FAM207A antibody (AA 95-120)

Catalog No. ABIN1385685

Product Details anti-FAM207A Antibody

Target: FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))

Binding Specificity: AA 95-120

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM207A antibody is un-conjugated

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

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C21orf70

Isotype: IgG

Application Details

Application Notes: 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 FAM207A

Target: FAM207A (Family with Sequence Similarity 207, Member A (FAM207A))

Alternative Name: C21orf70 (FAM207A Products)

Synonyms: C21orf70 antibody, 1810008A18Rik antibody, AI303072 antibody, family with sequence similarity 207 member A antibody, family with sequence similarity 207, member A antibody, FAM207A antibody, Fam207a antibody

Background:

Synonyms: Chromosome 21 open reading frame 70, CU070_HUMAN, Hypothetical protein LOC85395, PRED56, Uncharacterized protein C21orf70.

Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.

Gene ID: 85395

UniProt: Q9NSI2