ZSWIM3 antibody (Cy7)

Catalog No. ABIN1418924

The Rabbit Polyclonal anti-ZSWIM3 antibody is suitable to detect ZSWIM3 in samples from Human, Mouse and Rat. It has been validated for WB and IF (p).

Quick Overview for ZSWIM3 antibody (Cy7) (ABIN1418924)

Target: ZSWIM3 (Zinc Finger, SWIM-Type Containing 3 (ZSWIM3))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ZSWIM3 antibody is conjugated to Cy7

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

Product Details anti-ZSWIM3 Antibody (Cy7)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human ZSWIM3

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 ZSWIM3

Target: ZSWIM3 (Zinc Finger, SWIM-Type Containing 3 (ZSWIM3))

Alternative Name: ZSWIM3

Background:

Synonyms: Zinc finger SWIM domain containing protein 3, C20orf164, Zinc finger SWIM type containing 3, ZSWIM 3, ZSWM3_HUMAN.

Background: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZSWIM3 (Zinc finger SWIM domain-containing protein 3) is a 696 amino acid protein that contains one SWIM-type zinc finger. SWIM domains are found in a variety of eukaryotic and prokaryotic proteins and are thought to be critical for certain ubiquitination reactions. The gene encoding ZSWIM3 maps to human chromosome 20, which contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.

Gene ID: 140831