GPIHBP1 Antilichaam

This gene encodes a capillary endothelial cell protein that facilitates the lipolytic processing of triglyceride-rich lipoproteins. The encoded protein is a glycosylphosphatidylinositol-anchored protein that is a member of the lymphocyte antigen 6 (Ly6) family. This protein plays a major role in transporting lipoprotein lipase (LPL) from the subendothelial spaces to the capillary lumen. Mutations in this gene are the cause of hyperlipoproteinemia, type 1D. Alternate splicing results in multiple transcript variants.

338328

Q8IV16

Human

Recombinant fusion protein containing a sequence corresponding to amino acids 50-151 of human GPIHBP1 (NP_835466.2) .

Unconjugated

Primary Antibodies

Signal Transduction

Affinity purification

U-87MG

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 20kDa

IgG

WB: 1:500 - 1:2000

GPIHBP1

LO2

Glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1

Homo sapiens

GPI-HBP1, HYPL1D, glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1, GPI anchored high density lipoprotein binding protein 1, GPI-anchored HDL-binding protein 1, endothelial cell LPL transporter

WB

Liquid