FAM164A antibody (Biotin)

Catalog No. ABIN1403965

Product Details anti-FAM164A Antibody (Biotin)

Target: FAM164A (Family with Sequence Similarity 164, Member A (FAM164A))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM164A antibody is conjugated to Biotin

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C8orf70

Isotype: IgG

Application Details

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

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 FAM164A

Target: FAM164A (Family with Sequence Similarity 164, Member A (FAM164A))

Alternative Name: CGI62/C8orf70 (FAM164A Products)

Synonyms: fam164a antibody, fc28a05 antibody, wu:fc28a05 antibody, zgc:63810 antibody, DKFZp459P1730 antibody, C8orf70 antibody, FAM164A antibody, 3110050N22Rik antibody, AI790358 antibody, AU023959 antibody, Fam164a antibody, C14H8ORF70 antibody, RGD1311970 antibody, CGI-62 protein antibody, zinc finger, C2HC-type containing 1A antibody, zinc finger, C2HC-type containing 1A S homeolog antibody, zinc finger C2HC-type containing 1A antibody, Bm1_01920 antibody, zc2hc1a antibody, zc2hc1a.S antibody, ZC2HC1A antibody, Zc2hc1a antibody

Background:

Synonyms: C8orf70, Chromosome 8 open reading frame 70, F164A_HUMAN, fam164a, family with sequence similarity 164, member A, Hypothetical protein C8orf70, hypothetical protein LOC51101, Protein FAM164A, CGI 62, CGI-62.

Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf70 gene product has been provisionally designated C8orf70 pending further characterization.

Gene ID: 4879