Bundibugyo Ebolavirus GP 抗体
The HEK-293 Cells 单克隆 anti-Bundibugyo Ebolavirus GP antibody is suitable to detect Bundibugyo Ebolavirus GP in samples from Bundibugyo Virus (BDBV). It has been validated for ELISA, BP, Func, IEM 和 Neut.
产品编号 ABIN7794765
发货至:
中国
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Quick Overview for Bundibugyo Ebolavirus GP 抗体 (ABIN7794765)
抗原
Bundibugyo Ebolavirus GP
适用
Bundibugyo Virus (BDBV)
宿主
HEK-293 Cells
克隆类型
单克隆
标记
非结合性
应用范围
ELISA, Blocking Peptide (BP), Functional Studies (Func), Immunoelectron Microscopy (IEM), Neutralization (Neut)
克隆位点
BDBV-255
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原理
- Anti-Bundibugyo Ebolavirus, GP (Clone BDBV-255)-Purified No Carrier Protein
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特异性
- BDBV-255 activity is directed against an epitope near the base of Bundibugyo ebolavirus (BDBV) glycoprotein. Antigen Distribution Ebola virus glycoprotein is a surface protein expressed on the virus envelope. Background Ebola virus is a member of the Filoviridae family that causes severe disease in humans with a mortality rate of 25-90 % 1. Three Ebola species are responsible for lethal outbreaks Zaire ebolavirus (EBOV), Bundibugyo ebolavirus (BDBV), and Sudan ebolavirus (SUDV). The Ebola virus envelope contains a single surface glycoprotein (GP) which is responsible for viral attachment to the host cell, endosomal entry, and membrane fusion1. GP is composed of two subunits, GP1 and GP2. GP1 has a heavily glycosylated mucin-like domain and a glycan cap. GP2 contains the internal fusion loop, transmembrane domain, and stalk. GP is the major target of neutralizing monoclonal antibody (mAb) and vaccine design against Ebola virus. mAbs targeting GP1 are capable of neutralizing all known filovirus GPs2,3. A pan-Ebola virus mAb is highly desirable to protect against future outbreaks. BDBV-255 is a GP mAb isolated from B cells of a survivor of the 2007 Uganda BDBV outbreak3. Peripheral blood mononuclear cells from the survivor were transformed with Epstein-Barr virus, CpG, and additional supplements. Subsequently, cell supernatants were screened by ELISA for binding to GPs from BDBV, EBOV, or MARV filoviruses. Positive cells were fused with HMMA2.5 myeloma cells by electrofusion and cloned by single-cell fluorescence-activated cell sorting. In binding and neutralization assays, BDBV-255 binds to and neutralizes BDBV but not other filoviruses3. BDBV-255 targets an epitope that extends below the base of GP, possibly within the membrane-proximal external region (MPER) of GP2, in a region that is likely not conserved between filoviruses. Stable binding may require the full MPER, transmembrane domain regions, and a membrane. One GP trimer is able to accommodate three BDBV-255 antibodies.
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纯化方法
- Recombinant antibodies are manufactured in an animal free facility using only in vitro protein free cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates.
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纯度
- >=90 % monomer by analytical SEC and SDS-Page
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亚型
- IgG1 lambda
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限制
- 仅限研究用
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浓度
- 1 μg/mL
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缓冲液
- This recombinant monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration.
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储存液
- Without preservative
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储存条件
- 4 °C,-80 °C
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储存方法
- This antibody may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at <= -70°C.Avoid Repeated Freeze Thaw Cycles.
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- Bundibugyo Ebolavirus GP
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物质类
- Viral Protein
抗原
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