CCDC174 antibody (AA 1-100) (Biotin)

Catalog No. ABIN1700222

Product Details anti-CCDC174 Antibody (Biotin)

Target: CCDC174 (Coiled-Coil Domain Containing 174 (CCDC174))

Binding Specificity: AA 1-100

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC174 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Predicted Reactivity: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf19

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Expiry Date: 12 months

Target Details for CCDC174

Target: CCDC174 (Coiled-Coil Domain Containing 174 (CCDC174))

Alternative Name: C3orf19 (CCDC174 Products)

Synonyms: C3orf19 antibody, CCDC174 antibody, c3orf19 antibody, C130022K22Rik antibody, RGD1305225 antibody, coiled-coil domain containing 174 antibody, coiled-coil domain containing 174 S homeolog antibody, CCDC174 antibody, ccdc174.S antibody, Ccdc174 antibody

Background:

Synonyms: Ccdc174, Coiled coil domain containing 174, Uncharacterized protein C3orf19, CC174_HUMAN.

Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf19 gene product has been provisionally designated C3orf19 pending further characterization.