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- rabbit polyclonal IgG, 200 µg/ml
- epitope corresponding to amino acids 1-476 representing full length Chk1 of human origin
- recommended for detection of Chk1 of mouse, rat, human and Xenopus origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, bovine and porcine
- agarose conjugate for IP studies, sc-7898 AC, 500 µg/0.25 ml agarose
- fluorescein (sc-7898 FITC) and rhodamine (sc-7898 TRITC) conjugates for immunofluorescence, 200 µg/ml
- Alexa Fluor® 405 (sc-7898 AF405), Alexa Fluor® 488 (sc-7898 AF488) and Alexa Fluor® 647 (sc-7898 AF647) conjugates for immunofluorescence; 100 µg/2 ml
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Ordering InformationProduct Citations
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| Species |
Gene Name |
Gene ID |
Chromosome Location |
Isoform (mRNA) Accession # |
Protein Accession # |
OMIM™ Number |
| Human |
CHEK1 |
1111 |
11q24.2 |
NM_001274 |
O14757
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603078 |
| Mouse |
Chek1 |
12649 |
9 A4 |
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O35280
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N/A |
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Chk1 Background Information Cell cycle events are regulated by the sequential activation and deactivation of cyclin dependent kinases (Cdks) and by proteolysis of cyclins. Chk1 and Chk2 are involved in these processes as regulators of Cdks. Chk1 and Chk2 both function as essential components in the G2 DNA damage checkpoint by phosphorylating Cdc25C in response to DNA damage. Phosphorylation inhibits Cdc25C activity, thereby blocking mitosis. Cdc25A, Cdc25B and Cdc25C protein tyrosine phosphatases function as mitotic activators by dephosphorylating Cdc2 p34 on regulatory tyrosine residues. It has also been shown that Chk1 can phosphorylate Wee1 in vitro, providing evidence that the hyperphosphorylated form of Wee1, seen in cells delayed by Chk1 overexpression, is due to phosphorylation by Chk1.
| Chk1 (FL-476) Product Citations |
See how others have used Chk1 (FL-476): sc-7898 antibody and or Chk1 (FL-476) antibody conjugates.
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Chk1 (FL-476)
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Chk1 (FL-476): sc-7898. Western blot analysis of Chk1 expression in HeLa (A), K-562 (B) and NIH/3T3 (C) whole cell lysates.
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