C4orf14 antibody (Cy7)

Catalog No. ABIN1423694

The Rabbit Polyclonal anti-C4orf14 antibody has been validated for WB and IF (p). It is suitable to detect C4orf14 in samples from Human, Mouse and Rat.

Quick Overview for C4orf14 antibody (Cy7) (ABIN1423694)

Target: C4orf14 (Chromosome 4 Open Reading Frame 14 (C4orf14))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C4orf14 antibody is conjugated to Cy7

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

Product Details anti-C4orf14 Antibody (Cy7)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C4orf14

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 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 C4orf14

Target: C4orf14 (Chromosome 4 Open Reading Frame 14 (C4orf14))

Alternative Name: C4orf14

Background:

Synonyms: mAtNOS1, Chromosome 4 open reading frame 14, hAtNOS1, Hypothetical protein LOC84273, MGC3232, Putative ortholog of Arabidopsis mitochondrial nitric oxide synthase, Uncharacterized protein C4orf14, NOA1_HUMAN.

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 C4orf14 gene product has been provisionally designated C4orf14 pending further characterization.

Gene ID: 84273