FAM107B antibody

Catalog No. ABIN7247411

Product Details anti-FAM107B Antibody

Target: FAM107B (Family with Sequence Similarity 107, Member B (FAM107B))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM107B antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC)

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Fusion protein of human FAM107B

Isotype: IgG

Application Details

Application Notes: IHC 1:150-1:300, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.32 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for FAM107B

Target: FAM107B (Family with Sequence Similarity 107, Member B (FAM107B))

Alternative Name: FAM107B (FAM107B Products)

Synonyms: C10orf45 antibody, 3110001A13Rik antibody, AA589595 antibody, AA959793 antibody, AI132312 antibody, family with sequence similarity 107 member B antibody, family with sequence similarity 107, member B antibody, FAM107B antibody, Fam107b antibody

Background: FAM107B is a 131 amino acid protein that is encoded by a gene that maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.

UniProt: Q9H098