Recombinant Human LECT2 Protein, CF Summary
| Details of Functionality |
Measured in a cell proliferation assay using MC3T3-E1 mouse preosteoblast cells. The ED50 for this effect is 0.8-4.8 μg/mL.
|
| Source |
Human embryonic kidney cell, HEK293-derived human LECT2 protein Gly19-Leu151 |
| Accession # |
|
| N-terminal Sequence |
Gly19 |
| 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 |
|
| Theoretical MW |
15 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 |
15-17 kDa, reducing conditions |
Packaging, Storage & Formulations
| Storage |
- 12 months from date of receipt, ≤ -20 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 3 months, ≤ -20 °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 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 Human LECT2 Protein, CF
Background
LECT2
(leukocyte cell-derived chemotaxin-2), also known as Chondromodulin-II, is a neutrophil
chemotactic protein predominantly expressed in the liver (1).
It was first identified in the heparin-binding
components extracted from fetal bovine epiphyseal cartilage (2). Human LECT2
cDNA encodes a 151 amino acid (aa) precursor that includes an 18 aa signal
sequence (3). The mature human LECT2 is a 16 kDa secreted hepatic protein that
has a putative peptidase-M23 domain (3, 4). Human LECT2 shares 87% and 86% aa
sequence identity with mouse and rat LECT2, respectively. LECT2 stimulates the growth and matrix formation
of chondrocytes
in vitro (2, 5, 6). In
MC3T3-E1 cells, it promotes proliferation but inhibits alkaline
phosphatase activity (5, 6).
In vivo study suggested LECT2 can directly suppress the development of type II collagen antibody–induced arthritis (4). Recent studies have shown that LECT2 is an important regulator
of tumor growth during hepatocellular
carcinoma development and progression; it inhibits the angiogenic effect of HUVECs
in vitro and
in vivo (7).
- Yamagoe, S. et al. (1996) Immunol. Lett. 52:9.
- Hiraki, Y. et al. (1996) J. Bio. Chem. 271:22657.
- Slowik, V. and U. Apte (2017) Clin. Transl. Sci. 10:249.
- Okumura, A. et al. (2013) FEBS Lett. 587:404.
- Mori, Y. et al. (1997) FEBS Letters 406:310.
- Shukunami, C. et al. (1999) J. Biochem. 125:436.
- Chen, C.K. et al. (2016) Sci. Rep. 6:31398.
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