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Merck

90358

Triethylammonium acetate buffer

volatile buffer, ~1.0 M in H2O

동의어(들):

Triethylammonium acetate buffer, Buffer solution 1 M pH 7.0 (volatile)

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제품정보 (DICE 배송 시 비용 별도)

UNSPSC Code:
12161700
PubChem Substance ID:
NACRES:
NA.25
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도움 문의

Quality Level

assay

0.95—1.05 mol

form

liquid

shelf life

limited shelf life, expiry date on the label

storage condition

dry at room temperature

concentration

1 M, ~1.0 M in H2O

technique(s)

electrophoresis: suitable

color

colorless

refractive index

n20/D 1.357

pH

7.0

 

6.1

density

1.002 g/mL at 20 °C

suitability

suitable for chromatography, suitable for protein modification, suitable for separation of small nucleic acid fragments

application(s)

detection
diagnostic assay manufacturing
life science and biopharma
sample preparation

storage temp.

2-8°C

InChI

1S/C6H15N.C2H4O2/c1-4-7(5-2)6-3;1-2(3)4/h4-6H2,1-3H3;1H3,(H,3,4)

InChI key

AVBGNFCMKJOFIN-UHFFFAOYSA-N

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General description

Triethylammonium acetate, also known as TEAA, is a volatile buffer widely utilized as a buffer in various biochemical and biological applications, particularly in peptide and proteomics research. It is a common choice for ion-pairing reagent in the chromatographic separation of oligonucleotides and plays a key role in buffer solutions for oligonucleotide synthesis and purification.

Application

Triethylammonium acetate has been used:
  • as a buffer in proteomics studies
  • as a component of the mobile phase to separate nucleotide sugars
  • as a buffer for the separation of glycopeptides in proteomics research

Features and Benefits

  • Suitable for Biological and Biochemical Research
  • Ready available solution reduce the need for preparation time

Other Notes

For additional information on our range of Biochemicals, please complete this form.

저장 등급

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Mapping the O-glycoproteome using site-specific extraction of O-linked glycopeptides (EXoO)
Yang W et al.
Molecular Systems Biology, 14, e8486-e8486 (2018)
Sialic acid biosynthesis pathway blockade disturbs neuronal network formation in human iPSC-derived excitatory neurons
Mijdam R et al.
Journal of Neurochemistry, 167, 76-89 (2023)
Single-molecule mRNA detection and counting in mammalian tissue
Lyubimova A, et al.
Nature Protocols, 8(9) (2013)
Weiming Yang et al.
Nature protocols, 15(8), 2589-2610 (2020-07-19)
Protein glycosylation is one of the most common protein modifications. A major type of protein glycosylation is O-GalNAcylation, in which GalNAc-type glycans are attached to protein Ser or Thr residues via an O-linked glycosidic bond. O-GalNAcylation is thought to play
Johannes Zander et al.
Infection and immunity, 76(4), 1333-1339 (2007-12-28)
Thymidine-dependent small-colony variants (SCVs) of Staphylococcus aureus are frequently associated with persistent and recurrent infections in cystic fibrosis patients. The phenotypic appearance of S. aureus SCVs or normal-colony variants (NCVs) is postulated to be affected by the intracellular amount of

문서

Chromolith® RP-18e columns optimize Oligo Standard 6 separation with varied flow rates and ion-pairing reagent evaluation.

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SKUGTIN
9035804053252734106

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