FAM203B antibody

Catalog No. ABIN7244606

The Rabbit Polyclonal anti-FAM203B antibody has been validated for ELISA and IHC. It is suitable to detect FAM203B in samples from Human.

Quick Overview for FAM203B antibody (ABIN7244606)

Target: FAM203B (Family with Sequence Similarity 203, Member B (FAM203B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM203B antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC)

Product Details anti-FAM203B Antibody

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Synthetic peptide of human HGH1

Isotype: IgG

Application Details

Application Notes: IHC 1:30-1:150, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.6 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 FAM203B

Target: FAM203B (Family with Sequence Similarity 203, Member B (FAM203B))

Alternative Name: HGH1

Background: HGH1, is also known as BRP16, Brp16 is a 256 amino acid protein encoded by a gene on human chromosome 8. 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.

UniProt: Q9BTY7