추천 제품
제품명
Sephadex® G-50, Medium
Quality Level
양식
slurry
기술
LPLC: suitable
Matrix
Agarose
기질 활성군
polymer
팽창
-1 g swells to 9-11 mL
비드 크기
50-150 μm
분리 기술
size exclusion (SEC)
SMILES string
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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애플리케이션
Sephadex® G-50 is a gel filtration medium used in affinity chromatography, protein chromatrography and gel filtration chromatography.
Fractionation Range (MW)
Globular Proteins: 1,500 - 30,000
Dextrans: 500 - 10,000
Fractionation Range (MW)
Globular Proteins: 1,500 - 30,000
Dextrans: 500 - 10,000
기타 정보
G50150-100G′s updated product number is GE17-0043-01
G50150-500G′s updated product number is GE17-0043-02
G50150-500G′s updated product number is GE17-0043-02
법적 정보
Sephadex is a registered trademark of Cytiva
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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시험 성적서(COA)
Lot/Batch Number
M E Clark et al.
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.
Chemin, C., et al.
Biochimica et Biophysica Acta - Biomembranes, 1788(5), 926-935 (2009)
P S Kay et al.
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
C K Lee et al.
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
Harvey S Penefsky
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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