XPB Mouse anti-Human, Clone: OTI6H8, Invitrogen
Mouse Monoclonal Antibody
Manufacturer: Invitrogen MA527133
DescriptionThe 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.
|PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3|
|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|
|-20° C, Avoid Freeze/Thaw Cycles|
|Immunohistochemistry (Paraffin), Western Blot|
|Human recombit protein fragment corresponding to amino acids 191-436 of ERCC3 produced in E.coli|
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