FAM217B antibody (AA 1-82) (AbBy Fluor® 350)

Catalog No. ABIN1692625

This Rabbit Polyclonal antibody specifically detects FAM217B in WB, IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for FAM217B antibody (AA 1-82) (AbBy Fluor® 350) (ABIN1692625)

Target: FAM217B (Family with Sequence Similarity 217, Member B (FAM217B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM217B antibody is conjugated to AbBy Fluor® 350

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

Product Details anti-FAM217B Antibody (AbBy Fluor® 350)

Binding Specificity: AA 1-82

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf177

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 FAM217B

Target: FAM217B (Family with Sequence Similarity 217, Member B (FAM217B))

Alternative Name: C20orf177

Background:

Synonyms: C20orf177, CT177_HUMAN, dJ551D2.5, Uncharacterized protein C20orf177.

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf177 gene product has been provisionally designated C20orf177 pending further characterization.