C9orf169 antibody (AA 1-100) (Cy3)

Catalog No. ABIN1701759

This anti-C9orf169 antibody is a Rabbit Polyclonal antibody detecting C9orf169 in WB, IF (cc) and IF (p). Suitable for Human.

Quick Overview for C9orf169 antibody (AA 1-100) (Cy3) (ABIN1701759)

Target: C9orf169 (C9ORF169) (Chromosome 9 Open Reading Frame 169 (C9ORF169))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C9orf169 antibody is conjugated to Cy3

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

Product Details anti-C9orf169 Antibody (Cy3)

Binding Specificity: AA 1-100

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf169

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 C9orf169

Target: C9orf169 (C9ORF169) (Chromosome 9 Open Reading Frame 169 (C9ORF169))

Alternative Name: C9orf169

Background:

Synonyms: C9orf169, Chromosome 9 open reading frame 169, CI169_HUMAN, MGC59937, UPF0574 protein C9orf169.

Background: C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought 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.

Gene ID: 375791