recommended for detection of Ser 280 phosphorylated Chk1 of human origin by WB and IP
Modification
Phosphoralated
Modification Notes
Cell cycle events are regulated by the sequential activation and deactivation of cyclin dependent kinases (Cdks) and by proteolysis of cyclins (1). 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 phospho-rylating Cdc25C in response to DNA damage. Phosphorylation inhibits Cdc25C activity, thereby blocking mitosis (2–5). Cdc25A, Cdc25B and Cdc25C protein tyrosine phosphatases function as mitotic activators by dephosphorylating Cdc2 p34 on regulatory tyrosine residues (6). 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 (3). Chk1 is phosphorylated on Serine 345 (S345) in response to UV, IR and hydroxyurea (HU) (7). Chk1 plays an essential role in the mammalian DNA damage checkpoint, embryonic development, and tumor suppression (7). The phosphorylation of human Chk1 on Ser 280 is thought to be promoted by Akt1 and may lead to mono and/or diubiquitination of Chk1.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIP
WB:1:500~1:2000 IP:1:100~1:500 Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of Ser 280 phosphorylated Chk1 of human origin by WB and IP
Tissue Specificity
recommended for detection of Ser 280 phosphorylated Chk1 of human origin by WB and IP