Recombinant Human VSTM2A Fc Chimera Avi-tag Protein, CF Summary
Additional Information |
Biotinylated |
Details of Functionality |
Measured by its ability to inhibit anti-CD3 antibody induced IL-2 or IFN-gamma secretion by human T cells. The ED 50 for this effect is 1.00-10.0 μg/mL Measured by its binding ability in a functional ELISA. When Human VSTM2A Antibody
(Catalog #
MAB100371) is immobilized at 0.5 µg/mL (100 µL/well), Biotinylated Recombinant Human VSTM2A Fc Chimera Avi-tag (Catalog # AV10704) binds with an ED 50 of 1.00-8.00 ng/mL. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human VSTM2A protein Human VSTM2A (Ser25-Phe244) Accession # NP_001304772.1 | IEGRMD | Human IgG1 (Pro100-Lys330) | Avi-tag | N-terminus | | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Ser25 |
Structure / Form |
Disulfide-linked homodimer, biotinylated via Avi-tag |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
53 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 |
62-75 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 |
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 500 μg/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 VSTM2A Fc Chimera Avi-tag Protein, CF
Background
V-set
and transmembrane domain-containing protein 2A (VSTM2A) is a secreted
glycoprotein that is a member of the immunoglobulin superfamily (1). The VSTM
family consists of 8 family members, each containing an immunoglobulin V-set (IgV)
domain in the extracellular domain (ECD).
In addition to the single IgV domain, VSTM2A contains two N-glycosylation
sites in the ECD that are critical for its secretion, but not for activity (2).
In humans, two isoforms exist due to alternative splicing, varying in the
C-terminal residues. The mature ECD of human VSTM2A, isoform 2 shares 80% amino
acid sequence identity with mouse and rat VSTM2A isoform 2. VSTM2A is expressed during adipocyte
development and its over-expression promotes adipogenesis (1). VSTM2A promotes
regulation and commitment of white and brown preadipocytes by increasing gene
expression of the transcription factor PPARG in a BMP4-dependent signaling
pathway (1, 2). VSTM2A is highly
expressed in the brain but the role
of VSTM2A in neuronal and brain development remain uncharacterized (3). VSTM2A
is a critical tumor suppressor in colorectal carcinogenesis and a novel
antagonist of Wnt signaling receptor LRP6, and might serve as a new prognostic
marker for colorectal cancer patients (4). Our in house data show that
VSTM2A inhibits the human T cell activation, including anti-CD3 induced IL-2
and IFN-gamma secretion, and T cell proliferation. Our Avi-tag Biotinylated VSTM2A
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.
- Secco, B. et al. (2017) Cell Rep. 18:93.
- Berry, D.C. et al. (2013) Development. 140:3939.
- Pandey, A.K. et al. (2014) PloS One. 9:e88889.
- Zhang,
D. et al. (2019) Theranostics. 9:6517.
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