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DNA Repair Protein Complementing XP-G Cells (ERCC5) Antibody
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Catalogue No: abx029850
Price:
US$326.25
(Size: 80 µl)
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Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined. [provided by RefSeq].
Research Articles on DNA Repair Protein Complementing XP-G Cells (ERCC5)
| Target | DNA Repair Protein Complementing XP-G Cells (ERCC5) |
| Clonality | Polyclonal |
| Reactivity | Human |
| Tested Applications | ELISA, WB |
| Host | Rabbit |
| Recommended dilutions | WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user. |
| Conjugation | Unconjugated |
| Immunogen | KLH-conjugated synthetic peptide between 1151-1178 amino acids from the C-terminal region of human ERCC5. |
| Isotype | IgG |
| Form | Liquid |
| Purification | Purified through a protein A column, followed by peptide affinity purification. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| UniProt Primary AC | P28715 (UniProt, ExPASy) |
| UniProt Entry Name | ERCC5_HUMAN |
| Gene Symbol | ERCC5 |
| KEGG | hsa:2073 |
| String | 9606.ENSP00000347978 |
| Molecular Weight | Calculated MW: 133 kDa |
| Buffer | PBS containing 0.09% sodium azide. |
| Availability | Shipped within 5-10 working days. |
| Note | THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION. |