Western Blot: GPIHBP1 Antibody [NB110-41537] - (1) Detection of GPIHBP1in transfected lysate and (2) empty vector lysate was used as a negative control.
Immunocytochemistry/ Immunofluorescence: GPIHBP1 Antibody [NB110-41537] - GPIHBP1 antibody was tested in A431 cells with FITC (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and DyLight 550 (red).
Immunohistochemistry-Paraffin: GPIHBP1 Antibody [NB110-41537] - Analysis of FFPE mouse skeletal muscle using GPIHBP1 antibody at 1:50 on a Bond Rx autostainer (Leica Biosystems). The assay involved 20 minutes of heat ...read more
Use in Immunohistochemistry-Paraffin reported in scientific literature (PMID: 24735886). Use in chromatin immunoprecipitation reported in scientific literature (PMID: 28099936). Use in FLOW cell surface reported in scientific literature (PMID: 24735886).
Rat and Bovine reactivity reported in scientific literature (PMID: 24735886). Human reactivity reported in scientific literature (PMID: 28099936).
Packaging, Storage & Formulations
Storage
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
Tris-Glycine and 0.15M NaCl
Preservative
0.05% Sodium Azide
Concentration
0.6 mg/ml
Purity
Immunogen affinity purified
Alternate Names for GPIHBP1 Antibody
glycosylphosphatidylinositol anchored high density lipoprotein binding protein1
glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein1
GPI anchored high density lipoprotein binding protein 1
GPI-Anchored HDL-Binding Protein 1
GPIHBP1
GPI-HBP1
GPI-HBP1LOC338328
HBP1
High density lipoprotein-binding protein 1
HYPL1D
Background
GPIHBP1 (glycosylphosphatidylinositol-anchored HDL-binding protein 1) is a glycosylphosphatidylinositol-anchored glycoprotein of capillary endothelial cells that shuttle lipoprotein lipase (LPL) from the interstitial spaces to capillary lumen, and is essential for triglyceride-rich lipoproteins metabolism in mammalian plasma. GPIHBP1 is localized on luminal/abluminal capillary endothelial cell surfaces where it is bound by a glycosylphosphatidylinositol anchor and associates strongly with LPL. It serves as LPL transporter from sub-endothelial spaces to luminal face of capillaries, enabling lipolysis of circulating triglycerides localized within plasma chylomicrons. It has high affinity for HDL and binds to LPL, chylomicrons as well as APOA5. In the absence of GPIHBP1, the stores of catalytically active LPL within tissues are normal, but the LPL is mislocalized to interstitial spaces and is absent from capillary lumen. LPL mislocalization interferes with lipoprotein lipolysis and causes chylomicronemia. In humans, loss of function GPIHBP1 mutations leads to familial chylomicronemia. It binds LPL and apoA-V strongly for serving as a platform for lipolysis within capillaries, particularly in tissues which show high expression levels for both GPIHBP1 and LPL genes, such as heart, skeletal muscle and adipose tissue. Gpihbp1-/Gpihbp1- knock out mice have shown that GPIHBP1-deficiency causes severe hypertriglyceridemia.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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