RBBP8NL antibody (AA 21-120) (FITC)

Catalog No. ABIN1709997

This anti-RBBP8NL antibody is a Rabbit Polyclonal antibody detecting RBBP8NL in WB, IF (cc) and IF (p). Suitable for Human.

Quick Overview for RBBP8NL antibody (AA 21-120) (FITC) (ABIN1709997)

Target: RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RBBP8NL antibody is conjugated to FITC

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

Product Details anti-RBBP8NL Antibody (FITC)

Binding Specificity: AA 21-120

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C20orf151

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 RBBP8NL

Target: RBBP8NL (RBBP8 N-Terminal Like (RBBP8NL))

Alternative Name: C20orf151

Background:

Synonyms: C20orf151, Chromosome 20 open reading frame 151, CT151_HUMAN, RP5-908M14.6, Uncharacterized protein C20orf151.

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 C20orf151 gene product has been provisionally designated C20orf151 pending further characterization.

Gene ID: 140893