RBFA antibody

Catalog No. ABIN1385454

Product Details anti-RBFA Antibody

Target: RBFA (Ribosome Binding Factor A (RBFA))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RBFA antibody is un-conjugated

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human RBFA

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for RBFA

Target: RBFA (Ribosome Binding Factor A (RBFA))

Alternative Name: RBFA (RBFA Products)

Synonyms: C18orf22 antibody, HsT169 antibody, 1110032A13Rik antibody, AI595940 antibody, RGD1311910 antibody, zgc:162590 antibody, ribosome binding factor A antibody, RBFA antibody, Rbfa antibody, rbfa antibody

Background:

Synonyms: mitochondrial, C18orf25, Chromosome 18 open reading frame 22, HsT169, Hypothetical protein LOC79863, Putative ribosome binding factor A, mitochondrial precursor, Putative ribosome-binding factor A, rbfA, RBFA_HUMAN.

Background: C18orf22, also known as HsT169, is a 343 amino acid protein that localizes to the mitochondrion and is expressed as two alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.