Reactivity | HuSpecies Glossary |
Applications | Bioactivity |
Details of Functionality | Measured in a cell proliferation/survival assay using IEC‑18 rat small intestinal epithelial cells. The ED50 for this effect is 0.6-2.4 μg/mL. |
Source | Chinese Hamster Ovary cell line, CHO-derived human Wnt-11 protein Ile25-Lys354 |
Accession # | |
N-terminal Sequence | Ile25 |
Protein/Peptide Type | Recombinant Proteins |
Gene | WNT11 |
Purity | >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. |
Dilutions |
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Theoretical MW | 36.6 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. |
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SDS-PAGE | 38-40 kDa, reducing conditions |
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Publications |
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Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Buffer | Lyophilized from a 0.2 μm filtered solution in PBS, EDTA and CHAPS with BSA as a carrier protein. |
Purity | >95%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Reconstitution Instructions | Reconstitute at 100 μg/mL in PBS containing at least 0.1% human or bovine serum albumin. |
Wnt‑11 belongs to the Wnt family of secreted, highly conserved, cysteine-rich cell signaling glycoproteins that play important roles in vertebrate developmental pattern formation, cell fate decision, axon guidance, and tumor formation (1-3). Mature human Wnt‑11 shares 98% amino acid (aa) sequence identity with mouse, rat and bovine Wnt‑11, and 99%, 96% and 88% aa identity with canine, equine and chick Wnt‑11, respectively. Mouse Wnt‑11 is expressed in early development during gastrulation and in the perichondrium, lung mesenchyme and ureteric buds, but not in neuroepithelium (1). It is required for cardiogenesis, organization of early muscle fibers, and branching morphogenesis of ureters (3-7). It is also expressed in several human cancers (2). In vitro, Wnt‑11 has been shown to induce cardiomyocyte differentiation from unfractionated mouse bone marrow mononuclear cells, and to promote hematopoietic differentiation from human embryoid body stem cells by engaging Frizzled-7 in the presence of E-cadherin (6, 8). In general, there are three signaling pathways associated with Wnt‑receptor interaction. The canonical pathway results in beta -Catenin accumulation and TCF/LEF‑1‑mediated gene transcription. Non‑canonical pathways include the Wnt/Ca2+ pathway and the planar cell polarity (PCP) pathway. Wnt‑11 often, but not exclusively, signals by a non‑canonical pathway and may repress canonical signaling by other Wnts (2, 9). However, when complexed with Wnt‑5a, Wnt‑11 can also enhance canonical signaling (10).
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