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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
"-20°C/-80°C"
- 保质期：
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
- 英文名：
Customized Drosophila persimilis flower Protein (in vitro E.coli)
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 规格：
20ug
Alternative Name(s)
Calcium channel flowerEditorial/Sponsord
EditorialUniprot ID
B4GRI8Gene Names
flowerOrganism
Drosophila persimilisAASequence
MSFAEKITGLLARPNQQDPVGGPEQPWYLKYGSRLLGIVAAFFAILFGLWNVLSIITLSV SCLVAGIIQMIAGFIVMVLEAPCCFVCIEQVNGIADKVDAKPMYFRAGLYCALAVPPIFM CFGLASLFGSGLIFATGAVYAMMALGKKASAEDMRAAAQQTGYGGNGTAASTTNDRAGIV NNAQPFSFTGAVGTDSNVExpression Region
1-198aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1506Purity
Greater than 85% as determined by SDS-PAGE.Storage Buffer
Tris/PBS-based buffer, 6% TrehaloseStorage
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.Endotoxin
Not Test. Endotoxin removal service is available for free upon you request.产品类型
Transmembrane-Protein备注
**产品信息可能有变动，请以官网信息为准
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文献和实验**产品信息可能有变动，请以官网信息为准
Claudin Family Proteins in Caenorhabditis elegans
in the greater PMP22/EMP/claudin/calcium channel γ subunit family, including nsy-1-nsy-4 and vab-9 , while highly divergent at a sequence level from each other and from the vertebrate claudins, in some cases play roles similar to those traditionally assigned
- 1 Channel 收集的绿色荧光信号，来自 JC- 1 monomer；纵轴示 FL- 2 Channel 收集的红色荧光信号，来自 JC- 1 aggregates。5. C 图细胞群为正常对照，我把细胞群摆在近中央的位置。D 图是 CCCP 处理过的细胞，相对于对照，可见 CCCP 处理的细胞群往右下方发生移动，即红色荧光减弱，绿色荧光增强，这表明 CCCP 处理导致线粒体膜电位下降。6. 如何定量分析：通过 winMDI 2.9 软件可分别得到 FL- 1 channel 和 FL- 2 Channel
Use of the B.D. FACS or Calibur Flow Cytometers
into another channel. Place a FITC-only positive control sample on the machine. Using a dot plot of FL1 vs FL2 be sure that cells positive for FL1 do not exceed a value of 101 for FL2. Use the minimum amount of compensation of FL2 (FL2 = FL2 - %FL1) to eliminate
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