Recombinant Human Guanylyl Cyclase C Fc Avi-tag Protein, CF Summary
Additional Information |
Biotinylated |
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Human Guanylyl Cyclase C Antibody
(Catalog #
MAB2157) is immobilized at 100 ng/mL (100 µL/well), Biotinylated Recombinant Human Guanylyl Cyclase C Fc Chimera Avi-tag binds with an ED 50 of 0.500-3.00 ng/mL. Measured by its ability to inhibit neurite outgrowth of E16-E18 rat embryonic cortical neurons. 2.50 μg/mL of protein is able to significantly inhibit neurite outgrowth. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human Guanylyl Cyclase C/GUCY2C protein Human Guanylyl Cyclase C/GUCY2C (Ser24-Gln430) Accession # P25092.2 | IEGRMD | Human IgG1 (Pro100-Lys330) | Avi-tag | N-terminus | | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Ser24 |
Structure / Form |
Biotinylated via Avi-tag. |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Purity Statement |
Antigen Affinity-purified |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
74 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 |
105-120 kDa, under 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. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 1.00 mg/mL in PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Guanylyl Cyclase C Fc Avi-tag Protein, CF
Background
Guanylyl
Cyclase C (GUCY2C), also known as heat-stable enterotoxin receptor, is a
type I transmembrane protein of the guanylate cyclase (GC) family and
helps regulate intestinal function (1, 8). There are 7 known members of the GC
family (GC-A through GC-G) and they catalyze the conversion of guanosine
triphosphate to cyclic guanosine monophosphate (cGMP) and pyrophosphate (1-4).
Mature human GUCY2C consists of an extracellular domain (ECD) with a ligand
binding domain, a transmembrane segment and a cytoplasmic region possessing a pseudokinase
domain and a GC catalytic domain. The ECD of mature human GUCY2C shares 70% and
72% amino acid sequence identity with the ECD of mouse and rat GUCY2C,
respectively. GUCY2C is primarily expressed in intestinal epithelial cells from
the duodenum to rectum and binds to the endogenous gastrointestinal hormones
guanylin and uroguanylin (1-4). Activation of GUCY2C signaling mediates fluid-ion
homeostasis, intestinal inflammation, and cell proliferation in a
cGMP-dependent manner (5). GUCY2C is also expressed in neurons, where it plays
a role in attention deficiency/hyperactive behavior (6). GUCY2C is being
investigated as a treatment for several gastrointestinal disorders including irritable
bowel syndrome, obesity, colorectal cancer, and chronic idiopathic constipation
(7, 8). Our Avi-tag
Biotinylated GUCY2C
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.
- Arshad, N. and Visweswariah, S.S. (2012) FEBS Lett. 586:2835.
- Potter, L.R. (2011) Cell Signal. 2011 23:1921.
- Arshad, N. et al. (2013) J. Biol. Chem. 288:3907.
- Gibbons, A.V. et al. (2013) Cancer Res. 73:22.
- Lucas, K. et al. (2000) Pharmacol Rev. 52:375.
- Gong, R. et al. (2011) Science 333:1642.
- Waldman, S.A. and Camilleri, M. (2018) Gut 67:1543.
- Kim, G.W. et al. (2013) Trends Endocrinol Metab 24(4):165.
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