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Prostaglandin F-biotin

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    Prostaglandin F<sub>2α</sub>-<wbr/>biotin
  • Prostaglandin F<sub>2α</sub>-<wbr/>biotin
Cat No: 10006988
Cayman
€70.00
Price is excluding VAT and does not include packaging neither shipping

Prostaglandin F2α-biotin (PGF2α-biotin) is an affinity probe which allows PGF2α to be detected through an interaction with the biotin ligand. PGF2α-biotin was designed to allow PGF2α to be detected in complexes with transmembrane receptors and/or nucle...

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Territorial Availability: Available through Bertin Technologies only in Europe
Synonyms:
  • 9α,11α,15S-trihydroxy-prosta-5Z,13E-dien-1-oyl-N'-biotinoyl-1,5-diaminopentane
  • PGF2α-biotin
Correlated keywords:
  • prostaglandins
  • biotinimides
  • eicosanoids
  • COX-1
  • COX-2
  • cyclooxygenases
  • reproductive
  • tissues
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Product Overview:
Prostaglandin F2α-biotin (PGF2α-biotin) is an affinity probe which allows PGF2α to be detected through an interaction with the biotin ligand. PGF2α-biotin was designed to allow PGF2α to be detected in complexes with transmembrane receptors and/or nucleic acid or protein binding partners. It is thus a tool to be used in the general elucidation of the mechanism of action of PGs.
Prostaglandin F2α (PGF2α) is the major eicosanoid product of cyclooxygenase-1 and 2 in reproductive tissues, and many others. PGF2α contracts bronchial smooth muscle, and regulates fertility and implantation. PGF2α acts through the FP receptor, a 7-transmembrane G-protein coupled receptor. PGF2α-biotin is an affinity probe which allows PGF2α to be detected through an interaction with the biotin ligand. PGF2α-biotin was designed to allow PGF2α to be detected in complexes with transmembrane receptors and/or nucleic acid or protein binding partners. It is thus a tool to be used in the general elucidation of the mechanism of action of PGs.
Size 50 µg
Shipping wet ice
Stability Store at -20 degrees; shelf life 365 days maximum after production
Molecular Formula C35H60N4O6S
SMILES CCCCC[C@H](O)/C=C/[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(NCCCCCNC(CCCC[C@H]2SC[C@@](N3[H])([H])[C@]2([H])N([H])C3=O)=O)=O
Molecular Weight 664.9
Formulation A solution in ethanol
Purity ≥96%
Custom Code 2937500000
UNSPSC code 12352100
UN Number UN1170

Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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