推荐产品
产品名称
葡聚糖凝胶 ® G-50, Medium
质量水平
表单
slurry
技术
LPLC: suitable
基质
Agarose
基质活性基团
polymer
溶胀
-1 g swells to 9-11 mL
珠子尺寸
50-150 μm
分离技术
size exclusion (SEC)
SMILES字符串
O1C(C(C(C(C1CO)O)O)O)OCC2OC(C(C(C2O)O)O)OCC(O)C(O)C(O)C(O)C=O
InChI
1S/C18H32O16/c19-1-5(21)9(23)10(24)6(22)3-31-17-16(30)14(28)12(26)8(34-17)4-32-18-15(29)13(27)11(25)7(2-20)33-18/h1,5-18,20-30H,2-4H2
InChI key
FZWBNHMXJMCXLU-UHFFFAOYSA-N
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应用
交联葡聚糖凝胶® G-50 是一种用于亲和层析、蛋白质色谱和凝胶过滤色谱的凝胶过滤介质。
分馏范围(MW)
球状蛋白:1,500 - 30,000
右旋糖酐:500-10,000
分馏范围(MW)
球状蛋白:1,500 - 30,000
右旋糖酐:500-10,000
其他说明
G50150-100G的更新产品编号为GE17-0043-01
G50150-500G的更新产品编号为GE17-0043-02
G50150-500G的更新产品编号为GE17-0043-02
法律信息
Sephadex is a registered trademark of Cytiva
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Journal of virology, 54(3), 731-738 (1985-06-01)
An immunoassay was used to examine the interaction between a herpes simplex virus protein, ICP8, and various types of DNA. The advantage of this assay is that the protein is not subjected to harsh purification procedures. We characterized the binding
Nucleic acids research, 15(4), 1559-1577 (1987-02-25)
An RNA molecule consisting of the 5' exon and intervening sequence (IVS) of Tetrahymena precursor rRNA was oxidized with sodium periodate to convert the ribose moiety of the 3' terminal guanosine into a dialdehyde form. The modified RNA undergoes a
Molecular and cellular biology, 10(10), 5106-5113 (1990-10-01)
In HeLa cells, RNA polymerase III (pol III)-mediated transcription is severely inhibited by poliovirus infection. This inhibition is due primarily to the reduction in transcriptional activity of the pol III transcription factor TFIIIC in poliovirus-infected cells. However, the specific binding
Supramolecular organization of S12363-liposomes prepared with two different remote loading processes.
Biochimica et Biophysica Acta - Biomembranes, 1788(5), 926-935 (2009)
FEBS letters, 579(10), 2250-2252 (2005-04-07)
Pi binding by the F(1)-ATPase of beef heart mitochondria and of the Escherichia coli plasma membrane (E. coli F(1)) was examined by two methods: the centrifuge column procedure [Penefsky, H.S. (1977) J. Biol. Chem. 252, 2891-2899] and the Paulus pressure
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