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HIAT1 Rabbit pAb

HIAT1 Rabbit pAb

     
  • 1 - HIAT1 Rabbit pAb AP58843
    Sample: Placenta (Mouse) Lysate at 40 ug
    Primary: Anti-HIAT1 (AP58843)at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 53kD
    Observed band size: 50kD
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB
Primary Accession Q96MC6
Reactivity Mouse
Predicted Rat, Human, Horse
Host Rabbit
Clonality Polyclonal
Calculated MW 53027 Da
Physical State Liquid
Immunogen KLH conjugated synthetic peptide derived from human HIAT1
Epitope Specificity 1-50/490
Isotype IgG
Purity affinity purified by Protein A
Buffer 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
SUBCELLULAR LOCATION Membrane; Multi-pass membrane protein (Potential).
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Background Descriptions 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.
Additional Information
Gene ID 64645
Other Names Solute carrier family 71 member 1 {ECO:0000312|HGNC:HGNC:23363}, Hippocampus abundant transcript 1 protein {ECO:0000312|HGNC:HGNC:23363}, Major facilitator superfamily domain-containing 14A {ECO:0000312|HGNC:HGNC:23363}, Putative tetracycline transporter-like protein, SLC71A1 (HGNC:23363)
Dilution WB=1:500-2000
StorageStore at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name SLC71A1 (HGNC:23363)
Function Probable membrane-bound transporter. May play a role in neuronal nutrient sensing and energy homeostasis. Required for the final stages of spermatogenesis.
Cellular Location Membrane; Multi-pass membrane protein
Research Areas

BACKGROUND

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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