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.

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.

Mouse,Human,Rat,Cow,Horse

WB

WB 1:500-2000

53kD

64645

Q96MC6

https://www.uniprot.org/uniprotkb/Q96MC6

Membrane; Multi-pass membrane protein (Potential).

KLH conjugated synthetic peptide derived from human HIAT1

Rabbit

Polyclonal

affinity purified by Protein A

Liquid

0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.