CACFD1 antibody (AA 41-130)

Catalog No. ABIN1714608

The Rabbit Polyclonal anti-CACFD1 antibody (ABIN1714608) specifically detects CACFD1 in WB, IF (cc), IF (p), IHC (fro) and IHC (p). The antibody is reactive with Human samples.

Quick Overview for CACFD1 antibody (AA 41-130) (ABIN1714608)

Target: CACFD1 (Calcium Channel Flower Domain Containing 1 (CACFD1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CACFD1 antibody is un-conjugated

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

Product Details anti-CACFD1 Antibody

Binding Specificity: AA 41-130

Purpose: C9orf7 Polyclonal Antibody

Predicted Reactivity: Human,Mouse,Rat,Dog,Pig,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf7

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000),

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 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for CACFD1

Target: CACFD1 (Calcium Channel Flower Domain Containing 1 (CACFD1))

Alternative Name: C9orf7

Background:

Synonyms: C9orf7, Calcium channel flower homolog, Chromosome 9 open reading frame 7, D9S2135, FLOWR_HUMAN, RP13-100B2.5.

Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterization.

Gene ID: 11094