CSN3 antibody (AA 325-375)

Catalog No. ABIN7449263

The Rabbit Polyclonal anti-CSN3 antibody has been validated for WB. It is suitable to detect CSN3 in samples from Human.

Quick Overview for CSN3 antibody (AA 325-375) (ABIN7449263)

Target: CSN3 (Casein kappa (CSN3))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CSN3 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-CSN3 Antibody

Binding Specificity: AA 325-375

Purpose: Rabbit anti-CSN3 Antibody, Affinity Purified

Predicted Reactivity: Mouse,Rat,Bovine,Orangutan

Purification: Affinity Purified

Immunogen: between AA 325 and 375

Isotype: IgG

Application Details

Application Notes: 1:2,000 - 1:20,000

Restrictions: For Research Use only

Handling

Concentration: 1000 μg/mL

Buffer: Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C

Expiry Date: 12 months

Target Details for CSN3

Target: CSN3 (Casein kappa (CSN3))

Alternative Name: CSN3

Background: Background: CSN3 is one of eight subunits (CSN1 to 8) of the highly conserved COP9 signalsome (CSN) complex originally identified as a regulator of light-mediated development in Arabidopsis. Characterization of CSN from yeast to mammals reveals its function as a modulator of signal transduction pathways involved in a variety of cellular and developmental processes. One of the major functions of the CSN is the regulation of protein degradation via intersection with the ubiquitin-proteasome pathway and regulation of E3-ubiquitin ligases. The CSN also possesses kinase activity. CSN3 is the kinase associated with the CSN complex that phosphorylates signal transducers such as I-kappa-Balpha, p105, and c-Jun. Human CSN3 maps to the Smith-Magenis syndrome locus. Microdeletions in this locus results in mental retardation, skeletal abnormalities, sleep disorder, and neurobehavior anomalies.

Gene ID: 8533

NCBI Accession: NP_003644

UniProt: Q9UNS2