C4orf40 antibody (AA 21-120) (FITC)

Catalog No. ABIN1709122

This Rabbit Polyclonal antibody specifically detects C4orf40 in IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for C4orf40 antibody (AA 21-120) (FITC) (ABIN1709122)

Target: C4orf40 (C4ORF40) (Chromosome 4 Open Reading Frame 40 (C4ORF40))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C4orf40 antibody is conjugated to FITC

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

Product Details anti-C4orf40 Antibody (FITC)

Binding Specificity: AA 21-120

Purpose: C4orf40 Polyclonal Antibody, FITC Conjugated

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C4orf40

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, 0.02 % 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: -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 C4orf40

Target: C4orf40 (C4ORF40) (Chromosome 4 Open Reading Frame 40 (C4ORF40))

Alternative Name: C4orf40

Background:

Synonyms: C4orf40, CD040_HUMAN, Uncharacterized protein C4orf40.

Background: Representing approximately 6 % of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf40 gene product has been provisionally designated C4orf40 pending further characterization.