Recombinant Human Glypican 3 Fc Chimera Avi-tag Protein, CF Summary
Details of Functionality |
Measured by its binding ability in a functional ELISA. Biotinylated Recombinant Human Glypican
3 Fc Chimera Avi-tag (Catalog # AVI11078) binds to Recombinant Human FGF
basic/FGF2/bFGF (Catalog #
233-FB/CF) with an ED 50 of 60.0-720 ng/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human Glypican 3 protein Human Glypican-3 (Gln25-His559) Accession # P51654.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | Avi-tag | N-terminus | | | C-terminus | |
|
N-terminal Sequence |
Gln25 |
Structure / Form |
Disulfide linked homodimer Biotinylated via Avi-tag |
Protein/Peptide Type |
Recombinant Proteins |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
89 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
>190 kDa, under non-reducing conditions. |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 3 months, -20 to -70 °C under sterile conditions after reconstitution.
|
Buffer |
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. |
Reconstitution Instructions |
Reconstitute at 250 μg/mL in water. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Glypican 3 Fc Chimera Avi-tag Protein, CF
Background
Glypican 3 (GPC3), also known as OCI5 and
MXR7, is a member of the heparan sulfate proteoglycan (HSPG) family (1).
In mammals, six glypican family members have been identified, all sharing
a structurally common extracellular domain (ECD) with a large globular cysteine-rich domain (CRD) with 14 invariant
cysteine residues, a stalk-like region containing the heparan sulfate
attachment sites, and a C‑terminal GPI attachment site. The ECD of GPC3 can be cleaved by furin to produce two
subunits that are linked by disulfide bonds: a 40 kDa N‑terminal alpha subunit
that can be secreted into the blood and a 30 kDa membrane-bound C‑terminal beta
subunit containing two HS glycan chains (1-3). Within ECD, human GPC3 shares
96% amino acid sequence identity with both mouse and rat GPC3. Several isoforms
of GPC3 due to alternative splicing have been reported (1). GPC3 is widely
expressed on the membrane of various embryonic cells, but not on those in adult
liver, and is involved in the regulation of growth and development of the body
(4). GPC3 is over-expressed in hepatocellular carcinomas and binding of GPC3 to
CD81 promotes development of carcinomas by activation of Hippo pathways in
hepatocytes (5). GPC3 is an important biomarker present in the serum of
hepatocellular carcinoma patients, which distinguishes benign from cancerous
nodules (6). Loss-of-function mutations in GPC3 are associated with Simpson-Golabi-Behmel
(SGB) syndrome, a condition characterized by tissue overgrowth
(dysmorphogenesis) (7). Our Avi-tag Biotinylated Recombinant Glypican 3 features biotinylation at a single site contained within the Avi-tag, a unique 15 amino acid peptide. Protein orientation will be uniform when bound to streptavidin-coated surface due to the precise control of biotinylation and the rest of the protein is unchanged so there is no interference in the protein's bioactivity.
- Ho, M. and Kim, H. (2012) Eur. J. Cancer. 47:333.
- Haruyama, Y. and Kataoka, H. (2016) World J. Gastroenterol. 22:275.
- Shimizu, Y. et al. (2019) Front Oncol. 9:248.
- Gonzales, A.D. et al. (1998) J. Cell Biol. 141:1407.
- Xue, Y. et al. (2018) Am J Pathol. 188(6):1469.
- Ge, S. et al. (2018) Filmus, Int J Clin Exp Pathol. 11(12):5774.
- Pilia, G. et al. (1996) Nature Genet.12:241.
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