C19orf54 antibody (Biotin)

Catalog No. ABIN1404073

This Rabbit Polyclonal antibody specifically detects C19orf54 in WB and IHC (p). It exhibits reactivity toward Human.

Quick Overview for C19orf54 antibody (Biotin) (ABIN1404073)

Target: C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C19orf54 antibody is conjugated to Biotin

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

Product Details anti-C19orf54 Antibody (Biotin)

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C19orf54

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.

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for C19orf54

Target: C19orf54 (Chromosome 19 Open Reading Frame 54 (C19orf54))

Alternative Name: C19orf54

Background:

Synonyms: Chromosome 19 open reading frame 54, FLJ17063, FLJ41131, Hypothetical protein LOC284325, MGC103014, UPF0692 protein C19orf54, CS054_HUMAN.

Background: C19orf54 is a 351 amino acid protein that exists as two alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

Gene ID: 284325