DNA Repair Protein Complementing XP-G Cells ELISA Kits

5 DNA Repair Protein Complementing XP-G Cells (ERCC5) ELISA Kits from 5 manufacturers are available on www.antibodies-online.com.

Data Quality
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Type
  • 5
    Kit
Antigen
  • 5
Reactivity
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  • 1
Application
  • 5
Method Type
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  • 1
Analytical Method
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Detection Method
  • 5
Plate
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Sample
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5 Products
Pre-coated, Samples: Cell Lysate, Tissue Homogenate
ReactivityHuman
Detection MethodColorimetric, Sandwich ELISA
Detection Range0.31 ng/mL - 20 ng/mL
Order details Cat. No. ABIN417284
$700.00
Plus shipping costs $45.00
Delivery in 13 to 16 Business Days
Pre-coated, Samples: Cell Lysate, Tissue Homogenate
ReactivityHuman
Detection MethodColorimetric, Sandwich ELISA
Detection Range0.156 ng/mL - 10 ng/mL
Order details Cat. No. ABIN1573141
$870.62
Plus shipping costs $45.00
Delivery in 15 to 17 Business Days
ReactivityHuman
Detection MethodColorimetric, Cell ELISA
Detection RangeQualitative
Order details Cat. No. ABIN5648051
$380.00
96 tests
Plus shipping costs $45.00
Delivery in 2 to 3 Business Days
ReactivityMouse (Murine)
Detection MethodColorimetric,
Order details Cat. No. ABIN1130135
$875.60
96 tests
Plus shipping costs $45.00
Delivery in 15 to 18 Business Days
Pre-coated, Samples: Cell Lysate, Tissue Homogenate
ReactivityHuman
Detection MethodColorimetric, Sandwich ELISA
Detection Range0.312 ng/mL - 20 ng/mL
Order details Cat. No. ABIN5660072
$928.46
96 tests
Plus shipping costs $45.00
Delivery in 8 to 12 Business Days
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DNA Repair Protein Complementing XP-G Cells (ERCC5) Antigen Profile

Protein 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)

  • ERCC excision repair 5, endonuclease (ERCC5) antibody
  • excision repair cross-complementation group 5 L homeolog (ercc5.L) antibody
  • excision repair cross-complementing rodent repair deficiency, complementation group 5 (Ercc5) antibody
  • ERCC excision repair 5, endonuclease (Ercc5) antibody
  • cofs3 antibody
  • ercm2 antibody
  • uvdr antibody
  • Xpg antibody
  • xpgc antibody

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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