COPS3/CSN3 Monoclonal Antibody
Applications
Reactivity
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 |