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>   首页   >   产品   >   一抗   >   精选抗体   >   磷酸化抗体   >   phospho-COP1 (Ser387) Rabbit pAb   

phospho-COP1 (Ser387) Rabbit pAb

     
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
IHC-P, IHC-F, IF
Primary Accession Q8NHY2
Other Accession Q8NHY2
Host Rabbit
Clonality Polyclonal
Calculated MW 80474 Da
Physical State Liquid
Immunogen KLH conjugated synthesised phosphopeptide derived from human COP1 around the phosphorylation site of Ser387
Epitope Specificity TA(p-S)QL
Isotype IgG
Purity affinity purified by Protein A
Buffer 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
SIMILARITY Belongs to the COP1 family. Contains 1 RING-type zinc finger. Contains 7 WD repeats.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Background Descriptions COP1 is an E3 ubiquitin ligase protein that mediates ubiquitination and degradation of target proteins such as c-Jun and p53. It is a component of the DCX DET1-COP1 ubiquitin ligase complex which consists of RBX1, DET1, DDB1, CUL4A and COP1. Localizing to the cytoplasm and to the nucleus, COP1 is primarily expressed in testis, placenta, heart and skeletal muscle. COP1 is a potent inhibitor of p53-dependent transcription and apoptosis but, when phosphorylated by Atm (ataxia telangiectasia mutated) in response to DNA damage, the COP1-p53 complex is disrupted and p53 is allowed to exert its pro-apoptotic properties. In ovarian and breast cancers, COP1 is overexpressed, suggesting a role for COP1 in tumorigenesis.
Additional Information
Gene ID 64326
Other Names CFAP78; FAP78; RFWD2; RNF200; COP1_HUMAN; COP1; Constitutive photomorphogenesis protein 1 homolog (hCOP1); RING finger and WD repeat domain protein 2; RING finger protein 200; RING-type E3 ubiquitin transferase RFWD2; 2.3.2.27; COP1_MOUSE; Constitutive photomorphogenesis protein 1 homolog (mCOP1); COP1 E3 ubiquitin ligase; ring finger and WD repeat domain 2; constitutive photomorphogenic protein 1 (Arabidopsis); COP1 (phospho-S387); p-COP1; phospho-COP1; COP1 (phospho-Ser387)
Dilution IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
StorageStore at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name COP1 (HGNC:17440)
Function E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent proteasomal degradation of target proteins. E3 ubiquitin ligases accept ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Involved in JUN ubiquitination and degradation. Directly involved in p53 (TP53) ubiquitination and degradation, thereby abolishing p53-dependent transcription and apoptosis. Ubiquitinates p53 independently of MDM2 or RCHY1. Probably mediates E3 ubiquitin ligase activity by functioning as the essential RING domain subunit of larger E3 complexes. In contrast, it does not constitute the catalytic RING subunit in the DCX DET1-COP1 complex that negatively regulates JUN, the ubiquitin ligase activity being mediated by RBX1. Involved in 14-3-3 protein sigma/SFN ubiquitination and proteasomal degradation, leading to AKT activation and promotion of cell survival. Ubiquitinates MTA1 leading to its proteasomal degradation. Upon binding to TRIB1, ubiquitinates CEBPA, which lacks a canonical COP1-binding motif (Probable).
Cellular Location Nucleus speckle. Cytoplasm. Note=In the nucleus, it forms nuclear speckles
Tissue Location Ubiquitously expressed at low level. Expressed at higher level in testis, placenta, skeletal muscle and heart
Research Areas
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