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皰疹病毒2IgM(HSV 2-IgM)
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意大利進(jìn)口TORCH試劑

測(cè)IgM為較受推崇的抗體捕獲法,測(cè)IgG為6點(diǎn)定標(biāo)的定量間接法,總準(zhǔn)確率可達(dá)到98~100%

不同品種操作完全一致,已稀釋樣本可多項(xiàng)檢測(cè)

樣本溫育只需45分鐘(在同類產(chǎn)品中時(shí)間最短)

全部操作流程只需2~3小時(shí)(取決于樣本量),即使開(kāi)展全部8項(xiàng)檢測(cè)亦可在半個(gè)工作日內(nèi)輕松完成

底物為單一底物液,簡(jiǎn)化操作,減少誤差

稀釋液、洗滌液、底物液、終止液均可通用

試劑及包裝均有顏色標(biāo)記,減少操作失誤

單純皰疹病毒2型IgM抗體HSV 2-IgM

酶聯(lián)免疫吸附測(cè)定法(ELISA)試劑盒

捕獲法



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用途

?單純皰疹病毒2型IgM抗體HSV 2-IgM酶聯(lián)免疫吸附測(cè)定法(ELISA)試劑盒用于體外半定量檢測(cè)人血清中的HSV 2 IgM抗體,并輔助診斷皰疹相關(guān)性疾病。高度復(fù)雜的檢測(cè)。



1.?????? 引言

在全世界范圍內(nèi)都存在人類的單純皰疹病毒(HSV)感染。HSV感染的臨床病程差異很大,而大多數(shù)病例為癥狀輕微的隱性感染(通常不能察覺(jué))。臨床征象明顯的HSV感染表現(xiàn)不一,既可為輕微的咽炎,又可為致死性的嚴(yán)重泛發(fā)性疾病。與HSV感染有關(guān)的主要臨床疾病為齦口炎、角膜炎、結(jié)膜炎、皮膚皰疹、無(wú)菌性腦膜炎、腦炎、生殖道感染以及新生兒皰疹。新生兒感染可局限在皮膚,或者泛發(fā),嚴(yán)重累及中樞神經(jīng)系統(tǒng)、眼、皮膚以及其他器官。

單純皰疹病毒有兩種類型,它們?cè)谛螒B(tài)學(xué)上無(wú)法區(qū)分,而且約40%的DNA堿基序列相同,有許多共同抗原,可產(chǎn)生相同的皮膚和粘膜病變??赏ㄟ^(guò)其抗原、生物學(xué)、生物化學(xué)以及臨床和流行病學(xué)行為的差別來(lái)區(qū)分這兩種類型的病毒。HSV 2通過(guò)性傳播,或由母親的生殖器感染傳遞給新生兒。它可導(dǎo)致大多數(shù)生殖器皰疹、新生兒皰疹以及腰部以下的皮膚感染。HSV 1主要通過(guò)非性途徑來(lái)傳播,通常是由于接觸了感染者的唾液而受到傳染。除新生兒皰疹之外,兒童時(shí)期的大多數(shù)HSV感染均是由HSV 1引致的。性行為是HSV 2感染傳播的途徑,因此在開(kāi)始性行為之前,很少發(fā)生HSV 2感染(1,2,3,4,5,6)。

大多數(shù)人在20歲之前就已感染過(guò)HSV(7,8)。因此,任何血清學(xué)方法檢測(cè)到的血清中抗HSV抗體均不能提示感染的時(shí)間,除非進(jìn)行特異性IgM抗體檢測(cè)。HSV初次感染之后,抗體水平逐漸下降至較低或檢測(cè)不到的水平,以后如果發(fā)生同一類型或不同類型的臨床感染,抗體會(huì)受到刺激而再次抬升。

初次感染是針對(duì)以前未感染過(guò)HSV 1或HSV 2的個(gè)體而言。已經(jīng)知道,過(guò)去感染過(guò)HSV 1并不能保護(hù)該個(gè)體不會(huì)受到HSV 2的感染;然而,如果以前曾感染過(guò)HSV 1,而后又發(fā)生了HSV 2感染,這類患者的臨床表現(xiàn)會(huì)有所減輕(7)。



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2.?????? 參考文獻(xiàn)

1. Oxman, M.N., D.D. Richman & S.A. Spector. 1982. Management at delivery of mother and infant when herpes simplex, varicella zoster, hepatitis, or tuberculosis have occurred during

pregnancy. In: Current Clinical Topics in Infectious Diseases: pp 224-280

2. Nahmias, A.J., & W.E. Josey. 1982. Herpes simplex viruses 1 and 2. In: Viral Infections of Humans, Evans, A.S. ed. 2 nd Edition. New York: Plenum Press: p 351

3. Centers for Disease Control. Genital herpes infection - United States, 1966-1979. 1982. Morbid Mortal. Wkly Rep. 31:11.

4. Gardner, H.I. 1979. Herpes genitalis: Our most important venereal disease. Am. J. Obstet. Gynecol. 135: 553

5. Bolognese, R.J., et al. 1976. Herpesvirus hominis type II infections in asymptomatic pregnant women. Obstet. Gynecol. 48: 507

6. Sumaya, C.V., et al. 1980. Genital infections with herpes simplex virus in a university student population. Sex Trans. Dis. 7:16

7. Stewart, J.A., & K.L. Herrmann. 1986. Herpes Simplex Virus. In: Manual of Clinical Laboratory Immunology. Rose, N.R., Friedman, H., Fahey, J.L., eds. 3rd Edition. Wash, D.C. ASM. pp 497-501.

8. Rawls, W.E., & J. Campione-Piccardo. 1981. Epidemiology of herpes simplex virus type 1 and 2 infections. In: The human herpesviruses: an interdisciplinary perspective. Nahmias, A.J., Dowdle, W.R., and Schinazi, R.F., eds. New York: Elsevier: pp137-152.

9.National Committee for Clinical Laboratory Standards. 1990. Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture Approved Standard. NCCLS Publication H18-A.

10. NCCLS. 1991. National Committee for Clinical Laboratory Standard. Internal Quality Control Testing: Principles & Definition. NCCLS Publication C24- A.

11. Engvall, E., K. Jonsson, and P. Perlman. 1971. Enzyme-Linked Immunosorbent Assay, (ELISA) Quantitative Assay of Immunoglobulin G. Immunochemistry. 8:871-874.

12. Engvall, E. and P. Perlman. 1971. Enzyme-Linked Immunosorbent Assay, ELISA. In: Protides of the Biological Fluids. H. Peeters, ed. Proceedings of the Nineteenth Colloquium, Brugge Oxford. Pergamon Press. pp 553-556.

13. Engvall, E., K. Jonsson, and P. Perlman. 1971. Enzyme-Linked Immunosorbent Assay. II. Quantitative Assay of Protein Antigen, Immunoglobulin-G, By Means of Enzyme- Labelled Antigen and Antibody-Coated tubes. Biochem. Biophys. Acta. 251: 427- 434.

14. Van Weeman, B. K. and A.H.W.M. Schuurs. 1971. Immunoassay Using Antigen-Enzyme Conjugates. FEBS Letter. 15:232-235.

15. CDC/NIH Interagency Working Group. 1993. Biosafety in Microbiological and Biomedical Laboratories. 3rd Edition. U. S. Dept. of Health and Human Services, Public Health Service. pp18-24.

16. http://www.cap.org/html/ftpdirectory/checklistftp.html. 1998. Laboratory General - CAP (College of American Pathology) Checklist (April 1998). pp 28-32.

17. NCCLS. 1997. National Committee for Clinical Laboratory Standard. Preparation and Testing of Reagent Water in the Clinical Laboratory. NCCLS Publication C3- A3.


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