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Browse our Xeroderma Pigmentosum, Complementation Group B (XP-B) ELISA Kits

Full name:
Xeroderma Pigmentosum, Complementation Group B ELISA Kits (XP-B)
On www.antibodies-online.com are 0 Xeroderma Pigmentosum, Complementation Group B (XP-B) ELISA Kits from different suppliers available. A total of 0 Xeroderma Pigmentosum, Complementation Group B products are currently listed.
Synonyms:
BTF2, GTF2H, RAD25, TFIIH, XPB
list all ELISA KIts Gene Name GeneID UniProt
Human XP-B XP-B 2071 P19447

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More ELISA Kits for Xeroderma Pigmentosum, Complementation Group B Interaction Partners

Human Xeroderma Pigmentosum, Complementation Group B (XP-B) interaction partners

  1. Transcriptional differences found between various TFIIH subunit variants participate in the phenotypic variability observed among xeroderma pigmentosum, XP associated with Cockayne syndrome, and trichothiodystrophy individuals.

  2. XPB (show GTF2H5 ELISA Kits) and XPD (show ERCC2 ELISA Kits) enrichment at G4 motifs characterizes specific signaling pathways and regulatory pathways associated with specific cancers

  3. findings suggest that benzene exposure may be associated with hypermethylation in ERCC3 (show ERCC3 ELISA Kits), and that genetic variants in EPHX1 (show EPHX1 ELISA Kits) may play an important role in epigenetic changes and hematotoxicity among benzene-exposed workers

  4. The crystal structure of the C-terminal half of the XPB (show GTF2H5 ELISA Kits) subunit of TFIIH (show GTF2H1 ELISA Kits) (residues 494-782) is reported, containing XPB (show GTF2H5 ELISA Kits) helicase domain (HD)2 (show HDAC2 ELISA Kits) and a C-terminal extension which shares structural similarity with RIG-I (show DDX58 ELISA Kits).

  5. results identify the ARCH domain of XPD (show ERCC2 ELISA Kits) as a platform for the recruitment of CAK (show CCNH ELISA Kits) and as a molecular switch that might control TFIIH (show GTF2H1 ELISA Kits) composition and play a role in conversion of TFIIH (show GTF2H1 ELISA Kits) from a factor active in transcription to a factor involved in DNA repair

  6. XPB (show GTF2H5 ELISA Kits) and XPD (show ERCC2 ELISA Kits) helicases differentially regulate TFIIH (show GTF2H1 ELISA Kits) compositional change during nucleotide excision repair.

  7. Phenotype-specific adverse effects of XPD (show ERCC2 ELISA Kits) mutations on human prenatal development implicate impairment of TFIIH (show GTF2H1 ELISA Kits)-mediated functions in placenta.

  8. reduction in ERCC3 (show ERCC3 ELISA Kits) by siRNA interference in human melanocytes in vitro reduced their tyrosinase (show TYR ELISA Kits) production ability

  9. high expression of ERCC1 (show ERCC1 ELISA Kits), XPB (show GTF2H5 ELISA Kits) and ILF3 (show MMP4 ELISA Kits) was observed in human epithelial ovarian cancer

  10. These results indicated that persistent HBV infection might trigger NER (show NR1H2 ELISA Kits) impairment in part through upregulation of miR (show MLXIP ELISA Kits)-192, which suppressed the levels of ERCC3 (show ERCC3 ELISA Kits) and ERCC4 (show ERCC4 ELISA Kits).

Xeroderma Pigmentosum, Complementation Group B (XP-B) Antigen Profile

Antigen Summary

ERCC3 is an ATP-dependent DNA helicase that functions in nucleotide excision repair and complements xeroderma pigmentosum group B mutations. It also is the 89 kDa subunit of basal transcription factor 2 (TFIIH) and thus functions in class II transcription.

Alternative names and synonyms associated with Xeroderma Pigmentosum, Complementation Group B (XP-B)

  • excision repair cross-complementing rodent repair deficiency, complementation group 3 (ERCC3) Elisa Kit
  • BTF2 Elisa Kit
  • GTF2H Elisa Kit
  • RAD25 Elisa Kit
  • TFIIH Elisa Kit
  • XPB Elisa Kit

Protein level used designations for XP-B

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 protein , xeroderma pigmentosum, complementation group B

GENE ID SPECIES
2071 Homo sapiens
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