C21orf59 antibody (AA 151-250) (Cy5)

Catalog No. ABIN1705095

This anti-C21orf59 antibody is a Rabbit Polyclonal antibody detecting C21orf59 in WB, IF (cc) and IF (p). Suitable for Human.

Quick Overview for C21orf59 antibody (AA 151-250) (Cy5) (ABIN1705095)

Target: C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C21orf59 antibody is conjugated to Cy5

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-C21orf59 Antibody (Cy5)

Binding Specificity: AA 151-250

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C21orf59

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for C21orf59

Target: C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))

Alternative Name: C21orf59

Background:

Synonyms: C21orf48, C21orf59, Chromosome 21 open reading frame 59, CU059_HUMAN, FLJ20467, FLJ37137, FLJ40247, Uncharacterized protein C21orf59.

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. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.

Gene ID: 56683