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Inositol Phosphates Analysis Service

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Inositol phosphates (IPs) are a group of mono to hexa-phosphorylated inositols. They play critical roles in diverse cellular functions including cell growth, apoptosis, cell migration, endocytosis and cell differentiation. Mono-, di-, and triphosphorylation of the inositol ring creates a wide range of stereochemically distinct signalling entities. For instance, inositol 1,4,5-trisphosphate (I(1,4,5)P3), is formed when the phosphoinositide phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) is hydrolysed by a phospholipase C isozyme. An array of inositol trisphosphate (IP3) and tetrakisphosphate (IP4) molecules are synthesised by the action of various kinases and phosphatases in the cytosol. These species then transport between the cytosol and the nucleus where they are acted on by inositol polyphosphate multikinase (IPMK), inositol-pentakisphosphate 2-kinase (IPPK), inositol hexakisphosphate kinase 1 (IP6K1) and 2 (IP6K2), to produce IP5, IP6, IP7, and IP8 molecules. As a carbohydrate metabolism, inositol phosphate metabolism plays important roles in mammalians. Thus, its dysfunction is closely associated with various diseases like Joubert syndrome and Centronuclear myopathy.

Inositol phosphates contain multiple phosphorylated derivatives and individual PIPs can contain different fatty acid chains, resulting in structural complexity. Creative Proteomics has built a dedicated analytical platform to provide you with qualitative and quantitative analysis of inositol phosphates. Based on ion chromatography separation techniques, we are able to accurately determine the total amount of phosphorylated derivatives. Based on LC/MS technology, we are able to quantify phosphatidylinositol containing specific fatty acid chain structures.

Advantages of Our Inositol Phosphates Analysis Service

State of the art facilities

Professional standard operation procedure

Low cost

Short experimental time

High accuracy, specificity, and sensitivity

Service Workflow

Inositol Phosphates Analysis Service

Inositol Phosphates Related Analytes That We Can Measure

Inositol monophosphateInositol bisphosphateInositol trisphosphate
Inositol pentakisphosphateInositol hexaphosphateMyo-inositol
BornesitolPhosphatidylinositol-3,4,5-trisphosphate (PIP3)Phosphatidylinositol 4,5-bisphosphate (PIP2)
1-Phosphatidyl-D-myo-inositol1-Phosphatidyl-1D-myo-inositol 3-phosphateD-myo-Inositol 1,3-bisphosphate
1D-myo-Inositol 3-phosphate1D-myo-Inositol 1,3,4,5,6-pentakisphosphate

Sample Requirements

We can analyze a wide range of biological materials including but not limited to cells and solid tissues from humans and animals, such as mice, rats, rabbits. If you need transport your samples to us, please follow the below requirements for different kinds of sample:

  • Blood/plasma: 500ul/sample
  • Urine: 1ml/sample
  • Tissue: 200mg/sample
  • Cells: 1x107/sample
  • Feces: 500mg/sample

Shipment condition: dry ice

We can also accept other types of samples, please contact our technical staff for details.

Report Delivery

  • Experimental procedures
  • The parameters of liquid chromatograph and mass spectrometer
  • HPLC and MS raw data files
  • Metabolite quantitative data

Creative Proteomics has extensive experience in the analysis of substances. We will provide accurate and detailed data and analysis reports. If you would like additional information or to test other substances, you can contact us. We are looking forward to working with you.

References

  1. Monserrate Jessica P, York John D. Inositol phosphate synthesis and the nuclear processes they affect. Curr Opin Cell Biol. 2010,22:365-373.
  2. Bunney Tom D, Katan Matilda. Phosphoinositide signalling in cancer: beyond PI3K and PTEN. Nat Rev Cancer. 2010.10:342-352.
  3. Bielas Stephanie L, Silhavy Jennifer L, Brancati Francesco, et al. Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies. Nat Genet. 2009,41:1032-1036.
  4. Agrawal Pankaj B, Pierson Christopher R, Joshi Mugdha, et al. SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy. Am J Hum Genet. 2014, 95:218-226.
For Research Use Only. Not for use in diagnostic procedures.
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