CCZ1 antibody

Catalog No. ABIN1388031

This anti-CCZ1 antibody is a Rabbit Polyclonal antibody detecting CCZ1 in WB, IF (p) and IHC (p). Suitable for Human, Mouse and Rat.

Quick Overview for CCZ1 antibody (ABIN1388031)

Target: CCZ1 (CCZ1 Vacuolar Protein Trafficking and Biogenesis Associated Homolog (S. Cerevisiae) (CCZ1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCZ1 antibody is un-conjugated

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

Product Details anti-CCZ1 Antibody

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCZ1

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 CCZ1

Target: CCZ1 (CCZ1 Vacuolar Protein Trafficking and Biogenesis Associated Homolog (S. Cerevisiae) (CCZ1))

Alternative Name: CCZ1

Background:

Synonyms: C7orf28A, CCZ1 vacuolar protein trafficking and biogenesis associated homolog S. cerevisiae, CCZ1A, CGI-43, H_DJ1163J12.2, Vacuolar fusion protein CCZ1 homolog, CCZ1_HUMAN.

Background: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf28 gene product has been provisionally designated C7orf28 pending further characterization.