| Cat.# |
CB14850
|
| Size |
56
µg / 200
ml |
| Isotype:
|
mouse
monoclonal IgG1
|
| Epitope: |
recombinant human Chk1 protein
|
|
Species
&
specficity:
|
Human,
mouse, & rat Chk1
|
| Storage: |
Store
at -20°C, 4°C for frequent use. Avoid repeated freeze-thaw
cycles.
|
| MW:
|
56
kDa
|
|
Application:
|
WB
|
IP |
IHC
(Paraffin) |
FACS |
|
Dilution:
|
1:1000
|
1:50 |
1:50 |
1:100 |
|
Background:
Checkpoint
kinase 1 (Chk1) is a serine/threonine protein kinase and a key mediator
in the DNA damage-induced checkpoint network1. The key
mission of Chk1 is to relay the checkpoint signals from the proximal
checkpoint kinases of the phosphatidylinositol 3-kinase family,
particularly ATM and ATR, and likely also the newly identified ATX,
which phosphorylate and activate Chk1. The labile Chk1 protein is
largely restricted to S and G2 phases. It is active even in unperturbed
cell cycles, and although it is further activated in response to DNA
damage or stalled replication, this may not require Chk1 dimerization or
autophosphorylation2, 3. Following their activation, Chk1
phosphorylates downstream effectors that further propagate the
checkpoint signaling. Depending on the type of stress, velocity of DNA
damage, and cellular context, this leads to (a) switch to the
stress-induced transcription program (E2F1, Brca1, p53), (b) direct or
indirect initiation of DNA repair (p53), (c) acute delay (degradation of
Cdc25A) and/or sustained block (Cdc25C, p53) of cell cycle progression,
(d) apoptosis (p53, E2F1), and (e) modulation of the chromatin
remodeling pathways (Tlk1/2)4.
References:
1.
Tao, Z. F. & Lin, N. H.: Anticancer Agents Med. Chem.
6:377, 2006.
2.
Lam, M. N. & Rosen, J. M.: Cell
Cycle 3:1355, 2004.
3.
Zhou, B. B. & Sausville, E.A.: Prog
Cell Cycle Res. 5:413, 2003.
4.
Bartes, J. & Lukas, J.: Cancer
Cell 3:421, 2003.
|
|
|

Specific
detection of Chk1 protein in HeLa cell lysate by Western blot analysis
using Chk1
monoclonal
antibody (8C10).
|
|