SKIDA1 antibody (Biotin)

Catalog No. ABIN1404601

This Rabbit Polyclonal antibody specifically detects SKIDA1 in WB and IHC (p). It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for SKIDA1 antibody (Biotin) (ABIN1404601)

Target: SKIDA1 (SKI/DACH Domain Containing 1 (SKIDA1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SKIDA1 antibody is conjugated to Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-SKIDA1 Antibody (Biotin)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C10orf140

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400

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 for 12 months.

Expiry Date: 12 months

Target Details for SKIDA1

Target: SKIDA1 (SKI/DACH Domain Containing 1 (SKIDA1))

Alternative Name: C10orf140

Background:

Synonyms: C10orf140, chromosome 10 open reading frame 140, DKFZp761J229, DLN 1, DLN1_HUMAN, FLJ45187, Protein DLN-1.

Background: C10orf140, also known as DLN-1, is an 827 amino acid protein that belongs to the DACH/dachshund family. C10orf140 contains a poly-Alanine region that is highly polymorphic. The gene encoding C10orf140 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Gene ID: 387640