C21ORF56 antibody (Biotin)

Catalog No. ABIN1405717

This Rabbit Polyclonal antibody specifically detects C21ORF56 in WB and IHC (p). It exhibits reactivity toward Human.

Quick Overview for C21ORF56 antibody (Biotin) (ABIN1405717)

Target: C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C21ORF56 antibody is conjugated to Biotin

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

Product Details anti-C21ORF56 Antibody (Biotin)

Purpose: SPATC1L Polyclonal Antibody, Biotin Conjugated

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C21ORF56

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, 0.02 % 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: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for C21ORF56

Target: C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))

Alternative Name: C21ORF56

Background:

Synonyms: Chromosome 21 open reading frame 56, DKFZp434N0650, MGC99490, Uncharacterized protein C21orf56, SPC1L_HUMAN.

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 C21orf56 gene product has been provisionally designated C21orf56 pending further characterization.

Gene ID: 84221