ANKS3 antibody (PE)

Catalog No. ABIN1434432

The PE-conjugated Rabbit Polyclonal anti-ANKS3 antibody (ABIN1434432) specifically detects ANKS3 in IF (p). The antibody is reactive with Human, Mouse, Rat, Cow and Dog samples.

Quick Overview for ANKS3 antibody (PE) (ABIN1434432)

Target: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Reactivity: Human, Mouse, Rat, Cow, Dog

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ANKS3 antibody is conjugated to PE

Application: Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-ANKS3 Antibody (PE)

Cross-Reactivity: Rat (Rattus), Dog (Canine), Cow (Bovine)

Purification: purified by Protein A

Immunogen: KLH conjugated synthetic peptide derived from human ANKS3

Isotype: IgG

Application Details

Comment:

Excitation / Emission wavelength: 496nm / 578nm

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 µg/µL

Buffer: Aqueous buffered solution containing 100 µg/mL BSA, 50 % glycerol and 0.09 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C

Storage Comment: Store at 4 °C for 12 months

Expiry Date: 12 months

Target Details for ANKS3

Target: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Alternative Name: ANKS3

Background: ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Gene ID: 124401

HGNC: 0