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生物源
mouse
品質等級
共軛
unconjugated
抗體表格
affinity isolated antibody
抗體產品種類
primary antibodies
無性繁殖
GT844, monoclonal
形狀
buffered aqueous solution
分子量
27kDa
濃度
1mg/mL
技術
immunofluorescence: 1:100-1:1,000
western blot: 1:500-1:3,000
同型
IgG2a
運輸包裝
wet ice
儲存溫度
−20°C
目標翻譯後修改
unmodified
一般說明
The acceptor mCherry is a monomeric, red fluorescent protein obtained from the stony-coral Discosoma protein DsRED. It is expressed in the cytoplasm, has a high photostability and is unaffected by photobleaching. mCherry acts as a good FRET (fluorescence resonance energy transfer) acceptor. mCherry allows rapid fluorescence detection after a particular gene is expressed.
免疫原
Full length mCherry recombinant protein
應用
Suggested starting dilutions are as follows: WB: 1:500-1:3000. Not yet tested in other applications. Optimal working dilutions should be determined experimentally by the end user.
特點和優勢
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.
其他說明
Purification: Affinity purified by Protein G
外觀
Phosphate-buffered saline, no preservative added.
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 2
閃點(°F)
Not applicable
閃點(°C)
Not applicable
In vitro screening test using Leishmania promastigotes stably expressing mCherry protein.
Antimicrobial Agents and Chemotherapy, 58(3), 1825-1828 (2014)
Quantitative FRET Analysis With the E0GFP?mCherry Fluorescent Protein Pair.
Photochemistry and Photobiology, 85(1), 287-297 (2009)
Nature neuroscience, 26(3), 458-469 (2023-01-24)
Poor sleep is associated with the risk of developing chronic pain, but how sleep contributes to pain chronicity remains unclear. Here we show that following peripheral nerve injury, cholinergic neurons in the anterior nucleus basalis (aNB) of the basal forebrain
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