLY-213; ARG-273; ASP-316 AND VAL-329
8.

"Ovarian failure related to eukaryotic initiation factor 2B mutations."
Fogli A. , Rodriguez D. , Eymard-Pierre E. , Bouhour F. , Labauge P. , Meaney B.F. , Zeesman S. , Kaneski C.R. , Schiffmann R. , Boespflug-Tanguy O.
Am. J. Hum. Genet.72:1544-1550(2003) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS VWM PHE-171 AND GLY-213
9.

"Identification of ten novel mutations in patients with eIF2B-related disorders."
Ohlenbusch A. , Henneke M. , Brockmann K. , Goerg M. , Hanefeld F. , Kohlschutter A. , Gartner J.
Hum. Mutat.25:411-411(2005) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS VWM PHE-171; SER-196; VAL-200 AND GLY-213
10.

"Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5."
Matsukawa T. , Wang X. , Liu R. , Wortham N.C. , Onuki Y. , Kubota A. , Hida A. , Kowa H. , Fukuda Y. , Ishiura H. , Mitsui J. , Takahashi Y. , Aoki S. , Takizawa S. , Shimizu J. , Goto J. , Proud C.G. , Tsuji S.
Neurogenetics12:259-261(2011) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT VWM GLU-85
11.

"Vanishing white matter disease caused by EIF2B2 mutation with the presentation of an adrenoleukodystrophy phenotype."
Alsalem A. , Shaheen R. , Alkuraya F.S.
Gene496:141-143(2012) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT VWM TYR-268
12.

"Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course."
Sambati L. , Agati R. , Bacci A. , Bianchi S. , Capellari S.
Neurol. Sci.34:1235-1238(2013) [PubMed] [Europe PMC] [Abstract]

[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT VWM GLY-213

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