GPC3 polyclonal, anti-human, mouse
€295.00
In stock
SKU
K003093P
Catalog Number: K003093P
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB, IHC
Request Manual
Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB, IHC
Request Manual
Questions? Contact us!
Background:
Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants.
Synonyms: DGSX, GTR2-2, MXR7, OCI-5, SDYS, SGB, SGBS, SGBS1
Cellular Location: Cell membrane Extracellular side GPI-anchor Lipid-anchor Secreted extracellular space
Immunogen:
Recombinant protein of human GPC3
Gene Symbol: GPC3
Gene ID: 2719
Swiss prot: P51654
Calculated MW: 66kDa
Recommended dilution:
WB 1:500-2000, IHC 1:50-200,
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants.
Synonyms: DGSX, GTR2-2, MXR7, OCI-5, SDYS, SGB, SGBS, SGBS1
Cellular Location: Cell membrane Extracellular side GPI-anchor Lipid-anchor Secreted extracellular space
Immunogen:
Recombinant protein of human GPC3
Gene Symbol: GPC3
Gene ID: 2719
Swiss prot: P51654
Calculated MW: 66kDa
Recommended dilution:
WB 1:500-2000, IHC 1:50-200,
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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