C2orf24 antibody

Catalog No. ABIN1387180

Product Details anti-C2orf24 Antibody

Target: C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C2orf24 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 C2orf24

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 C2orf24

Target: C2orf24 (Chromosome 2 Open Reading Frame 24 (C2orf24))

Alternative Name: C2orf24 (C2orf24 Products)

Synonyms: c2orf24 antibody, wu:fa05h07 antibody, zgc:55857 antibody, MGC75999 antibody, C12H2orf24 antibody, MGC115028 antibody, DKFZp459J1014 antibody, C2orf24 antibody, CGI-57 antibody, C2H2orf24 antibody, C7H2orf24 antibody, 1810031K17Rik antibody, AU043960 antibody, RGD735175 antibody, cyclin Pas1/PHO80 domain containing 1 antibody, cyclin Pas1/PHO80 domain containing 1 L homeolog antibody, cnppd1 antibody, CNPPD1 antibody, cnppd1.L antibody, Cnppd1 antibody

Background:

Synonyms: CDABP0125, CGI 57, chromosome 2 open reading frame 24, CNPD1_HUMAN, CNPPD1, Cyclin Pas1/PHO80 domain-containing protein 1, Protein CNPPD1.

Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf24 gene product has been provisionally designated C2orf24 pending further characterization.

Gene ID: 27013