DGCR14 antibody (AA 217-244)

Catalog No. ABIN657859

Product Details anti-DGCR14 Antibody

Target: DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))

Binding Specificity: AA 217-244

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DGCR14 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This DGCR14 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 217-244 amino acids from the Central region of human DGCR14.

Clone: RB21365

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

Storage Comment: DGCR14 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Expiry Date: 6 months

Target Details for DGCR14

Target: DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))

Alternative Name: DGCR14 (DGCR14 Products)

Synonyms: DGCR13 antibody, DGS-H antibody, DGS-I antibody, DGSH antibody, DGSI antibody, ES2 antibody, Es2el antibody, AI462402 antibody, D16H22S1269E antibody, Dgcr1 antibody, Dgsi antibody, fc19d10 antibody, wu:fc19d10 antibody, zgc:162979 antibody, MGC82189 antibody, DGCR14 antibody, es2 antibody, dgsi antibody, dgs-h antibody, dgs-i antibody, es2el antibody, dgcr13 antibody, ess-2 splicing factor homolog antibody, DiGeorge syndrome critical region gene 14 antibody, ess-2 splicing factor homolog S homeolog antibody, ESS2 antibody, Dgcr14 antibody, ess2 antibody, Ess2 antibody, DGCR14 antibody, ess2.S antibody

Background: This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus.

Molecular Weight: 52568

Gene ID: 8220

NCBI Accession: NP_073210

UniProt: Q96DF8