Product Name
Chk2 (CHEK2), Blocking Peptide
Full Product Name
Chk2 Peptide
Product Synonym Names
CDS1; CHK2; LFS2; RAD53; hCds1; HuCds1; PP1425; CDS1; CHK2 checkpoint homolog; Hucds1; CHK2 checkpoint homolog (S. pombe)
Product Gene Name
CHEK2 blocking peptide
[Similar Products]
Chk2 peptide (MBS153136) is used for blocking the activity of Chk2 antibody (MBS151546)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
OMIM
gene+phenotype 609265
3D Structure
ModBase 3D Structure for O96017
Concentration
200 ug/mL (lot specific)
Buffer
PBS pH 7.2 (10 mM NaH2PO4, 10 mM Na2HPO4, 130 mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide
Location
17 amino amino terminus of human Chk2.
Preparation and Storage
Store Chk2 peptide at -20 degree C, stable for one year.
Other Notes
Small volumes of CHEK2 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for CHEK2 blocking peptide
Blocking (BL)
Application Notes for CHEK2 blocking peptide
Chk2 peptide is used for blocking the activity of Chk2 antibody.
NCBI/Uniprot data below describe general gene information for CHEK2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_009125
[Other Products]
NCBI GenBank Nucleotide #
NM_007194.3
[Other Products]
UniProt Primary Accession #
O96017
[Other Products]
UniProt Secondary Accession #
Q6QA03; Q6QA04; Q6QA05; Q6QA06; Q6QA07; Q6QA08; Q6QA10; A8K3Y9; B7ZBF3; B7ZBF4; B7ZBF5[Other Products]
UniProt Related Accession #
O96017[Other Products]
Molecular Weight
36,157 Da
NCBI Official Full Name
serine/threonine-protein kinase Chk2 isoform a
NCBI Official Synonym Full Names
checkpoint kinase 2
NCBI Official Symbol
CHEK2 [Similar Products]
NCBI Official Synonym Symbols
CDS1; CHK2; LFS2; RAD53; hCds1; HuCds1; PP1425
[Similar Products]
NCBI Protein Information
serine/threonine-protein kinase Chk2; cds1 homolog; CHK2 checkpoint homolog; checkpoint-like protein CHK2
UniProt Protein Name
Serine/threonine-protein kinase Chk2
UniProt Synonym Protein Names
CHK2 checkpoint homolog; Cds1 homolog; Hucds1; hCds1; Checkpoint kinase 2
Protein Family
Serine/threonine-protein kinase
UniProt Gene Name
CHEK2 [Similar Products]
UniProt Synonym Gene Names
CDS1; CHK2; RAD53; Hucds1; hCds1 [Similar Products]
UniProt Entry Name
CHK2_HUMAN
NCBI Summary for CHEK2
In response to DNA damage and replication blocks, cell cycle progression is halted through the control of critical cell cycle regulators. The protein encoded by this gene is a cell cycle checkpoint regulator and putative tumor suppressor. It contains a forkhead-associated protein interaction domain essential for activation in response to DNA damage and is rapidly phosphorylated in response to replication blocks and DNA damage. When activated, the encoded protein is known to inhibit CDC25C phosphatase, preventing entry into mitosis, and has been shown to stabilize the tumor suppressor protein p53, leading to cell cycle arrest in G1. In addition, this protein interacts with and phosphorylates BRCA1, allowing BRCA1 to restore survival after DNA damage. Mutations in this gene have been linked with Li-Fraumeni syndrome, a highly penetrant familial cancer phenotype usually associated with inherited mutations in TP53. Also, mutations in this gene are thought to confer a predisposition to sarcomas, breast cancer, and brain tumors. This nuclear protein is a member of the CDS1 subfamily of serine/threonine protein kinases. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
UniProt Comments for CHEK2
Chk2: a CAMK protein kinase of the Rad53 family. A cell cycle checkpoint regulator and putative tumor suppressor. It contains a forkhead-associated protein interaction domain essential for activation in response to DNA damage and is rapidly phosphorylated in response to replication blocks and DNA damage. Phosphorylates and inhibits CDC25C, preventing entry into mitosis, p53, leading to cell cycle arrest in G1, and BRCA1, restoring survival after DNA damage. Twelve splice variant isoforms have been described for human Chk2. LOF mutants cause Li-Fraumeni syndrome, a highly penetrant familial cancer phenotype also caused by p53 mutations. Familial mutations also associated with prostate and breast cancer, and mutations also seen in a variety of sporadic cancers and cell lines.
Protein type: Protein kinase, CAMK; Protein kinase, Ser/Thr (non-receptor); Kinase, protein; Tumor suppressor; EC 2.7.11.1; CAMK group; RAD53 family
Chromosomal Location of Human Ortholog: 22q12.1
Cellular Component: nucleoplasm; Golgi apparatus; PML body; chromosome, telomeric region
Molecular Function: identical protein binding; protein serine/threonine kinase activity; protein binding; protein homodimerization activity; metal ion binding; ubiquitin protein ligase binding; protein kinase binding; ATP binding
Biological Process: DNA damage induced protein phosphorylation; transcription, DNA-dependent; protein stabilization; positive regulation of transcription, DNA-dependent; protein amino acid autophosphorylation; DNA damage response, signal transduction; protein amino acid phosphorylation; regulation of transcription, DNA-dependent; DNA damage response, signal transduction resulting in induction of apoptosis; cell division; cellular protein catabolic process; double-strand break repair; DNA damage checkpoint; response to gamma radiation; regulation of protein catabolic process; G2/M transition of mitotic cell cycle; response to DNA damage stimulus
Disease: Li-fraumeni Syndrome 2; Breast Cancer; Prostate Cancer; Osteogenic Sarcoma
Research Articles on CHEK2
1. selective targeting of Chk1 and Chk2 by oncolytic adenovirus mutants was chosen to treat resistant tumor xenograft mice, and the maximum antitumoral efficacy was achieved with the combined co-abrogation of Chk1 and Chk2
Precautions
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Disclaimer
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