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Recombinant Cynomolgus Mesothelin (aa417-693) His Protein CF

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When Recombinant Human CA125/MUC16 (5609-MU) is immobilized at 2.00 μg/mL (100 μg/well), Recombinant Cynomolgus Monkey Mesothelin C-Terminal (aa 417-693) His-tag (Catalog # 10764-MS) binds with an ED50 of 0.700-4.20 ...read more
2 μg/lane of Recombinant Cynomolgus Monkey Mesothelin (aa417-693) His-tag (Catalog # 10764-MS) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue ...read more

Product Details

Summary
Reactivity Pm-CmSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Cynomolgus Mesothelin (aa417-693) His 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 2.00 ug/mL (100 µL/well), Recombinant Cynomolgus Monkey Mesothelin C-Terminal (aa 417-693) His-tag protein binds with an ED50 of 0.700-4.20 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived cynomolgus monkey Mesothelin protein
Asp417-Asp693, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Asp417
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
32 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
35-45 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 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 Cynomolgus Mesothelin (aa417-693) His 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 overexpressed 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 cynomolgus MSLN remains attached to the cell surface via a GPI linkage and shares 84% amino acid sequence identity with human 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 upregulated in mesotheliomas and a range of carcinomas and adenomas (5-7). Mesothelin promotes tumor cell proliferation, migration, anchorage-independent growth, and tumor progression (8, 9). It is co-expressed with the tumor antigen CA125/MUC16 on advanced ovarian adenocarcinomas and interacts with this molecule to support cell adhesion (10). A soluble form of Mesothelin is released from tumor cells into the serum or tissue effusions (10-12).
  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. Li, M. et al. (2008) Mol. Cancer Ther. 7:286.
  9. Uehara, N. et al. (2008) Mol. Cancer Res. 6:186.
  10. Rump, A. et al. (2004) J. Biol. Chem. 279:9190.
  11. Ho, M. and M.O. Lively (2006) Cancer Epidemiol. Biomarkers Prev. 15:1751.
  12. Robinson, B.W.S. et al. (2003) Lancet 362:1612.

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