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Anti-phospho-CHK2 (Thr68)(C48-65R)

Anti-phospho-CHK2 (Thr68)(C48-65R)

  • $248.00


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Description :Rabbit Polyclonal Antibody

Species :

Tag :

Expression System:

Sequence :

Specificity :Recognizes the CHK2 protein phosphorylated at threonine 68

Cited Applications :WB, IHC

Cross Reactivity :Human

Host / Isotype / Clone# :Rabbit, IgG

Immunogen :Synthetic phospho-peptide corresponding to amino acid residues surrounding Thr68

Purification :Affinity chromatography

Stability :Store at 4oC (add 0.1% NaN3) for several months, and at -20oC for longer periods. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.

Sample Data :Western blot analysis of extracts from Jurkat cells using CHK2 antibody (lanes 1 and 2) and anti-phospho-CHK2 (Thr68) antibody (lanes 3 and 4).

Sample Data :Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue using anti-phospho-CHK2 (Thr68) antibody.

Scientific Background :CHK2 is a highly conserved tumor suppressor protein that is activated in response to DNA damage in an ATM-dependent manner (1). Activation of CHK2 is dependent on phosphorylation at sites including Thr68 (2). CHK2 controls cell cycle arrest, DNA repair and apoptosis through activation of DNA damage response proteins such as p53 and BRCA1. Expressing wild-type CHK2 leads to increased p53 stabilization after DNA damage, whereas expression of a dominant-negative CHK2 mutant abrogates phosphorylation of p53, leading to decreased stability (3).

References :
1. Matsuoka, S. et al: Linkage of ATM to cell cycle regulation by the Chk2 protein kinase. Science. 1998 Dec 4;282(5395):1893-7.

2. Li J. et al: Regulation of CHK2 by DNA-dependent protein kinase. J Biol Chem. 2005 Mar 25;280(12):12041-50.

3. Chehab NH. et al: Chk2/hCds1 functions as a DNA damage checkpoint in G(1) by stabilizing p53. Genes Dev. 2000 Feb 1;14(3):278-88.

Product Sheets (By Lot #) :

J1178-18.pdf

Research Areas :Cancer, Cell Cycle, Ser/Thr Kinases, Cancer, Cell Cycle, Ser/Thr Kinases