Merck
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MAB837

Sigma-Aldrich

抗-乳头瘤病毒抗体,1、6、11、16、18、31,克隆1H8

clone 1H8, Chemicon®, from mouse

别名:
HPV
eCl@ss:
32160702
NACRES:
NA.41

生物来源

mouse

抗体形式

purified antibody

antibody product type

primary antibodies

克隆

1H8, monoclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable
immunohistochemistry: suitable
western blot: suitable

同位素/亚型

IgG

运输

wet ice

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此商品
MAB8679MAB8051MAB8052
antibody form

purified antibody

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

clone

1H8, monoclonal

clone

TVG 261, monoclonal

clone

2/6, monoclonal

clone

20/11, monoclonal

species reactivity

human

species reactivity

human

species reactivity

human

species reactivity

human

manufacturer/tradename

Chemicon®

manufacturer/tradename

Chemicon®

manufacturer/tradename

Chemicon®

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable, immunohistochemistry: suitable, western blot: suitable

technique(s)

ELISA: suitable, western blot: suitable

technique(s)

ELISA: suitable, flow cytometry: suitable, immunofluorescence: suitable, immunohistochemistry: suitable

technique(s)

ELISA: suitable, flow cytometry: suitable, immunofluorescence: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable

特异性

人乳头瘤病毒蛋白 - HPV-1、HPV-6、HPV-11、HPV-16、HPV-18和HPV-31。

免疫原

SDS破坏的牛乳头瘤病毒1型。
表位:1、6、11、16、18、31

应用

免疫组织化学

ELISA

蛋白质印迹法

最佳工作稀释度必须由最终用户确定。
抗乳头瘤病毒抗体,1、6、11、16、18、31,克隆1H8是用于ELISA、WB、IH的抗乳头瘤病毒抗体。
研究子类别
传染病 - 病毒
研究类别
传染病

外形

形式:纯化
液体形式,溶于0.02 M PB 0.25 M NaCl和0.1%叠氮化钠(pH 7.6)中

储存及稳定性

维持在2-8°C。

其他说明

浓度:关于批次特定浓度请参见检验报告。

法律信息

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

除非我们的目录或产品随附的其他公司文件中另有说明,否则我们的产品预期仅用于研究用途,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或对人类或动物的任何类型的消费或应用。

储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(F)

Not applicable

闪点(C)

Not applicable


Certificates of Analysis (COA)

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Determinants of autoantibody induction by conjugated papillomavirus virus-like particles.
Bryce Chackerian, Petra Lenz, Douglas R Lowy, John T Schiller
Journal of immunology (Baltimore, Md. : 1950) (1950)
Neutralization of bovine papillomavirus by antibodies to L1 and L2 capsid proteins
Roden, R B, et al
Journal of virology, 68, 7570-7574 (1994)
Anna Yemelyanova et al.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 26(2), 268-274 (2012-09-22)
While cervical cancer screening relies on cervical cytology and high-risk human papillomavirus (HPV) detection, the histologic diagnosis, and specifically lesion grade, is the main parameter that drives clinical management of screen-positive women. Morphologically diagnosed squamous intraepithelial lesions (SIL/CIN) regress spontaneously
A A McBride et al.
Proceedings of the National Academy of Sciences of the United States of America, 97(10), 5534-5539 (2000-05-11)
Bovine papillomavirus type 1 (BPV-1) induces fibropapillomas in its natural host and can transform fibroblasts in culture. The viral genome is maintained as an episome within fibroblasts, which has allowed extensive genetic analyses of the viral functions required for DNA
L M Cowsert et al.
Journal of the National Cancer Institute, 79(5), 1053-1057 (1987-11-01)
Monoclonal antibodies (MAbs) were generated against sodium dodecyl sulfate-disrupted bovine papillomavirus type 1 (BPV-1). When screened by enzyme-linked immunosorbent assay (ELISA) on intact and disrupted BPV-1, -2, and deer papillomavirus, three patterns of reactivity were defined: reactivity only with intact

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