推荐产品
生物来源
mouse
质量水平
抗体形式
ascites fluid
克隆
3.91D, monoclonal
种属反应性
human
制造商/商品名称
Chemicon®
技术
ELISA: suitable
immunofluorescence: suitable
immunohistochemistry: suitable
western blot: suitable
同位素/亚型
IgG3
运输
wet ice
特异性
Specific for the major envelope protein E of West Nile/Kunjin virus. Kunjin (KUN) is very closely related to some strains of West Nile virus, and has been classified as a subtype of West Nile.
免疫原
Epitope: Envelope
应用
Anti-West Nile Virus/Kunjin Antibody, Envelope, clone 3.91D is an antibody against West Nile Virus/Kunjin for use in ELISA, IF, WB, IH.
外形
Ascites with 0.1% Sodium Azide.
储存及稳定性
Store at -20°C in undiluted aliquots. May be stored at 2-8°C for short term use.
Avoid repeated freeze thaw cycles.
Avoid repeated freeze thaw cycles.
其他说明
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
法律信息
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
10 - Combustible liquids
WGK
nwg
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Characterization of West Nile viruses isolated from captive American Flamingoes (Phoenicopterus ruber) in Medellin, Colombia.
The American Journal of Tropical Medicine and Hygiene null
A PCR-based protocol for the generation of a recombinant West Nile virus.
Virus Research null
Methods in molecular biology (Clifton, N.J.), 1435, 115-127 (2016-05-18)
The West Nile virus (WNV) infection is a major medical problem for humans and some domesticated animals. WNV infection of host cells involves the interplay of the virus with several host factors. Identification of the host factors impacting on WNV
iScience, 27(4), 109539-109539 (2024-05-08)
Rab27a, a Rab family small GTPases, plays an important role in the trafficking and secretion of the intracellular proteins and has been reported to promote various viral multiplication. However, whether Rab27a is involved in West Nile virus (WNV) multiplication is
The American journal of tropical medicine and hygiene, 95(5), 1185-1191 (2016-11-04)
The purpose of this study was to determine the in vitro and ex vivo susceptibility of human corneal cells to West Nile virus (WNV) infection and evaluate the ability of the virus to disseminate to the corneas of infected mice.
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