نتایج جستجو برای: vp2 protein

تعداد نتایج: 1235227  

Journal: :Journal of virology 1984
W Lin T Hata H Kasamatsu

The amounts of simian virus 40 structural polypeptides Vp1, Vp2, and Vp3 in different subcellular fractions at various times after lytic infection were determined by a quantitative immunoblotting procedure. Simian virus 40-infected cells were lysed with a buffer containing Nonidet P-40 to yield a soluble fraction. The Nonidet P-40-insoluble fraction was further fractionated in the presence of d...

Journal: :Development 2000
J M Brickman C M Jones M Clements J C Smith R S Beddington

One of the earliest markers of anterior asymmetry in vertebrate embryos is the transcription factor Hex. We find that Hex is a transcriptional repressor that can be converted to an activator by fusing full length Hex to two copies of the minimal transcriptional activation domain of VP16 together with the flexible hinge region of the (lambda) repressor (Hex-(lambda)VP2). Retention of the entire ...

Journal: :Journal of clinical microbiology 2007
Dorsaf Nasri Lamjed Bouslama Shabir Omar Henia Saoudin Thomas Bourlet Mahjoub Aouni Bruno Pozzetto Sylvie Pillet

The sequencing of the VP1 hypervariable region of the human enterovirus (HEV) genome has become the reference test for typing field isolates. This study describes a new strategy for typing HEV at the serotype level that uses a reverse transcription-PCR assay targeting the central part of the VP2 capsid protein. Two pairs of primers were used to amplify a fragment of 584 bp (with reference to th...

2013
Omid Taghavian Holger Spiegel Rüdiger Hauck Hafez M. Hafez Rainer Fischer Stefan Schillberg

Infectious bursal disease virus (IBDV) causes economically important immunosuppressive disease in young chickens. The self-assembling capsid protein (VP2) from IBDV strain IR01 was expressed in Pichia pastoris resulting in the formation of homomeric, 23-nm infectious bursal disease subviral particles (IBD-SVPs) with a yield of 76 mg/l before and 38 mg/l after purification. Anti-IBDV antibodies ...

Journal: :The Journal of infectious diseases 2004
Amanda Corcoran Bernard P Mahon Sean Doyle

BACKGROUND Loss of antibody reactivity against linear epitopes of parvovirus B19 (B19) capsid proteins VP1 and VP2 occurs after infection; however, it is unclear whether B cell memory is established against linear epitopes. METHODS B cell enzyme-linked immunospot assay was used to evaluate B19-specific B cell memory in volunteer donors (n=22). RESULTS B cell memory is maintained against con...

پایان نامه :وزارت علوم، تحقیقات و فناوری - پژوهشگاه ملی مهندسی ژنتیک وزیست فناوری 1391

بیماری بورس عفونی در جوجه ها سبب سرکوب سیستم ایمنی جوجه شده و از این طریق عفونت های بعدی ایجاد می گردد. در حال حاضر انواع واکسن های حاصل از تکثیر ویروس برای مقابله با این عفونت استفاده می شود. استفاده از واکسن های زیر واحدی در سال های اخیر مورد توجه قرار گرفته است. آنتی ژن سطحی vp2 بعنوان آنتی ژن هدف جهت تولید واکسن زیر واحدی گزینه مناسبی است. مطالعات متعددی بر روی تولید این پروتئین در سیستم ها...

2017
Pei Zhou Weijie Zeng Xin Zhang Shoujun Li

To trace the evolution process of CPV-2, all of the VP2 gene sequences of CPV-2 and FPV (from 1978 to 2015) from GenBank were analyzed in this study. Then, several new ideas regarding CPV-2 evolution were presented. First, the VP2 amino acid 555 and 375 positions of CPV-2 were first ruled out as a universal mutation site in CPV-2a and amino acid 101 position of FPV feature I or T instead of onl...

Journal: :Clinical and diagnostic laboratory immunology 2005
Fan Li Rachel A Stevenson Brendan S Crabb Michael J Studdert Carol A Hartley

Equine rhinitis A virus (ERAV) is a significant pathogen of horses and is also closely related to Foot-and-mouth disease virus (FMDV). Despite these facts, knowledge of the prevalence and importance of ERAV infections remains limited, largely due to the absence of a simple, robust diagnostic assay. In this study, we compared the antigenicities of recombinant full-length and fragmented ERAV caps...

B. B. Bhanderi, C. G. Joshi C. Hiremath M. K. Jhala

Chicken anemia virus was detected by PCR in tissue samples collected from poultry flocks in Gujarat,India. The VP1, VP2 and VP3 gene sequences of CAV from Anand, Gujarat were obtained after cloning thePCR products in pDrive cloning vector. Nucleotide sequence alignment with other CAV sequencesdemonstrated overall identity of 95-98.8%, 98.8-99.8% and 98.8-100% for VP1, VP2 and VP3 regions,respec...

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