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SYNC384640C

Synthware chromatography column with reservoir, fritted disc and PTFE stopcock

500 mL, joint: ST/NS 35/20, I.D. × L 40.0 mm × 457 mm

Synonym(s):

Synthware C384640C, glass chromatograpy column

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25 G
CN¥1,541.64
100 G
CN¥4,201.18

CN¥1,541.64


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25 G
CN¥1,541.64
100 G
CN¥4,201.18

About This Item

UNSPSC Code:
23151816
NACRES:
NB.51

CN¥1,541.64


In StockDetails


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Joint

joint: ST/NS35/20

packaging

pkg of 1 ea

manufacturer/tradename

Synthware C384640C

technique(s)

HPLC: suitable

I.D. × L

40.0 mm × 457 mm

capacity

500 mL

suitability

suitable for chromatography

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This Item
T12589334893328
assay

≥99.0% (NT)

assay

≥99.0% (titration)

assay

≥99.0% (NT)

assay

≥99.5% (NT)

product line

BioUltra

product line

-

product line

BioXtra

product line

BioUltra

Quality Level

300

Quality Level

300

Quality Level

200

Quality Level

100

form

crystalline powder

form

crystalline powder

form

crystalline powder

form

powder or crystals

solubility

H2O: 0.5 M at 20 °C, clear, colorless

solubility

water: 0.5 M, clear, colorless

solubility

H2O: 0.5 M at 20 °C, clear

solubility

H2O: 0.5 M at 20 °C, clear, colorless

pH

6.0-7.0 (25 °C, 0.5 M in H2O)

pH

6.0-7.0 (0.1 M in water, high purity)

pH

-

pH

3.0-4.5 (25 °C, 0.5 M in H2O)

General description

With a coarse porosity fritted disc to support packing ,with 35/20 spherical joint. All Synthware columns are heavy wall designed to increase safety.

Legal Information

Synthware is a trademark of Kemtech America Inc.

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M Ito et al.
Life sciences, 38(12), 1089-1096 (1986-03-24)
[3H]L-glutamic acid binding to microfuge tubes and glass was investigated in four buffers. Background binding to these materials was negligible, but was increased by centrifugation or suction in Tris-HCl and Tris-citrate buffer. This binding was much less or eliminated when
Chi-Lin Li et al.
The Analyst, 137(22), 5222-5228 (2012-10-04)
Oligonucleotide (T30695) modified gold nanoparticles (T30695-Au NPs) have been prepared and employed for quantification of lead ions (Pb(2+)) in blood. The detection of Pb(2+) ions is through the formation of Au-Pb alloys and oligonucleotide-Pb(2+) complexes that catalyze the H(2)O(2)-mediated oxidation
Monica Cubillos-Rojas et al.
Methods in molecular biology (Clifton, N.J.), 869, 205-213 (2012-05-16)
Polyacrylamide gel electrophoresis (PAGE) is one of the most powerful tools used for protein analysis. We describe the use of Tris-acetate buffer and 3-15% polyacrylamide gradient gels to simultaneously separate proteins in the mass range of 10-500 kDa. We show
Patrick S Aranda et al.
Electrophoresis, 33(2), 366-369 (2012-01-10)
RNA-based applications requiring high-quality, non-degraded RNA are a foundational element of many research studies. As such, it is paramount that the integrity of experimental RNA is validated prior to cDNA synthesis or other downstream applications. In the absence of expensive
Monica Cubillos-Rojas et al.
Electrophoresis, 31(8), 1318-1321 (2010-03-24)
To separate and analyze giant and small proteins in the same electrophoresis gel, we have used a 3-15% polyacrylamide gradient gel containing 2.6% of the crosslinker bisacrylamide and 0.2 M of Tris-acetate buffer (pH 7.0). Samples were prepared in a

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