Podoplanin (D9D7) Rabbit mAb (BSA and Azide Free) #17758
- WB
- F
Supporting Data
| REACTIVITY | H |
| SENSITIVITY | Endogenous |
| MW (kDa) | 36 |
| Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- F-Flow Cytometry
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
This formulation is ideal for use with technologies requiring specialized or custom antibody labeling, including fluorophores, metals, lanthanides, and oligonucleotides. It is not recommended for ChIP, ChIP-seq, CUT&RUN or CUT&Tag assays. If you require a carrier free formulation for chromatin profiling, please contact us. Optimal dilutions/concentrations should be determined by the end user.
Formulation
Storage
Specificity / Sensitivity
Species Reactivity:
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Asp31 of human podoplanin protein.
Background
Podoplanin (aggrus, glycoprotein 36) is a single-pass transmembrane protein belonging to the type-1 family of sialomucin-like glycoproteins. Podoplanin was first described in the rat as a surface glycoprotein that regulated podocyte morphology (1). It is now commonly used as a marker of lymphatic endothelial cells, where its expression is associated with the process of lymphangiogenesis (2). Its role in this regard is presumably due to its putative involvement in regulating actin cytoskeleton dynamics (3). Research studies have shown that podoplanin expression is upregulated in a number of tumor types including colorectal cancers (4), oral squamous cell carcinomas (5), and germ cell tumors (6), with higher expression levels often associated with more aggressive tumors (7). Research studies have suggested a functional role for podoplanin in the stromal microenvironment of tumors. For example, it has been reported that podoplanin expression in cancer-associated fibroblasts (CAFs) is positively associated with a stromal environment that promotes cancer progression (8,9).
- Breiteneder-Geleff, S. et al. (1997) Am J Pathol 151, 1141-52.
- Breiteneder-Geleff, S. et al. (1999) Am J Pathol 154, 385-94.
- Wicki, A. et al. (2006) Cancer Cell 9, 261-72.
- Omachi, T. et al. (2007) Cancer Lett 246, 167-72.
- Feng, J.Q. et al. (2012) Oral Oncol 48, 848-852.
- Mishima, K. et al. (2006) Acta Neuropathol 111, 563-8.
- Raica, M. et al. Anticancer Res 28, 2997-3006.
- Schoppmann, S.F. et al. (2012) Breast Cancer Res Treat 134, 237-44.
- Ito, M. et al. (2012) Chest 142, 151-158.
限制使用
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