>90%, 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
Bioactivity not tested
Theoretical MW
73 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
90-108 kDa, reducing conditions
Publications
Read Publication using 9688-CU in the following applications:
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
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 250 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 Mouse CDCP1 Protein, CF
CD318 antigen
CD318
CDCP1
CUB domain containing protein 1
CUB domain-containing protein 1
Membrane glycoprotein gp140
SIMA135
SIMA135TRASK
Subtractive immunization M plus HEp3-associated 135 kDa protein
Transmembrane and associated with src kinases
Background
CDCP1 (CUB-domain containing protein 1; also known as CD318
and SIMA135) is a novel, 135 kDa cell surface glycoprotein that is found
on tumor, stem cells, keratinocytes and colonic epithelial cells (1). It is
reported that this protein is over-expressed in colon and lung cancers. CDCP1 is
a type I transmembrane (TM) protein that is involved with cell adhesion. Mouse
CDCP1 is synthesized as an 833 amino acid (aa) precursor. It contains an
extracellular region with three CUB domains (aa 30‑667) and a
phosphotyrosine site at Tyr731. The phosphorylation state of CDCP-1 has an
effect on anchorage in epithelial cells (2). When unligated, CDCP1 can be proteolytically
cleaved between aa 270‑300. This generates an 80 kDa TM protein that
may be missing the N-terminal CUB domain (aa 221‑350) (3). Over aa 25‑667,
mouse CDCP1 is 83% and 92% aa identical to human and rat CDCP1,
respectively.
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