Measured by its binding ability in a functional ELISA. When rhLYPD3 is immobilized at 0.5 μg/mL (100 μL/well), rhGalectin-3 binds with an apparent K D <80 nM.
Source
Mouse myeloma cell line, NS0-derived human C4.4A/LYPD3 protein Leu31-His286, with a C-terminal 6-His tag
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<0.01 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Binding Activity
Theoretical MW
27.7 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
60-75 kDa, reducing conditions
Publications
Read Publication using 5428-C4 in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 degreesC as supplied. 1 month, 2 to 8 degreesC under sterile conditions after reconstitution. 3 months, -20 to -70 degreesC under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Reconstitution Instructions
Reconstitute at 100 μg/mL in sterile PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human C4.4A/LYPD3 Protein, CF
C4.4A
C4.4A2310061G07Rik
GPI-anchored metastasis-associated protein C4.4A homolog
GPI-anchored metastasis-associated protein homolog
LY6/PLAUR domain containing 3
ly6/PLAUR domain-containing protein 3
LYPD3
Matrigel-induced gene C4 protein
MIG-C4
Background
C4.4A, also known as Ly6/PLAUR domain containing 3 (LYPD-3), is a GPI-linked protein with structural similarity to the urokinase-type plasminogen activator receptor (uPAR) (1). It is a 65 - 100 kDa molecule with variable cell type-specific N- and O-linked glycosylation, and shares 80% amino acid sequence identity with mouse and rat C4.4A (2, 3). Mature human C4.4A contains two uPAR/Ly6 domains and a Ser/Thr/Pro-rich (STP) region that includes a protease sensitive site (4, 5). Proteolytic cleavage following the second uPAR/Ly6 domain generates a 35 - 40 kDa soluble form, while ADAM10 or ADAM17-mediated cleavage within the STP region generates a 90 kDa soluble form (6, 8). Soluble C4.4A can also be shed and released in membrane vesicles (5). C4.4A is expressed in the suprabasal layers of stratified squamous epithelium and is upregulated on migrating keratinocytes during wound healing (6, 7). Its expression is downregulated during the onset of epithelial dysplasia but is subsequently upregulated at the invasive front of melanomas and various carcinomas (2, 6, 5, 9). Metastases derived from these tumors also express high levels of C4.4A (2, 5, 6). The interaction of C4.4A with Laminin 1 and 5 on neighboring cells promotes the adhesion, spreading, and migration of tumor cells (4, 6, 10). C4.4A additionally interacts with Galectin-3 and the anterior gradient proteins AG-2 and AG-3 (10, 11). C4.4A overexpression in non-small cell lung cancer is predictive of increased mortality (12).
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Rosel, M. et al. (1998) Oncogene 17:1989.
Paret, C. et al. (2007) Br. J. Cancer 97:1146.
Smith, B.A. et al. (2001) Cancer Res. 61:1678.
Wurfel, J. et al. (2001) Gene 262:35.5.
Hansen, L.V. et al. (2008) Int. J. Cancer 122:734.
Hansen, L.V. et al. (2004) Biochem. J. 380:845.
Esselens, C.W. et al. (2008) Biol. Chem. 389:1075.
Seiter, S. et al. (2001) J. Invest. Dermatol. 116:344.
Paret, C. et al. (2005) Int. J. Cancer 115:724.
Fletcher, G.C. et al. (2003) Br. J. Cancer 88:579.
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