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antibody from antibodies-online
Targeting: ERCC2
EM9, MAG, MGC102762, MGC126218, MGC126219, XPD
ImmunohistochemistryAntibody data
- Antibody Data
- Antigen structure
- References [9]
- Comments [0]
- Validations [0]
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- Product number
- ABIN966088 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (ERCC2) (C-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to C-terminal residues of human ERCC2(TFIIH basal transcription factor complex helicase subunit)
- Description
- Purified by antigen-specific affinity chromatography.
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Epitope
- C-Term
- Vial size
- 0.1 mg
- Storage
- -20°C
Submitted references Modulation of nucleotide excision repair capacity by XPD polymorphisms in lung cancer patients.
Associations between ERCC2 polymorphisms and gliomas.
Reconstitution of the transcription factor TFIIH: assignment of functions for the three enzymatic subunits, XPB, XPD, and cdk7.
Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH.
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.
Human xeroderma pigmentosum group D gene encodes a DNA helicase.
Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.
ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3.
Spitz MR, Wu X, Wang Y, Wang LE, Shete S, Amos CI, Guo Z, Lei L, Mohrenweiser H, Wei Q
Cancer research 2001 Feb 15;61(4):1354-7
Cancer research 2001 Feb 15;61(4):1354-7
Associations between ERCC2 polymorphisms and gliomas.
Caggana M, Kilgallen J, Conroy JM, Wiencke JK, Kelsey KT, Miike R, Chen P, Wrensch MR
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2001 Apr;10(4):355-60
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2001 Apr;10(4):355-60
Reconstitution of the transcription factor TFIIH: assignment of functions for the three enzymatic subunits, XPB, XPD, and cdk7.
Tirode F, Busso D, Coin F, Egly JM
Molecular cell 1999 Jan;3(1):87-95
Molecular cell 1999 Jan;3(1):87-95
Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH.
Coin F, Marinoni JC, Rodolfo C, Fribourg S, Pedrini AM, Egly JM
Nature genetics 1998 Oct;20(2):184-8
Nature genetics 1998 Oct;20(2):184-8
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
Taylor EM, Broughton BC, Botta E, Stefanini M, Sarasin A, Jaspers NG, Fawcett H, Harcourt SA, Arlett CF, Lehmann AR
Proceedings of the National Academy of Sciences of the United States of America 1997 Aug 5;94(16):8658-63
Proceedings of the National Academy of Sciences of the United States of America 1997 Aug 5;94(16):8658-63
Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.
Takayama K, Salazar EP, Lehmann A, Stefanini M, Thompson LH, Weber CA
Cancer research 1995 Dec 1;55(23):5656-63
Cancer research 1995 Dec 1;55(23):5656-63
Human xeroderma pigmentosum group D gene encodes a DNA helicase.
Sung P, Bailly V, Weber C, Thompson LH, Prakash L, Prakash S
Nature 1993 Oct 28;365(6449):852-5
Nature 1993 Oct 28;365(6449):852-5
Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.
Flejter WL, McDaniel LD, Johns D, Friedberg EC, Schultz RA
Proceedings of the National Academy of Sciences of the United States of America 1992 Jan 1;89(1):261-5
Proceedings of the National Academy of Sciences of the United States of America 1992 Jan 1;89(1):261-5
ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3.
Weber CA, Salazar EP, Stewart SA, Thompson LH
The EMBO journal 1990 May;9(5):1437-47
The EMBO journal 1990 May;9(5):1437-47
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