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XPB Mouse anti-Human, Clone: OTI6H8, Invitrogen™

Mouse Monoclonal Antibody

Manufacturer:  Invitrogen MA527133

Catalog No. PIMA527133


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Description

Description

The human XPB DNA helicase is a subunit of the DNA repair/basal transcription factor TFIIH, and is involved in early steps of the nucleotide excision repair (NER) pathway. Two distinct clinical phenotypes, xeroderma pigmentosum associated with Cockayne ft.s syndrome (XP/CS) and trichothiodystrophy (TTD), can be due to mutations in the XPB gene.
Specifications

Specifications

XPB
Monoclonal
1 mg/mL
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3
P19447
BTF2, GTF2H, RAD25, TFIIH, XPB, BTF2 p89, DNA excision repair protein ERCC-3, DNA repair protein complementing XP-B cells, TFIIH 89 kDa subunit, TFIIH basal transcription factor complex 89 kDa subunit, TFIIH basal transcription factor complex helicase XPB subunit, TFIIH p89, basic transcription factor 2 89 kDa subunit, xeroderma pigmentosum group B complementing, xeroderma pigmentosum group B-complementing protein, xeroderma pigmentosum, complementation group B
Mouse
IgG1
100 μL
-20° C, Avoid Freeze/Thaw Cycles
Primary
2071
Immunohistochemistry (Paraffin), Western Blot
OTI6H8
Unconjugated
ERCC3
Liquid
ERCC3
Human recombit protein fragment corresponding to amino acids 191-436 of ERCC3 produced in E.coli
Affinity Chromatography
RUO
Antibody
Monoclonal
Human
Documents
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