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ProductsBack/p57 Kip2 antibody

WB analysis of 293 cell lysate using GTX31859 p57 Kip2 antibody. Working concentration : (A) 1 and (B) 2 microg/ml

WB analysis of 293 cell lysate using GTX31859 p57 Kip2 antibody. Working concentration : (A) 1 and (B) 2 microg/ml

WB analysis of 293 cell lysate using GTX31859 p57 Kip2 antibody. Working concentration : (A) 1 and (B) 2 microg/ml

p57 Kip2 antibody

GTX31859

ApplicationsImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry

Product group Antibodies

TargetCDKN1C

Overview

Supplier
GeneTex
Product Name
p57 Kip2 antibody
Delivery Days Customer
9
Application Supplier Note
WB: 1 - 2 microg/mL. ICC/IF: 20 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
Applications
ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry
Certification
Research Use Only
Clonality
Polyclonal
Concentration
1 mg/ml
Conjugate
Unconjugated
Gene ID1028
Target name
CDKN1C
Target description
cyclin dependent kinase inhibitor 1C
Target synonyms
BWCR, BWS, KIP2, WBS, p57, p57Kip2, cyclin-dependent kinase inhibitor 1C, cyclin-dependent kinase inhibitor 1C (p57, Kip2), cyclin-dependent kinase inhibitor p57
Host
Rabbit
Isotype
IgG
Protein IDP49918
Protein Name
Cyclin-dependent kinase inhibitor 1C
Scientific Description
This gene is imprinted, with preferential expression of the maternal allele. The encoded protein is a tight-binding, strong inhibitor of several G1 cyclin/Cdk complexes and a negative regulator of cell proliferation. Mutations in this gene are implicated in sporadic cancers and Beckwith-Wiedemann syndorome, suggesting that this gene is a tumor suppressor candidate. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]
Storage Instruction
-20°C or -80°C,2°C to 8°C
UNSPSC
12352203

References

Effect of Butyrate on Collagen Expression, Cell Viability, Cell Cycle Progression and Related Proteins Expression of MG-63 Osteoblastic Cells. Chang MC et al., 2016, PLoS One
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