ANGPTL4 FISH Probe

This gene encodes a glycosylated, secreted protein containing a C-terminal fibrinogen domain. The encoded protein is induced by peroxisome proliferation activators and functions as a serum hormone that regulates glucose homeostasis, lipid metabolism, and insulin sensitivity. This protein can also act as an apoptosis survival factor for vascular endothelial cells and can prevent metastasis by inhibiting vascular growth and tumor cell invasion. The C-terminal domain may be proteolytically-cleaved from the full-length secreted protein. Decreased expression of this gene has been associated with type 2 diabetes. Alternative splicing results in multiple transcript variants. This gene was previously referred to as ANGPTL2 but has been renamed ANGPTL4. [provided by RefSeq, Sep 2013]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
ANGPTL4-20-RE 20 (40 μL) 200 μL color Request Pricing
ANGPTL4-20-OR 20 (40 μL) 200 μL color Request Pricing
ANGPTL4-20-GO 20 (40 μL) 200 μL color Request Pricing
ANGPTL4-20-GR 20 (40 μL) 200 μL color Request Pricing
ANGPTL4-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

This gene encodes a glycosylated, secreted protein containing a C-terminal fibrinogen domain. The encoded protein is induced by peroxisome proliferation activators and functions as a serum hormone that regulates glucose homeostasis, lipid metabolism, and insulin sensitivity. This protein can also act as an apoptosis survival factor for vascular endothelial cells and can prevent metastasis by inhibiting vascular growth and tumor cell invasion. The C-terminal domain may be proteolytically-cleaved from the full-length secreted protein. Decreased expression of this gene has been associated with type 2 diabetes. Alternative splicing results in multiple transcript variants. This gene was previously referred to as ANGPTL2 but has been renamed ANGPTL4. [provided by RefSeq, Sep 2013]

Gene Details

Gene Symbol : ANGPTL4

Gene Name : Angiopoietin like 4

Chromosome : CHR 19: 836,412,6-837,437,4

Locus : 19p13.2

Alt. Genes : FEM1B

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