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COPS3/CSN3 Monoclonal Antibody

Applications

  • WB
  • FCM
  • IHC-P
  • IF(ICC)
  • IHC

Reactivity

  • Human
  • Mouse
  • Rat
Overview
Catalog # bsm-54654R
Product Name COPS3/CSN3 Monoclonal Antibody
Applications WB, FCM, IHC-P, IF(ICC), IHC
Reactivity Human, Mouse, Rat
Specifications
Conjugation Unconjugated
Host Rabbit
Source Synthetic Peptide within C terminal human COPS3/CSN3.
Clonality Monoclonal
Clone # 1F8
Isotype IgG
Concentration 1ug/ul
Purification Purified by Protein A.
Storage Buffer Aqueous buffered solution containing 1xTBS (pH7.4), 1%BSA, 40%Glycerol and 0.05% Sodium Azide.
Storage Condition Store at -20°C for 12 months.
Target
Gene ID 8533
Swiss Prot Q9UNS2
Subcellular location Cytoplasm, Nucleus
Synonyms Constitutive photomorphogenic homolog subunit 3 antibody, COP 9 (constitutive photomorphogenic) subunit 3 antibody, COP 9 complex homolog subunit 3 antibody, COP 9 complex S3 antibody, COP 9 complex subunit 3 antibody, COP 9 constitutive photomorphogenic homolog subunit 3 antibody, COP 9 homolog antibody, COP 9 signalosome complex subunit 3 antibody, COP 9 signalosome subunit 3 antibody, COP 9 subunit 3 antibody, COP9 (constitutive photomorphogenic) subunit 3 antibody, COP9 complex homolog subunit 3 antibody, COP9 complex S3 antibody, COP9 complex subunit 3 antibody, COP9 constitutive photomorphogenic homolog subunit 3 antibody, COP9 homolog antibody, COP9 signalosome complex subunit 3 antibody, COP9 signalosome subunit 3 antibody, COP9 subunit 3 antibody, COPS 3 antibody, cops3 antibody, CSN 3 antibody, CSN3 antibody, CSN3_HUMAN antibody, JAB 1 containing signalosome subunit 3 antibody, JAB1 containing signalosome subunit 3 antibody, JAB1-containing signalosome subunit 3 antibody, SGN 3 antibody, SGN3 antibody, Signalosome subunit 3 antibody
Background The protein encoded by this gene possesses kinase activity that phosphorylates regulators involved in signal transduction. It phosphorylates I kappa-Balpha, p105, and c-Jun. It acts as a docking site for complex-mediated phosphorylation. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010].
Application Dilution
WB 1:300-5000
FCM 1:20-100
IHC-P 1:200-400
IF(ICC) 1:50-200
IHC