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Wortmannin, (PI3 Kinase inhibitor)

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号:12-338

牌:Millipore 密理博

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Replacement Information
Description
Catalogue Number 12-338
Brand Family Upstate
Trade Name
  • Upstate
Description Wortmannin, (PI3 Kinase inhibitor)
Overview Wortmannin, a fungal metabolite, is a cell-permeable, irreversible inhibitor of phosphatidylinositol 3 kinase (PI3 Kinase) with an IC50 of 5nM. It blocks the catalytic activity of PI3-Kinase without affecting upstream signaling events such as insulin receptor tyrosine kinase activity. Wortmannin also inhibits the activities of myosin light chain kinase and PI4-Kinase at concentrations a hundred times higher than those required to inhibit PI3-Kinase.
References
Product Information
Presentation 1mg of lyophilized powder packaged under inert gas. White to off-white powder.
Applications
Application The Wortmannin, (PI3 Kinase inhibitor) controls the biological activity of PI3 Kinase. This small molecule/inhibitor is primarily used for Biochemicals applications.
Key Applications
  • Kinase Assay
Biological Information
Entrez Gene Number
Entrez Gene Summary Receptor-regulated class I phosphoinositide 3-kinases (PI3Ks) phosphorylate the membrane lipid phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2) to PtdIns(3,4,5)P3, which in turn recruits and activates cytosolic effectors involved in proliferation, survival, or chemotaxis. PIK3R5 is a PI3K regulatory subunit (Brock et al., 2003 [PubMed 12507995]).[supplied by OMIM]
Gene Symbol
  • PIK3R5
  • P101-PI3K
  • FOAP-2
  • F730038I15Rik
Protein Target PI3Kγ
Target Sub-Family PI3K/PI4K
UniProt Number
UniProt Summary FUNCTION: SwissProt: Q8WYR1 # Regulatory subunit of the PI3K gamma complex.
SIZE: 880 amino acids; 97348 Da
SUBUNIT: Heterodimer of a catalytic subunit (PIK3CG/p120) and a regulatory (PIK3R5a/p101) subunit. Interacts with G beta gamma proteins.
SUBCELLULAR LOCATION: Nucleus (By similarity). Cytoplasm (By similarity). Membrane; Peripheral membrane protein (By similarity).
TISSUE SPECIFICITY: Highly expressed in leukocytes, followed by spleen, lymph node, thymus ans bone marrow.
DOMAIN:SwissProt: Q8WYR1 The heterodimerization region allows the binding to the catalytic subunit.
SIMILARITY:
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Quality Assurance Routinely evaluated by kinase assay.
Purity: ≥95% by HPLC.
Molecular Formula: C23H24O8
Molecular Weight: 428.4
Usage Statement
  • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage and Shipping Information
Storage Conditions Protect from light. Stable for 2 years as supplied at -20°C. Following reconstitution aliquot and store at -20°. The DMSO/ethanol stock solutions are stable for 1-3 months at -20°C.
Packaging Information
Material Size 1 mg
Transport Information
Supplemental Information
Specifications

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