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Browse our DNA Repair Protein Complementing XP-G Cells (ERCC5) ELISA Kits

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DNA Repair Protein Complementing XP-G Cells ELISA Kits (ERCC5)
On www.antibodies-online.com are 9 DNA Repair Protein Complementing XP-G Cells (ERCC5) ELISA Kits from 5 different suppliers available. Additionally we are shipping DNA Repair Protein Complementing XP-G Cells Antibodies (92) and DNA Repair Protein Complementing XP-G Cells Proteins (5) and many more products for this protein. A total of 112 DNA Repair Protein Complementing XP-G Cells products are currently listed.
Synonyms:
cofs3, ercm2, uvdr, Xpg, xpgc
list all ELISA KIts Gene Name GeneID UniProt
ERCC5 2073 P28715
ERCC5 22592  
Rat ERCC5 ERCC5 301382  

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DNA Repair Protein Complementing XP-G Cells (ERCC5) ELISA Kits by Reactivity

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Human DNA Repair Protein Complementing XP-G Cells (ERCC5) interaction partners

  1. The ERCC5 rs751402 gene polymorphism may influence the susceptibility to gastric cancer in the Chinese population.

  2. we found that XPG rs2094258, rs751402, and rs17655 do not influence the development of breast cancer in a Chinese population

  3. The results from this meta-analysis indicate that the XPG gene Asp1104His polymorphism is associated with lung cancer risk, especially in Asians.

  4. ). In conclusion, we suggest that the rs2094258 and rs751402 polymorphisms of ERCC5 are not connected to the development of this disease under codominant, dominant, and recessive models.

  5. The ERCC5 promoter polymorphisms at -763 and +25 may be important functional variants and predictors of clinical outcome of advanced colorectal cancer patients who received oxaliplatin chemotherapy.

  6. our study suggests that the rs17655 polymorphism in XPG is associated with an increased risk of gastric cancer. The results of our findings should be further validated by further large sample size studies

  7. we suggest that the ERCC5 rs751402 polymorphism is associated with development of gastric cancer

  8. ERCC5 single nucleotide polymorphism rs751402 is associated with breast cancer characteristics and risk in the Han population of northwest China.

  9. The results indicate that XPG rs873601G>A polymorphism may be associated with the risk of stomach cancer.

  10. The purpose of this study was to assess the previously reported inconsistent association of polymorphisms in ERCC1 (show ERCC1 ELISA Kits) (rs11615, rs3212986), ERCC2 (show ERCC2 ELISA Kits) (rs13181, rs1799793, rs238406), and ERCC5 (rs17655) with the development of brain tumors.

Mouse (Murine) DNA Repair Protein Complementing XP-G Cells (ERCC5) interaction partners

  1. HIghlighted in this study is the crucial role of XPG's interactions with TFIIH for proper nucleotide excision repair

  2. XPG gene expression can be influenced by an epigenetic mechanism. Restoration of NER (show NR1H2 ELISA Kits) activity through XPG gene transfer or treatment with demethylating agents restored sensitivity to nemorubicin.

  3. introduced a point mutation into the XPG gene which inactivates the nuclease (show DCLRE1C ELISA Kits) catalytic site but leaves the remainder of the protein intact. The mutant mice are hypersensitive to UV irradiation.

  4. Results suggest that the Cockayne syndrome phenotype results from C-terminal truncations in the XPG (xeroderma pigmentosum) gene in mice and humans.

DNA Repair Protein Complementing XP-G Cells (ERCC5) Antigen Profile

Antigen Summary

This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene.

Alternative names and synonyms associated with DNA Repair Protein Complementing XP-G Cells (ERCC5)

  • excision repair cross-complementing rodent repair deficiency, complementation group 5 (ERCC5) Elisa Kit
  • excision repair cross-complementing rodent repair deficiency, complementation group 5 (ercc5) Elisa Kit
  • excision repair cross-complementing rodent repair deficiency, complementation group 5 (Ercc5) Elisa Kit
  • excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G (Cockayne syndrome)) (ERCC5) Elisa Kit
  • cofs3 Elisa Kit
  • ercm2 Elisa Kit
  • uvdr Elisa Kit
  • Xpg Elisa Kit
  • xpgc Elisa Kit

Protein level used designations for ERCC5

DNA repair protein complementing XP-G cells , excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G (Cockayne syndrome)) , DNA excision repair protein ERCC-5 , XPG-complementing protein , xeroderma pigmentosum, complementation group G , DNA repair protein complementing XP-G cells homolog , DNA-repair protein complementing XP-G cells homolog , XP-G related factor , xeroderma pigmentosum group G-complementing protein homolog , XPG

GENE ID SPECIES
100226677 Taeniopygia guttata
2073 Homo sapiens
397963 Xenopus laevis
509602 Bos taurus
22592 Mus musculus
301382 Rattus norvegicus
428019 Gallus gallus
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