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  1. KRISHI Publication and Data Inventory Repository
  2. Animal Science A4
  3. ICAR-Indian Veterinary Research Institute D7
  4. AS-IVRI-Publication
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Please use this identifier to cite or link to this item: http://krishi.icar.gov.in/jspui/handle/123456789/17439
Title: Purification of Regucalcin from the Seminal Vesicular Fluid: A Calcium Binding Multi-Functional Protein
Other Titles: Not Available
Authors: Harikrishna, P., A. M. Shende, Reena K. K, Jobin Thomas, S. K. Bhure.
Published/ Complete Date: 2016-07-26
Project Code: Not Available
Keywords: Buffalo, Regucalcin, Purification, Seminal vesicular fluid, Affinity chromatography
Publisher: Springer
Citation: Not Available
Series/Report no.: Not Available;
Abstract/Description: Regucalcin is a multi-functional protein having roles in calcium homeostasis as well as in anti-apoptotic, anti-prolific and anti-oxidative functions. Recently, it has been reported from the male reproductive tract, but its role in male reproduction needs further investigation; for which the native regucalcin of reproductive origin will be more appropriate. The gel exclusion chromatography followed by diethyl aminoethane cellulose chromatography and twodimentional cellulose acetate membrane electrophoresis used for its purification are time consuming and less specific. Here, the regucalcin gene from buffalo testis has been cloned, expressed and purified in recombinant form, and subsequently used for raising hyper-immune serum. The Western blot of seminal vesicular fluid probed with antiregucalcin polyclonal and monoclonal antibodies showed the presence of 28 and 34 kDa bands specific to regucalcin. Further, an affinity matrix has been prepared using antiregucalcin polyclonal antibodies. An immuno-affinity chromatography method has been standardized to isolate regucalcin from seminal vesicular fluid. The initial complexity of the protein mixture in the seminal vesicular fluid has been reduced by a heat coagulation step. The purified protein on sodium dodecyl sulfate–polyacrylamide gel electrophoresis showed a single band at 68 kDa that has been further confirmed as regucalcin by Liquidchromatography–mass spectrometry/mass spectrometry. The RGN purified from seminal vesicular fluid will be more appropriate for studying its possible role in male reproduction, especially sperm cell capacitation, hyperactivation, acrosome reaction and cryopreservation. The study can be applied in purifying regucalcin from different tissues or species with minor modifications in the methodology.
Description: Not Available
ISSN: Not Available
Type(s) of content: Research Paper
Sponsors: ICAR-IVRI and CSIR
Language: English
Name of Journal: Protein Journal
NAAS Rating: 7.32
Volume No.: 35(4)
Page Number: 310-317
Name of the Division/Regional Station: Not Available
Source, DOI or any other URL: 10.1007/s10930-016-9674-x
URI: http://krishi.icar.gov.in/jspui/handle/123456789/17439
Appears in Collections:AS-IVRI-Publication

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