TRIM17 / RNF16 antibody (AbBy Fluor® 555)

Catalog No. ABIN1401185

The Rabbit Polyclonal anti-TRIM17 / RNF16 antibody has been validated for WB and IF (p). It is suitable to detect TRIM17 / RNF16 in samples from Human.

Quick Overview for TRIM17 / RNF16 antibody (AbBy Fluor® 555) (ABIN1401185)

Target: TRIM17 / RNF16 (TRIM17)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TRIM17 / RNF16 antibody is conjugated to AbBy Fluor® 555

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-TRIM17 / RNF16 Antibody (AbBy Fluor® 555)

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TRIM17/RNF16

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for TRIM17 / RNF16

Target: TRIM17 / RNF16 (TRIM17)

Alternative Name: RNF16

Background:

Synonyms: RBCC, RING finger protein 16, RNF16, TERF, Testis RING finger protein, TRIM 17, Tripartite mot protein 17, TRI17_HUMAN.

Background: The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Gene ID: 51127