Product Catalog



Tetranectin / CLEC3B Antibody
| Catalog | Size (Price) | Quantity | In Stock | Operation | Other Information |
| 12735-MM05 |
|
YES |
|
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Tetranectin / CLEC3B Antibody Datasheet
| Order or Inquire for Tetranectin / CLEC3B Antibody product | Quality antibodies | Antibody production services | ||
| Detection limit is 0.039 ng/well in ELISA |
Tetranectin / CLEC3B Antibody Product Information
| Immunogen : |
Recombinant Human Tetranectin / CLEC3B protein (Catalog#12735-H08H) |
| Antibody Type : | Mouse Monoclonal Antibody ( Mouse mAb Service Platform ) |
|
Clone ID : |
05 |
| Ig Type : |
Mouse IgG2a |
| Formulation : | 0.2 μm filtered solution in PBS with 5% trehalose |
| Preparation : |
This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human Tetranectin / CLEC3B (rh Tetranectin / CLEC3B; Catalog#12735-H08H; AAX37102.1; Met 1-Val 202). The IgG fraction of the cell culture supernatant was purified by Protein A affinity chromatography. |
Tetranectin / CLEC3B Antibody Usage Guide
|
Specificity : |
Human Tetranectin / CLEC3B |
|
No cross-reactivity in ELISA with Human cell lysate (293 cell line) |
|
| Direct ELISA : | 6This antibody can be used at 0.5-1 μg/mL with the appropriate secondary reagents to detect Human CLEC3B. The detection limit for Human CLEC3B is approximately 0.039 ng/well. |
| Storage : | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -70℃. Preservative-Free. Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles. |
Tetranectin / CLEC3B Antibody Related Products & Topics
Related Areas:
Immunology>>Adhesion Molecule>>Lectin>>Tetranectin/CLEC3B
Proteins:
| Molecule | Species | Description //For Detailed Info. and Price------CLICK! | Cat. No |
| Tetranectin/CLEC3B | Human | Tetranectin/CLEC3B Protein, Recombinant | 12735-H08H |
| Tetranectin/CLEC3B | Mouse | Tetranectin/CLEC3B Protein, Recombinant | 50700-M08H |
Antibodies:
| Molecule | Application | Description //For Detailed Info. and Price------CLICK! | Cat. No |
| Human Tetranectin/CLEC3B | WB, ELISA | Tetranectin / CLEC3B Antibody | 12735-MM05 |
| Human Tetranectin/CLEC3B | WB, ELISA | Tetranectin / CLEC3B Antibody (Antigen Affinity Purified) | 12735-RP02 |
Tetranectin / CLEC3B Antibody Background
Tetranectin, also known as C-type lectin domain family 3, member B (CLEC3B), is a homotrimeric plasma and extracellular-matrix protein that binds plasminogen and complex sulphated polysaccharides including heparin. In terms of primary and tertiary structure, Tetranectin is related to the collectin family of Ca (2+)-binding C-type lectins. Tetranectin is encoded in three exons. Exon 3 encodes the carbohydrate recognition domain, which binds to kringle 4 in plasminogen at low levels of Ca (2+). Exon 2 encodes an alpha-helix, which is necessary and sufficient to govern the trimerization of Tetranectin by assembling into a triple-helical coiled-coil structural element. Tetranectin has been suggested to play a role in tissue remodeling, due to its ability to stimulate plasminogen activation and its expression in developing tissues such as developing bone and muscle. Tetranectin enhances plasminogen activation by a tissue-type plasminogen activator so that it has been suggested to play a role in tissue remodeling. TN may play a role in neurological diseases and may serve as a diagnostic aid in multiple sclerosis (MS). The serum or saliva Tetranectin may serve as a potential biomarker for metastatic oral squamous cell carcinoma (OSCC). Decreased plasma Tetranectin or increased Tetranectin in stroma of cancers correlates with cancer progression and adverse prognosis.
References
- Lorentsen RH, et al., 2000, Biochem J. 347 Pt 1: 83-7.
- Iba K, et al., 2001, Mol Cell Biol. 21 (22): 7817-25.
- Iba K, et al., 2009, Wound Repair Regen. 17 (1): 108-12.
- Stoevring B, et al., 2006, Scand J Clin Lab Invest. 66 (7): 577-83.
- Arellano-Garcia ME, et al., 2010, Int J Mol Sci. 11 (9): 3106-21.
- Mogues T, et al., 2004, J Biomed Biotechnol. 2004 (2): 73-8.

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