CNTD2 antibody

Catalog No. ABIN1387142

The Rabbit Polyclonal anti-CNTD2 antibody has been validated for IF (p) and IHC (p). It is suitable to detect CNTD2 in samples from Human.

Quick Overview for CNTD2 antibody (ABIN1387142)

Target: CNTD2 (Cyclin N-terminal Domain Containing 2 (CNTD2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CNTD2 antibody is un-conjugated

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

Product Details anti-CNTD2 Antibody

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CNTD2

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 CNTD2

Target: CNTD2 (Cyclin N-terminal Domain Containing 2 (CNTD2))

Alternative Name: CNTD2

Background:

Synonyms: CNTD2, CNTD 2, CNTD-2, Cyclin N terminal domain containing 2, Cyclin N terminal domain containing protein 2, FLJ13265, CNTD2_HUMAN.

Background: CNTD2 (cyclin N-terminal domain containing 2) is a 155 amino acid protein that contains one cyclin N-terminal domain and is encoded by a gene that maps to human chromosome 19q13.2. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 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 killer cell and leukocyte Ig-like receptors, various ICAMs, the CEACAM and PSG families, 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 Bcl-3.

Gene ID: 79935