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Recombinant Human Mesothelin (aa 296-580) Fc Protein, CF

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When Recombinant Human CA125/MUC16  (5609-MU) is immobilized at 200 ng/mL (100 µL/well), Recombinant Human Mesothelin (aa 296-580) Fc Chimera Protein (Catalog # 10959-MS) binds with an ED50 of 1.00-6.00 ng/mL.
2 μg/lane of Recombinant Human Mesothelin C-Terminal (aa 296‑580) Fc Chimera Protein (Catalog # 10959-MS) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Human Mesothelin (aa 296-580) Fc Protein, CF Summary

Additional Information
C-Terminal
Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human CA125/MUC16   (Catalog # 5609-MU) is immobilized at 200 ng/mL (100 µL/well), Recombinant Human Mesothelin (aa 296-580) Fc Chimera binds with an ED50 of 1.00-6.00 ng/mL.
Source
Human embryonic kidney cell, HEK293-derived human Mesothelin protein
Human Mesothelin
(Glu296-Gly580)
Accession # AAH09272.1
IEGRMD Human IgG1
(Pro100-Lys330)
N-terminusC-terminus
Accession #
N-terminal Sequence
Glu296
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, 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
  • Bioactivity
Theoretical MW
59 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
65-80 kDa, 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.
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 Mesothelin (aa 296-580) Fc Protein, CF

  • CAK1 antigen
  • CAK1
  • megakaryocyte potentiating factor
  • Mesothelin
  • MPF
  • MPFSMRP
  • MSLN
  • Pre-pro-megakaryocyte-potentiating factor
  • SMR
  • soluble MPF mesothelin related protein

Background

Mesothelin (MSLN), also known as CAK1 and ERC, is a glycosylated cell-surface antigen present on normal mesothelial cells and over-expressed in several human tumors (1, 2). The mesothelin gene encodes a ~70 kDa precursor protein that is cleaved at a dibasic proteolytic site into a 40 kDa membrane-bound protein termed MSLN and a 31 kDa shed fragment called megakaryocyte-potentiating factor (MPF) that is released from the cell (3, 4). Cleaved, human MSLN remains attached to the cell surface via a GPI linkage and shares 58% amino acid sequence identity with mouse and rat MSLN. In human, alternate splicing generates additional MSLN isoforms that have either an eight amino acid insertion following Ser408 or a substituted C‑terminal region with no GPI anchor (3). Mesothelin is normally expressed on mesothelial cells in the pleura, pericardium, and peritoneum as well as in the developing and postnatal pancreas (1, 4). It is up‑regulated in mesotheliomas and a range of carcinomas and adenomas (5-7). Mesothelin promotes tumor cell proliferation, migration, anchorage-independent growth, and tumor progression (7, 8). It is co‑expressed with the tumor antigen CA125/MUC16 on advanced ovarian adenocarcinomas and interacts with this molecule to support cell adhesion (9). A soluble form of Mesothelin is released from tumor cells into the serum or tissue effusions (9-11).
  1. Hassan, R. et al. (2004) Clin. Cancer Res. 10:3937.
  2. Chang, K. and I. Pastan (1996) Proc. Natl. Acad. Sci. 93:136.
  3. Muminova, Z.E. et al. (2004) BMC Cancer 4:19.
  4. Hou, L.-Q. et al. (2008) Develop. Growth Differ. 50:531.
  5. Ordonez, N.G. (2003) Mod. Pathol. 16:192.
  6. Argani, P. et al. (2001) Clin. Cancer Res. 7:3862.
  7. Li, M. et al. (2008) Mol. Cancer Ther. 7:286.
  8. Uehara, N. et al. (2008) Mol. Cancer Res. 6:186.
  9. Rump, A. et al. (2004) J. Biol. Chem. 279:9190.
  10. Ho, M. and M.O. Lively (2006) Cancer Epidemiol. Biomarkers Prev. 15:1751.
  11. Robinson, B.W.S. et al. (2003) Lancet 362:1612.

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