Recombinant Human MUC-1 Fc Chimera Alexa Fluor® 488 Protein Summary
Details of Functionality |
Measured by flow cytometry for its ability to bind anti-Human MUC-1 Monoclonal Antibody conjugated beads.The concentration of Recombinant human MUC-1 Chimera Alexa Fluor® 488 (Catalog# AFG10332) that produces 50% of the binding response is 5.00-50.0 ng/mL |
Source |
Human embryonic kidney cell, HEK293-derived human MUC-1 protein Human MUC-1 (Ser24-Ser380) Accession # P15941.3 | IEGRMD | Human IgG1 (Pro100-Lys330) | N-terminus | | C-terminus | |
|
Accession # |
|
N-terminal Sequence |
Ser24 |
Structure / Form |
Disulfide-linked homodimer Labeled with Alexa Fluor® 488 via amines Excitation Wavelength: 488 nm Emission Wavelength: 515-545 nm |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<1.0 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
60 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 |
157-192 kDa, under reducing conditions. |
Packaging, Storage & Formulations
Storage |
Protect from light. Use a manual defrost freezer and avoid repeated freeze-thaw cycles. - 6 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after opening.
- 3 months, -20 to -70 °C under sterile conditions after opening.
|
Buffer |
Supplied as a 0.2 μm filtered solution in PBS with BSA as a carrier protein. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Notes
This product is provided under an agreement between Life Technologies Corporation and R&D Systems, Inc, and the manufacture, use, sale or import of this product is subject to one or more US patents and corresponding non-US equivalents, owned by Life Technologies Corporation and its affiliates. The purchase of this product conveys to the buyer the non-transferable right to use the purchased amount of the product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). The sale of this product is expressly conditioned on the buyer not using the product or its components (1) in manufacturing; (2) to provide a service, information, or data to an unaffiliated third party for payment; (3) for therapeutic, diagnostic or prophylactic purposes; (4) to resell, sell, or otherwise transfer this product or its components to any third party, or for any other commercial purpose. Life Technologies Corporation will not assert a claim against the buyer of the infringement of the above patents based on the manufacture, use or sale of a commercial product developed in research by the buyer in which this product or its components was employed, provided that neither this product nor any of its components was used in the manufacture of such product. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, Cell Analysis Business Unit, Business Development, 29851 Willow Creek Road, Eugene, OR 97402, Tel: (541) 465-8300. Fax: (541) 335-0354.
This product is provided under an agreement between Life Technologies Corporation and R&D Systems, Inc, and the manufacture, use, sale or import of this product is subject to one or more US patents and corresponding non-US equivalents, owned by Life Technologies Corporation and its affiliates. The purchase of this product conveys to the buyer the non-transferable right to use the purchased amount of the product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). The sale of this product is expressly conditioned on the buyer not using the product or its components (1) in manufacturing; (2) to provide a service, information, or data to an unaffiliated third party for payment; (3) for therapeutic, diagnostic or prophylactic purposes; (4) to resell, sell, or otherwise transfer this product or its components to any third party, or for any other commercial purpose. Life Technologies Corporation will not assert a claim against the buyer of the infringement of the above patents based on the manufacture, use or sale of a commercial product developed in research by the buyer in which this product or its components was employed, provided that neither this product nor any of its components was used in the manufacture of such product. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, Cell Analysis Business Unit, Business Development, 29851 Willow Creek Road, Eugene, OR 97402, Tel: (541) 465-8300. Fax: (541) 335-0354.
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human MUC-1 Fc Chimera Alexa Fluor® 488 Protein
Background
MUC-1 (Mucin-1) is a type 1 transmembrane glycoprotein that is normally
expressed on the apical surface of most epithelial cells (1, 2). It is known to be overexpressed by various
human carcinomas and is shed into circulation (2). The extracellular domain is made up of tandem
repeats (TRs) of 20 aa each, with each TR containing five potential
O-glycosylation sites (3). The number of TRs vary between 25-100, depending on
the allele (3). Within the mature region
including 16 TRs (residues 24-380), human MUC-1 shares 30% aa sequence identity
with mouse and rat MUC-1. It has been reported that high expression level of MUC-1
generally correlates with increased mortality rates (4). In addition, MUC-1 is
aberrantly underglycosylated on cancer cells with
short and sialylated
O-linked glycans in contrast to the long, branched chain seen in normal
epithelial cells (4-7). It has been demonstrated that MUC-1 can interact with
E-selectin and ICAM-1 to mediate firm adhesion of circulating tumor cells and
subsequent extravasation in the metastatic adhesion cascade (4). Furthermore, MUC-1 can modulate the tumor immunological
microenvironment through engagement of Siglec-9 by inducing the recruitment of
beta-catenin to the cytoplasmic
tail of MUC-1, increasing the expression of PD-L1 by macrophages, and activating
the MEK-ERK pathway (5, 6). MUC-1 can also interact with Galectin-3 to promote
EGFR activation thus regulating EGFR-associated tumorigenesis and cancer
progression (7).
- Rughetti, A. et al. (2005) J. Immunol. 174:7764.
- Engelstaedter, V. et al. (2012) BMC Cancer 12:600.
- Taylor-Papadimitriou, J. et al. (1999) Biochim. Biophys. Acta 1455:301.
- Geng, Y. et al. (2012) Front Oncol. 2:76.
- Tanida, S. et al. (2013) J Biol Chem. 288:31842.
- Beatson, R. et al. (2016) Nat Immunol. 17:1273.
- Piyush, T. et al. (2017) Cell Death Differ. 24:1937.
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