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Antibodies

Recombinant Glypican 3 Monoclonal Antibody

Product Sizes
50 ul
£281.00
AN301534L-50UL
100 ul
£402.00
AN301534L-100UL
About this Product
SKU:
AN301534L
Additional Names:
MXR;GPC;UNQ;PRO;CDw;ADAM;Protein FOAP;Secreted glypican;Glypican proteoglycan;Sialic acid-binding Ig-like lectin;C20orf;OCI;GPC3;DGSX;GTR2-2;MXR7;OCI-5;SDYS;SGB;SGBS;SGBS1;glypican-3;CDw329;Glypican 3;Glypican proteoglycan 3;Glypican-3 [Precursor];GTR2 2;Heparan sulphate proteoglycan;Intestinal protein OCI 5;Intestinal protein OCI-5;OCI 5;Protein FOAP-9;Secreted glypican-3;Sialic acid-binding Ig-like lectin 9;SIGLEC9;Siglec-9;ADAM33;C20orf153;UNQ873;PRO1891;OCI5
Application:
Flow Cytometry, Immunofluorescence, Immunoprecipitation, Western Blot
Buffer:
PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
translate.label.attr.clone:
A233
Clonality:
Recombinant Monoclonal
Concentration:
1 mg/ml
Extra Details:
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.
Host:
Rabbit
Immunogen:
Recombinant human Glypican 3 fragment
Isotype:
IgG, kappa
Purification:
Protein A Purified
Reactivities:
Human
Shipping Conditions:
Blue Ice
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Elabscience
Type:
Antibody: Recombinant Antibodies