CCDC112 antibody (AA 301-400) (AbBy Fluor® 680)

Catalog No. ABIN5006601

This Rabbit Polyclonal antibody specifically detects CCDC112 in IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for CCDC112 antibody (AA 301-400) (AbBy Fluor® 680) (ABIN5006601)

Target: CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC112 antibody is conjugated to AbBy Fluor® 680

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-CCDC112 Antibody (AbBy Fluor® 680)

Binding Specificity: AA 301-400

Predicted Reactivity: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC112/MBC1

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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 CCDC112

Target: CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))

Alternative Name: MBC1

Background:

Synonyms: MBC1, Mutated in bladder cancer protein 1, coiled coil domain containing 112, coiled-coil domain containing 112, MBC1, CC112_HUMAN.

Background: CCDC112, also known as MBC1 (mutated in bladder cancer 1), is a 446 amino acid protein. The gene encoding CCDC112 is located on chromosome 5. Due to alternative splicing events, CCDC112 exists as two isoforms. Chromosome 5 comprises about 6 % of human genomic DNA and contains 181 million base pairs encoding around 1,000 genes. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome

Gene ID: 153733