C21orf58 antibody (HRP)

Catalog No. ABIN1423612

This Rabbit Polyclonal antibody specifically detects C21orf58 in WB and IHC (p). It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for C21orf58 antibody (HRP) (ABIN1423612)

Target: C21orf58 (Chromosome 21 Open Reading Frame 58 (C21orf58))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C21orf58 antibody is conjugated to HRP

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

Product Details anti-C21orf58 Antibody (HRP)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C21orf58

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, 0.03 % 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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 C21orf58

Target: C21orf58 (Chromosome 21 Open Reading Frame 58 (C21orf58))

Alternative Name: C21orf58

Background:

Synonyms: C21orf58, Chromosome 21 open reading frame 58, CU058_HUMAN, Hypothetical protein LOC54058, Uncharacterized protein C21orf58.

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 C21orf58 gene product has been provisionally designated C21orf58 pending further characterization.

Gene ID: 54058