Recombinant Human ERCC5 Protein (Leu778-Ala986), His tagged
| Cat.No. : | ERCC5-2298H |
| Product Overview : | Recombinant human ERCC5 (Leu778-Ala986) protein fused with His tag was expressed in E. coli. |
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| Species : | Human |
| Source : | E.coli |
| Tag : | His |
| Protein Length : | Leu778-Ala986 |
| Description : | Single-stranded structure-specific DNA endonuclease involved in DNA excision repair. Makes the 3'incision in DNA nucleotide excision repair (NER). Acts as a cofactor for a DNA glycosylase that removes oxidized pyrimidines from DNA. May also be involved in transcription-coupled repair of this kind of damage, in transcription by RNA polymerase II, and perhaps in other processes too. |
| Molecular Mass : | 25.07 kDa |
| Purity : | >90 % as determined by SDS-PAGE. |
| Notes : | For research use only. |
| Storage : | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8 centigrade for one week. Store at -20 to -80 centigrade for twelve months from the date of receipt. |
| Storage Buffer : | Supplied as solution form in PBS pH 7.5 or lyophilized from PBS pH 7.5. |
| Reconstitution : | Reconstitute in sterile water for a stock solution. |
| Shipping : | In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise. |
| Gene Name | ERCC5 excision repair cross-complementing rodent repair deficiency, complementation group 5 [ Homo sapiens (human) ] |
| Official Symbol | ERCC5 |
| Synonyms | ERCC5; excision repair cross-complementing rodent repair deficiency, complementation group 5; ERCM2, xeroderma pigmentosum, complementation group G, XPGC; DNA repair protein complementing XP-G cells; Cockayne syndrome; XPG-complementing protein; DNA excision repair protein ERCC-5; xeroderma pigmentosum, complementation group G; XPG; UVDR; XPGC; COFS3; ERCM2; |
| Gene ID | 2073 |
| mRNA Refseq | NM_000123 |
| Protein Refseq | NP_000114 |
| MIM | 133530 |
| UniProt ID | P28715 |
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Not For Human Consumption!
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