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  • C0873 - Anti-CKS2 (36-50) antibody produced in rabbit

C0873 Sigma

Anti-CKS2 (36-50) antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution

Synonym: Anti-Cyclin-dependent kinases regulatory subunit 2, Anti-CKSHS2



Related Categories Alphabetical Index, Antibodies, CI-CN, Primary Antibodies
species reactivity   human
application(s)   western blot: 1:500-1:2,000
clone   polyclonal
antibody form   IgG fraction of antiserum
form   buffered aqueous solution
mol wt   antigen mol wt ~10 kDa
shipped in   dry ice
storage temp.   −20°C
Gene Information   human ... CKS2(1164)
biological source   rabbit
conjugate   unconjugated



synthetic peptide corresponding to amino acids 36-50 of human CKS2

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.


Anti-CKS2 (36-50) antibody produced in rabbit is suitable for western blotting at a working dilution of 1:500-1:2,000.

Yale Center for High Throughput Cell Biology IF-tested antibodies. Each antibody is tested by immunofluorescence against HUVEC cells using the Yale HTCB IF protocol. To learn more about the Sigma Life Science and Yale Center for High Throughput Cell Biology partnership, visit sigma.com/htcb-if.

Biochem/physiol Actions

Cyclin-dependent kinases regulatory subunit 2 is a protein encoded by the CKS2 gene in humans. It is a member of the human Cks family. It is also referred as CKSHS2. CKS2 protein helps in various biological functions by binding to the catalytic subunit of the cyclin dependent kinases and also helps in regulation of meiosis and mitosis. The CKS2 mRNA is found to be expressed in different phases of HeLa cells, cell cycle. Cks2 may act as an independent prognostic factor in patients with cholangiocarcinoma. It also plays an important role in the progression of cell cycle which causes cholangiocarcinoma and Bax-mediated mitochondrial caspase-dependent apoptosis. It may act as a biomarker for predicting superficial bladder cancer progression to muscle-invasive cancer and is a possible candidate for targeted molecular diagnosis and therapy in gastric cancer.

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Keywords: Amplification, Buffers, Cell biology, Enzyme-linked immunosorbent assay, Immunofluorescence, Immunohistochemistry, Immunoprecipitation, Molecular biology, Phosphorylations, Purification, Western blot

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