Anti-Proteus spp抗体[31-17]
小鼠单克隆抗体[31-17] to Proteus spp
Mouse
This antibody reacts with approximately 50% of the Proteus spp. isolates tested
适用于: ICC/IFmore details
与反应: Proteus
This antibody reacts with bacteria in suspension and is therefore useful for detection of Proteus spp. in bacterial suspensions. Various systems can be used with this antibody to detect the presence of Proteus spp.
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
Liquid
Shipped at 4°C. Store at +4°C.
pH: 7.3
Preservative: 0.1% Sodium azide
Constituent: 1% BSA
Tissue culture supernatant
This product is sterile filtered.
This antibody reacts with bacteria in suspension and is therefore useful for detection of Proteus spp. in bacterial suspensions. Various systems can be used with this antibody to detect the presence of Proteus spp.
单克隆
31-17
IgG2a
unknown
Abpromise™承诺保证使用ab8469于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度；实际最佳的稀释度/浓度应由使用者检定。
| 应用 | Ab评论 | 说明 |
|---|---|---|
| ICC/IF | Use at an assay dependent concentration. Detection by luminescence, polymerase chain reaction or culture. Magnisort-M particles (DuPont) are diluted 25 times in PBS (+ 1% gelatin). 50 µl is transferred into a microtiterplate well. Add 50-75 µl antibody solution, incubate shaking 15 min. at room temperature. Magnetize plate and remove supernatant. Add 75 µl bacteria suspension and incubate shaking 15 min. at room temperature. Magnetize plate and wash beads three times with PBS-gelatin. Resuspend beads in appropriate volume and prepare for specific detection. Read More |
抱歉，暂无浏览记录
