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33 results about "Podocalyxin" patented technology

Podocalyxin, a sialoglycoprotein, is thought to be the major constituent of the glycocalyx of podocytes in the glomerulus (Bowman's capsule). It is a member of the CD34 family of transmembrane sialomucins. It coats the secondary foot processes of the podocytes. It is negatively charged and thus functions to keep adjacent foot processes separated, thereby keeping the urinary filtration barrier open. This function is further supported by knockout studies in mice which reveal an essential role in podocyte morphogenesis and a role in the opening of vascular lumens and regulation of vascular permeability. Of note, this is the only cell surface sialomucin knockout known to display a lethal phenotype. Podocalyxin is also upregulated in a number of cancers and is frequently associated with poor prognosis. Sialylated, O-glycosylated glycoforms of podocalyxin expressed by colon carcinoma cells possess L-selectin and E-selectin binding activity, and may be pivotal to the metastatic spread of colon carcinoma cells. At the cellular level podocalyxin has also been shown to regulate the size and topology of apical cell domains and act as a potent inducer of microvillus formation.

Polymerase chain reaction detection method of urinary podocyte specific messenger ribonucleic acid (mRNA)

The invention provides a polymerase chain reaction detection method of urinary podocyte specific messenger ribonucleic acid (mRNA). The method is characterized by being established through the following steps of: collection of urine specimens; total RNA (ribonucleic acid) extraction as well as concentration and purity detection; reverse transcription; design and synthesis of primers; real-time PCR (polymerase chain reaction); preparation of a standard product and manufacture of a standard curve; and real-time PCR of the specimens to be detected and the standard product. The method has the characteristics of rapidness, simplicity and convenience, and can be used for acquiring an excellent quantitative linear correlation coefficient (R2>0.99); simultaneously, the established method is wide in detectable concentration range, podocalyxin and CD2-PA respectively spans 10 orders of magnitude and 8 orders of magnitude, and Ct values corresponding to minimum detectable concentrations of two types of genes respectively reach 35 and 33.2286; and furthermore, the inter-group and inter-batch differences of the high-concentration and light-concentration template Ct values, detected by the method, of the two types of genes are less than 3%, thus indicating that the method is high in stability and good in repeatability. The established method can be used for providing a stable technical platform for rapidly, simply and conveniently detecting the urinary podocyte specific mRNA.
Owner:SOUTHEAST UNIV
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