Glypican 3 (GPC3) (C-term) Rabbit Polyclonal Antibody
Other products for "GPC3"
Specifications
Product Data | |
Applications | WB |
Recommended Dilution | ELISA: 1/1000. Western Blot: 1/100 - 1/500. |
Reactivities | Human |
Host | Rabbit |
Isotype | Ig |
Clonality | Polyclonal |
Immunogen | KLH conjugated synthetic peptide between 464-494 amino acids from the C-terminal region of human GPC3 |
Specificity | This antibody reacts to GPC3. |
Formulation | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column; followed by peptide affinity purification. State: Aff - Purified State: Liquid purified Ig fraction |
Concentration | lot specific |
Purification | Affinity chromatography on Protein A |
Storage | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. |
Stability | Shelf life: one year from despatch. |
Predicted Protein Size | 65563 Da |
Gene Name | Homo sapiens glypican 3 (GPC3), transcript variant 2 |
Database Link | |
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 | Intestinal protein OCI-5, GTR2-2, MXR7, OCI5 |
Reference Data | |
Protein Families | Druggable Genome |
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