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574793

Sigma-Aldrich

TE Buffer, 100X, Molecular Biology Grade

A 100X concentrate that, when diluted to 1X, contains 10 mM Tris, 1 mM EDTA, pH ~8.0.

Synonym(s):

Tris-EDTA Buffer

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About This Item

UNSPSC Code:
41105319
NACRES:
NA.25
Pricing and availability is not currently available.
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grade

Molecular Biology

form

liquid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated

foreign activity

DNase, RNase, protease, none detected

shipped in

ambient

storage temp.

15-25°C

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This Item
C5132
Carbazole ≥95% (GC)

C5132

Carbazole

assay

95%

assay

≥95% (GC)

Quality Level

100

Quality Level

200

mp

78-82 °C (lit.)

mp

243-246 °C (lit.)

functional group

hydroxyl

functional group

-

General description

A 100X concentrate that, when diluted to 1X, contains 10 mM Tris, 1 mM EDTA, pH ~8.0.
Tris-ethylenediaminetetraacetic (TE) buffer is a common buffer used in molecular biology to maintain the integrity of nucleic acid during handling and storage.[1]

Application

TE Buffer, 100X, Molecular Biology Grade – Calbiochem has been used to dilute DNA stock solutions.[2] It has also been used to dilute thymidylate synthase (thyA) culture for colony polymerase chain reaction (PCR).[3]

Warning

Toxicity: Irritant (B)

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1


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Thermal aging of single-layer polymer light-emitting diodes composed of a carbazole and oxadiazole containing copolymer doped with singlet or triplet emitters.
Rungta P, et al.
Synthetic Metals, 160(23), 2486-2493 (2010)
Rukiye Ayranci et al.
The Analyst, 142(18), 3407-3415 (2017-08-22)
Herein, we report the synthesis and characterization of a new rhodamine-based monomer (RD-CZ), and an investigation of the optical and electrochemical properties of the corresponding polymer (P(RD-CZ)), which was electropolymerized on an ITO electrode. The resulting P(RD-CZ) polymer film was
Synthesis and photophysical properties of a poly (methyl methacrylate) polymer with carbazolyl side groups.
Martins TD, et al.
Journal of the Brazilian Chemical Society, 19(8), 1450-1461 (2008)
Yifen Lin et al.
Food chemistry, 264, 1-8 (2018-06-02)
Disassembly of cell wall polysaccharides accompanied with softening is very common in harvested fruits. To develop a facile postharvest approach, which can be used at ambient temperature, for suppressing softening and maintaining higher nutritive cell wall polysaccharides of Younai plums
Poly(methyl methacrylate)copolymers containing pendant carbazole and oxadiazole moieties for applications in single-layer organic light emitting devices.
Evanoff DD, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(23), 7882-7897 (2008)

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