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Dissertations / Theses on the topic 'Seminal vesicles'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

陳德華 and Tak-wah Chan. "Epithelial-mesenchymal interactions in development and cytodifferentiation of seminal vesicle." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1994. http://hub.hku.hk/bib/B31211239.

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Chan, Tak-wah. "Epithelial-mesenchymal interactions in development and cytodifferentiation of seminal vesicle /." Hong Kong : University of Hong Kong, 1994. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13762692.

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3

Williams, R. L. "Organisation and control of androgen-responsive genes of rat seminal vesicles." Thesis, University of Leeds, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355711.

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4

Schultheiss, Willem Andreas. "Some aspects of the aetiology of vesiculitis in a Sussex herd." Pretoria : [s.n.], 1998. http://explore.up.ac.za/record=b1411086.

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5

Tam, Chuen-chu. "Hormonal effects of the lateral prostate and seminal vesicle of the guinea pig : an ultrastructural, morphometric and cytochemical study /." Hong Kong : University of Hong Kong, 1989. http://sunzi.lib.hku.hk/hkuto/record.jsp?B12418833.

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6

Silva, Yamê Fabres Robaina Sancler da [UNESP]. "Efeito do tratamento local de vesiculite seminal sobre a qualidade e longevidade so sêmen equino." Universidade Estadual Paulista (UNESP), 2014. http://hdl.handle.net/11449/110631.

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Made available in DSpace on 2014-11-10T11:09:54Z (GMT). No. of bitstreams: 0 Previous issue date: 2014-02-26Bitstream added on 2014-11-10T11:57:43Z : No. of bitstreams: 1 000789914.pdf: 1497556 bytes, checksum: 733d284c8aacfd301e7a417adb15a971 (MD5)<br>A vesiculite seminal possui grande relevância na clínica reprodutiva devido à dificuldade de tratamento, elevados índices de recidiva, risco de contaminação de fêmeas com agentes patogênicos, inutilização de animais e baixos índices de fertilidade. O tratamento local tem sido apontado por diversos autores como a melhor alternativa terapêutica,

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Silva, Yamê Fabres Robaina Sancler da. "Efeito do tratamento local de vesiculite seminal sobre a qualidade e longevidade so sêmen equino /." Botucatu, 2014. http://hdl.handle.net/11449/110631.

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Orientador: Frederico Ozanam Papa<br>Banca: João Carlos Pinheiro Ferreira<br>Banca: André Maciel Crespilho<br>Resumo: A vesiculite seminal possui grande relevância na clínica reprodutiva devido à dificuldade de tratamento, elevados índices de recidiva, risco de contaminação de fêmeas com agentes patogênicos, inutilização de animais e baixos índices de fertilidade. O tratamento local tem sido apontado por diversos autores como a melhor alternativa terapêutica, porém nenhum estudo avaliou seus efeitos na qualidade e longevidade seminal. Nesse sentido, os objetivos do presente estudo incluíram: i

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8

Davey, Tamara. "Functional characterisation of a novel osteoclast-derived factor." University of Western Australia. School of Surgery and Pathology, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0219.

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[Truncated abstract] Intracellular communication between osteoclasts and osteoblasts is imperative to maintain bone integrity. A myriad of molecules are responsible for regulating osteoblast and osteoclast activity. In particular, it is well documented that osteoblast-derived factors are crucial in directly controlling osteoclast formation and function. Since bone formation is coupled to bone resorption, it would be expected that osteoclasts also have some role in regulating the growth and function of osteoblast cells. However, despite extensive research upon osteoclast and osteoblast biology,

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9

Sahlén, Göran. "Formation,Storage and Secretion of Prostasomes in Benign and Malignant Cells and Their Immunogenicity in Prostate Cancer Patients." Doctoral thesis, Uppsala University, Department of Surgical Sciences, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7511.

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<p>Prostasomes are submicron-sized, membrane-bound organelles produced by the epithelial cells of the prostate and normally found in the secretion in the gland ducts. Their physiological role is in the promotion of sperm-function in human reproduction. This thesis contains four papers dealing with the production of prostasomes and some possible applications in clinical urology of the prostasome. </p><p>Paper I and II provided an ultrastructural description of the synthesis, storage and secretion of prostasomes in benign as well as in malignant tissue. Most notable were the extracellular appear

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10

陳良 and Leung Franky Chan. "A morphological, histochemical and experimental study of the prostate gland and seminal vesicles of the guinea pig, with special referenceto the stroma." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1989. http://hub.hku.hk/bib/B30425773.

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11

Kim, Julie M. "Androgen-induced norepinephrine release in male accessory sex organ smooth muscle growth and differentiation." Morgantown, WV : [West Virginia University Libraries], 1999. http://etd.wvu.edu/templates/showETD.cfm?recnum=417.

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Thesis (Ph. D.)--West Virginia University, 1999.<br>Title from document title page. Document formatted into pages; contains vi, 125 p. : ill. Vita. Includes abstract. Includes bibliographical references (p. 107-122).

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12

Chan, Leung Franky. "A morphological, histochemical and experimental study of the prostate gland and seminal vesicles of the guinea pig, with special reference to the stroma /." [Hong Kong : University of Hong Kong], 1989. http://sunzi.lib.hku.hk/hkuto/record.jsp?B12439794.

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13

譚銓株 and Chuen-chu Tam. "Hormonal effects of the lateral prostate and seminal vesicle of the guinea pig: an ultrastructural, morphometricand cytochemical study." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1989. http://hub.hku.hk/bib/B3123169X.

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14

Barrachina, Villalonga Ferran. "Proteòmica del plasma seminal i de les seves vesícules extracel·lulars: nova font de biomarcadors útils en l’estudi de la funció espermàtica i la infertilitat masculina." Doctoral thesis, Universitat de Barcelona, 2020. http://hdl.handle.net/10803/672925.

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La infertilitat és un problema freqüent a escala mundial cada cop més comú. No obstant això, la manca de comprensió de la biologia reproductiva masculina i dels mecanismes moleculars alterats en pacients infèrtils resulta en una disponibilitat limitada i insuficient d’eines diagnòstiques i pronòstiques per a l’avaluació de la fertilitat masculina, així com de tractaments per a la infertilitat. Tot i que l’espermatozoide és la peça clau en la transmissió de la informació paterna a l’embrió, hi ha evidències que els fluids secretats per l’epidídim i les glàndules sexuals accessòries, incloent-hi

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15

Кравчук, О. М. "Вплив гіпертермії різного ступеня на органометричні параметри сім'яних пухирців статевонезрілих щурів". Thesis, Сумський державний університет, 2015. http://essuir.sumdu.edu.ua/handle/123456789/41704.

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16

NUGYEN, QUOC HIEN GEORGES. "Imagerie des vesicules seminales." Lille 2, 1990. http://www.theses.fr/1990LIL2M242.

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17

BUTTIN, FRANCOIS-XAVIER. "Vesiculectomie seminale : comment, pourquoi ?" Lyon 1, 1994. http://www.theses.fr/1994LYO1M055.

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18

Fawell, S. E. "Androgenic regulation of secretory protein synthesis in rat seminal vesicle." Thesis, University of Leeds, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355701.

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19

Kessler, Damien. "L'adenocarcinome des vesicules seminales : a propos de deux cas : revue de la litterature." Université Louis Pasteur (Strasbourg) (1971-2008), 1991. http://www.theses.fr/1991STR1M199.

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20

呂小楓 and Xiaofeng Lu. "Changes in cytodifferentiation of the dunning prostatic adenocarcinomainduced by neonatal rat seminal vesicle mesenchyme." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1998. http://hub.hku.hk/bib/B31215610.

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21

Lu, Xiaofeng. "Changes in cytodifferentiation of the dunning prostatic adenocarcinoma induced by neonatal rat seminal vesicle mesenchyme /." Hong Kong : University of Hong Kong, 1998. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19852216.

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22

Seidensticker, Mathias [Verfasser]. "Drug Effects on the Excretory Ductal System of the Prostate, Seminal Vesicle and Epididymis / Mathias Seidensticker." Gießen : Universitätsbibliothek, 2020. http://d-nb.info/1209159805/34.

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23

COLUNA, João Marcelo Martins. "Efeitos do uso de probiótico sobre a toxicidade do dicromato de potássio no sistema reprodutor masculino e adrenais de ratos Wistar." Universidade do Oeste Paulista, 2014. http://bdtd.unoeste.br:8080/jspui/handle/jspui/1050.

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Submitted by Adriana Martinez (amartinez@unoeste.br) on 2017-08-31T20:12:04Z No. of bitstreams: 1 João Marcelo Martins Coluna.pdf: 316916 bytes, checksum: e3ff1f0c4795f8a26f2d99c916a84f41 (MD5)<br>Made available in DSpace on 2017-08-31T20:12:04Z (GMT). No. of bitstreams: 1 João Marcelo Martins Coluna.pdf: 316916 bytes, checksum: e3ff1f0c4795f8a26f2d99c916a84f41 (MD5) Previous issue date: 2014-03-24<br>The aim of this study was to evaluate the effect of probiotics on the toxicity of increasing doses of potassium dichromate on the reproductive tract and adrenal glands of rats . Material and Me

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24

Wong, Pik-fan, and 黃碧芬. "The effects of castration and testosterone replacement on the gene expression of adrenomedullin and its receptor component proteins inthe rat epididymis, seminal vesicle and coagulating gland." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B42924613.

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BROCHARD, DENIS. "Etude structurale et fonctionnelle du promoteur du gene codant pour une proteine de secretion de la vesicule seminale de souris." Clermont-Ferrand 2, 1998. http://www.theses.fr/1998CLF22035.

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Le gene codant pour msvsp99 (mouse seminal secretory protein of 99 amino-acids) est specifiquement exprime dans la vesicule seminale de souris, et est regulee au niveau transcriptionnel par les androgenes. Une analyse fonctionnelle des sequences 5 flanquantes du gene de msvsp99, conduite par transfection transitoire en cellules cv1, a permis de delimiter la region proximale 387/+16 comme etant suffisante pour conferer une expression androgeno-dependante au rapporteur cat. La recherche d'elements de reponse aux androgenes sur cette region par des techniques d'interaction adn/proteines a l'aide

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26

Wong, Pik-fan. "The effects of castration and testosterone replacement on the gene expression of adrenomedullin and its receptor component proteins in the rat epididymis, seminal vesicle and coagulating gland." Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B42924613.

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27

GUILBAUD, CECILE. "Etude de l'expression et de la regulation au cours du developpement de proteines androgeno-dependantes de la vesicule seminale de souris." Clermont-Ferrand 2, 1994. http://www.theses.fr/1994CLF21639.

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L'etude de l'ontogenese de 3 proteines androgeno-dependantes de la vesicule seminale (de poids moleculaires 15. 5, 120 et 140 kd) et de mvdp (mouse vas deferens protein) dans le canal deferent montre que mvdp est accumulee a 20 jours, la proteine de 15. 5 kd a partir de 30 jours alors que les proteines de 120 et 140 kd n'apparaissent et ne sont accumulees qu'entre 30 et 40 jours. L'augmentation importante du taux de ces 4 proteines n'est pas correlee a des changements quantitatifs ou qualitatifs en androgenes tissulaires. La modification experimentale des concentrations hormonales (castration

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28

NORMAND, THIERRY. "Etude experimentale du role des androgenes dans l'expression des proteines de la vesicule seminale de souris a l'age et au cours du developpement." Clermont-Ferrand 2, 1991. http://www.theses.fr/1991CLF21252.

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L'analyse electrophoretique sds-page montre que parmi la cinquantaine de bandes proteiques revelees, dix sont induites par les androgenes alors que huit autres sont seulement exprimees chez des animaux castres (proteines reprimees). Les effets negatifs de la castration peuvent etre abolis completement par l'administration de testosterone ou dht. Les proteines induites par les androgenes apparaissent de facon sequentielle au cours du developpement. Les proteines reprimees presentes a 10 jours d'age, disparaissent apres le 40#e jour. L'ontogenese prepubaire des proteines androgeno-dependantes pe

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29

Chaulin, Bertrand. "Imagerie par résonance magnétique dans le bilan d'extension du cancer de la prostate aux vésicules séminales." Bordeaux 2, 1991. http://www.theses.fr/1991BOR23003.

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30

SIMON, ANNE-MARIE. "Etude de l'expression au cours du developpement et a l'age adulte de deux arnm androgeno-dependants de la vesicule seminale de souris. Isolement et caracterisation d'un des genes correspondant : msvsp99." Clermont-Ferrand 2, 1995. http://www.theses.fr/1995CLF21734.

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Les adnc de deux messagers exprimes dans les vesicules seminales de souris (mouse seminal vesicle secretory protein of 99 aminoacids - msvsp99 et seminal vesicle secretory protein iv - svs iv) ont ete caracterises. La comparaison de leur sequence avec celles contenues dans les banques de donnees a montre qu'ils appartiennent a la famille des svs (seminal vesicle secretory protein), proteines des vesicules seminales du rat et de la souris impliquees dans les phenomenes de fertilite. Le gene de msvsp99 a ete isole: il s'etend sur 1700 pb et est divise en 4 exons. La region promotrice du gene con

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31

CAI, WEI-BO, and 蔡偉博. "Characterization of seminal vesicles autoantigen (SVA)." Thesis, 1991. http://ndltd.ncl.edu.tw/handle/03428763624300790619.

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32

Hwang, Yan-Hwa, and 黃彥華. "Biochemical Characterization of the Mouse Seminal Vesicles Autoantigen (SVA)." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/3aer8f.

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Ching-wei, Luo, and 羅清維. "Biochemical Characterization of the Mouse Seminal Vesicles Autoantigen (SVA)." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/80056083017870657226.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>82<br>Mouse seminal vesicle autotigen (SVA) has been identified recently from our laborary. It is a 19 kDa glycoprotein and the primary structure of tis protein core has been established by cDNA cloning and proyein sequening. The main task fo this work is to study the structure and the function of SVA. The protein was estimated to contain 25 % beta-structure and no helical structure on the basis of its CD. The complex formation of SVA and zinc ion caused no change

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34

CHEN, JIN-LONG, and 陳金龍. "Autoimmunization and isoimmunization of mouse seminal vesicle secretion:isolation and characterization of seminal vesicle autoantigens (SVA)." Thesis, 1990. http://ndltd.ncl.edu.tw/handle/17327474122678963264.

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35

WANG, BEN-NEN, and 王本甯. "Studies of Mouse Seminal Vesicle Autoantigen Promoter." Thesis, 1998. http://ndltd.ncl.edu.tw/handle/54964076007150367955.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>86<br>Semen comes mainly from the secretions of seminal vesicle and other accessory glands. An autoantigen，the seminal vesicle autoantigen (SVA)，has been purified from seminal vesicle secretion. It is a 19 kDa androgen-dependent glycoprotein. The preliminary data from our laboratory indicate that SVA is a sperm mobility inhibitor with the ability to suppress the BSA-induce sperm capacitation. By comparison，ten potential androgen response elements (AREs) have been

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Yu, Long-Chih, and 余榮熾. "Biochemical Study of Mouse Seminal Vesicle Autoantigen." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/95043587554996347992.

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博士<br>國立臺灣大學<br>生化科學研究所<br>82<br>A protein extract of mouse seminal vesicle secretion was used to immunize mature mice (BALB/c) of both sexes. Results of Western analyses for these secretory proteins indicated that only one minor protein component could be recognized by the autoantisera prepared from either autoimmunization of male mice or isoimmunization of female mice. The autoantigen was purified from seminal vesicle secretion. The autoantigen has glycoprotein characteristics: the majori

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CHEN, XUAN-FEI, and 陳璿妃. "Studies on seretory protease inhibitors of mouse seminal vesicle." Thesis, 1989. http://ndltd.ncl.edu.tw/handle/54070237151370028940.

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Ya-Ling, Hsiao, and 蕭雅鈴. "The Genomic Structure of A Mouse Seminal Vesicle Autoantigen." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/93844826902645080667.

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39

Shu, Jye-An, and 徐捷安. "Regulation Mechanism of Seminal Vesicle Autoantigen on Mouse Sperm Capacitation." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/42056614802740899594.

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碩士<br>臺北醫學大學<br>醫學研究所<br>96<br>Capacitation processes are complex biological events for sperm to aquire the ability for fertilization. It was tightly regulated by capacitation factors and decapacitation factors. Many attempts have been shown to demonstrate the capacitation mechanisms; however, the decapacitation regulation remains unclear. In the past ten years, our lab has been demonstrated a seminal vesicle autoantigen (SVA), a novel 19 kDa phospholipids-binding protein in seminal plasma, could play a role as a decapacitation factor to suppress the capacitation factor (like BSA, PAF, and cyc

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KUO, SHIN-PEI, and 郭欣珮. "Decapacitation Mechanism of Sperm Induced by Mouse Seminal Vesicle Autoantigen." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/60177925994152174664.

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碩士<br>臺北醫學大學<br>醫學研究所<br>92<br>Sperm capacitation involves a complex biological molecular event to acquire the capacity for acrosome reaction and fertilization. During the transit of sperm from male testis to female oviduct, capacitation should take place at right time and right place in the reproductive tract after ejaculation. Factors promoted or inhibited sperm activity should interplay to prevent the gamete prematuriza- tion. Recently, the molecular events associated with capacitation are well documented, but less progress has been made to study the decapacitation effect. Here, we demonstr

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CHEN, XI-DI, and 陳希迪. "Anandrogen-dependent Kazal type trypsin inhibitor from mouse seminal vesicle." Thesis, 1992. http://ndltd.ncl.edu.tw/handle/86184828961370258874.

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TSENG, HUAN-CHIN, and 曾煥清. "Study of mouse SVS I protein in mouse seminal vesicle secretion." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/50863159613582794136.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>91<br>The genomic structure of MpSv-2, a novel androgen-regulated gene exclusively expressed in mouse seminal vesicle, was analyzed to establish a 5-flanking region of 2002 bp, five exons of 2038、277、134、139 and 133 bp and 4 introns of 1060、278、240 and 509 bp.The length of MpSv-2 cDNA is 2733bp.The putative MpSv-2 translate protein contains 820 amino aids that sum to give a molecular mass of 90,200 Da. The translate protein was predicted to a secretory protein and the molecular mass of MpSv-2 translate protein is similar to mouse seminal vesicle secretion

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Guo, Hong-Wen, and 郭鴻文. "Physiological Study of a Trypsin Inhibitor from Mouse Seminal Vesicle Secretion." Thesis, 1998. http://ndltd.ncl.edu.tw/handle/18323136940431232478.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>86<br>A kazal-type trypsin inhibitor (TI) has been previously purified from seminal vesicle secretion in our laboratory. The protein contains no carbohydrate and its molecular weight is 6.4 kDa as estimated by SDS-electrophoresis. Among the reproductive tracts of mice, TI is product only male accessory sexual gland such as seminal vesicles, prostate and coagulating gland. This work aimed to assess the effect of TI on sperm activity. Moreover, TI could suppressed the bovine sec

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Luo, Ching-Wei, and 羅清維. "Structure and Function of SVS VII Secreted from Mouse Seminal Vesicle." Thesis, 2000. http://ndltd.ncl.edu.tw/handle/49316805019095828141.

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博士<br>國立臺灣大學<br>生化科學研究所<br>89<br>Mouse seminal vesicle secretion contains seven well-defined major proteins designated SVS I-VII in decreasing order of molecular weight. We used various proteases to carry out proteolysis of the protein components of mouse SVS after their resolution in SDS/PAGE copolymerized with gelatin. Only SVS VII was detected in the gel. SVS VII was purified to homogeneity by chromatography and its antiserum was prepared. The primary structure was established using cDNA cloning and confirmed by protein sequencing. Accordingly, it has a theoretical molecular mass of 8538, w

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Yan-hwa, Lin, and 林彥輝. "Biochemical Study of a Trypsin Inhibitor from Mouse Seminal Vesicle Secretion." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/03456896046561484169.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>82<br>A Kazal-type trypsin inhibitor from mouse seminal vesicle se- cretion was purified to homogeneity via a series of purification steps including ammonium sulfate fractionation, gel filtration, and HPLC on a reverse phase C4 column.The molecular weight of the protein was determined to be 7 kDa by both gel chromatography and SDS PAGE.The protein contained no carbohydrate. Results of direct amino acid sequence determination indicated this protein was the product

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46

Yang, Yun-Hsin, and 楊允馨. "Preliminary study of the gene structure of mouse seminal vesicle autoantigen." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/14603954992729095722.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>82<br>From the analysis of a genomic clone screened from mouse DNA Library, 1016-bp of SVA gene was established. They covered the first exon (122bp), part of the first intron(172bp) and the upstream 722bp from transcriptional start site. Sequence analysis revealed two putative AREs as follows:one between position -124 and -110 (element A, EA) and the other between -213 and -199 (element B, EB)。 EA (AGAACAaagAGTGTG) and EB( AGAACAttcTAATCT) have 66.7% and 83.3% seq

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47

Lai, Min-Long, and 賴明龍. "Biochemical study of a kazal type trypsin inhibitor from mouse seminal vesicle secretion." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/03063349080939818375.

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博士<br>國立臺灣大學<br>生化科學研究所<br>81<br>A Kazal-type trypsin inhibitor purified from mouse seminal vesicle secretion. It was shown to be a weak basic protein with an isoelectric point of 8.7 and it contained no carbohydrate. The protein had a specific activity of 184 U/ miligram protein. Analysis of the kinetic data revealed that the protein was a competitive inhibitor with an inhibitory constant (Ki) of 0.15 nana Mol. The molcular mass of the protein was determined to be 7000. Results of direc

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48

Huang, Hsiu-Ni, and 黃岫妮. "Biochemical Characterization of the Mouse Seminal Vesicle Secretion Sulfhydryl Oxidase -2（SOx-2）." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/81946113468584089103.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>91<br>Sulfhydryl Oxidase-2, SOx-2, is a 66kDa, FAD-binding , monomeric protein. It catalyzes protein disulfide bridge formation and helps unfolded proteins to be matured and biologically functional. From previous studies, SOx is expressed ubiquitously, but most strongly in secretory tissues, such as seminal vesicle, skin apocrine glands and so on.（Colin Thorpe et al.,2002）. In this thesis, we purified SOx-2 protein from mouse seminal vesicle fluid and produced anti-SOx-2 anti-serum. Tissue distributions survey of SOx-2 mRNA showed SOx-2 mRNA is expressed e

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林玲宜. "Biochemical study of a recombinant kazal type trypsin inhibitor from mouse seminal vesicle secretion." Thesis, 1993. http://ndltd.ncl.edu.tw/handle/86086194063145120339.

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Lee, Chin-Mei, and 李金美. "Genetic and Functional Study of the Rat Seminal Vesicle Secretion Protein III, RSVS III." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/24250274396889114322.

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碩士<br>國立臺灣大學<br>生化科學研究所<br>92<br>Rat seminal vesicle secretion protein contains five well-defined major components designated RSVS I-V in decreasing order of molecular weight. RSVS I-III were covalent cross-linked to form high molecular complexes by transglutaminase. RSVS III was confirmed to be derived from RpSV-1 mRNA. RSVS III was immunolocalized in the luminal epithelium of seminal vesicle and the copulatory plug. The genomic structure of RpSv-1(RSVS IIIα)was analyzed to establish a 5’-flanking region of 1771 bp, three exons of 92, 1482 and 327 bp, and two int

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