![XPG antibody [C2C3], C-term](https://www.genetex.com/upload/website/prouct_img/normal/GTX110609/GTX110609_40471_WB_w_23060500_694.webp)
GTX110609
XPG antibody [C2C3], C-term
Cannot supply to this region.
- SKU:
- GTX110609
- Additional Names:
- ERCC excision repair 5, endonuclease , COFS3 , ERCC5-201 , ERCM2 , UVDR , XPG , XPGC
- Application:
- WB
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 1% BSA, 20% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Recombinant protein encompassing a sequence within the C-terminus region of human XPG. The exact sequence is proprietary.
- Clone:
- C2C3
- Uniprot:
- P28715
- Synonyms:
- COFS3;DNA excision repair protein ERCC-5;DNA repair protein complementing XP-G cells;ERCC5-201;ERCM2;excision repair cross-complementation group 5;excision repair cross-complementing rodent repair deficiency, complementation group 5;UVDR;Xeroderma pigmentosum group G-complementing protein;xeroderma pigmentosum, complementation group G;XPG;XPG-complementing protein;XPGC
- Extra Details:
- 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]
- Shipping Conditions:
- Blue Ice