C4ORF29 antibody (AA 121-220) (Cy3)

Catalog No. ABIN1702037

The Rabbit Polyclonal anti-C4ORF29 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect C4ORF29 in samples from Mouse.

Quick Overview for C4ORF29 antibody (AA 121-220) (Cy3) (ABIN1702037)

Target: C4ORF29 (Chromosome 4 Open Reading Frame 29 (C4ORF29))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C4ORF29 antibody is conjugated to Cy3

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

Product Details anti-C4ORF29 Antibody (Cy3)

Binding Specificity: AA 121-220

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C4orf29

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 C4ORF29

Target: C4ORF29 (Chromosome 4 Open Reading Frame 29 (C4ORF29))

Alternative Name: C4orf29

Background:

Synonyms: C4orf29, CD029_HUMAN, Chromosome 4 open reading frame 29, Uncharacterized protein C4orf29.

Background: C4orf29 (chromosome 4 open reading frame 29) is a 414 amino acid secreted protein that exists as four alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human 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.

Gene ID: 80167