HIAT1 antibody (PE)

Catalog No. ABIN900692

The Rabbit Polyclonal anti-HIAT1 antibody has been validated for WB. It is suitable to detect HIAT1 in samples from Mouse, Human, Cow and Rat.

Quick Overview for HIAT1 antibody (PE) (ABIN900692)

Target: HIAT1 (Hippocampus Abundant Transcript 1 (HIAT1))

Reactivity: Mouse, Human, Cow, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HIAT1 antibody is conjugated to PE

Application: Western Blotting (WB)

Product Details anti-HIAT1 Antibody (PE)

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Cow,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HIAT1

Isotype: IgG

Application Details

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: Sodium azide

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

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 HIAT1

Target: HIAT1 (Hippocampus Abundant Transcript 1 (HIAT1))

Alternative Name: HIAT1

Background:

Synonyms: Hippocampus abundant gene transcript 1, Hippocampus abundant transcript, Hippocampus abundant transcript 1, Putative tetracycline transporter like protein, Tetracycline transporter like prot, MGC144858, rCG_28876, DKFZp564L0864, HIAT1_HUMAN.

Background: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.

Molecular Weight: 53kDa

Gene ID: 64645