추천 제품
Quality Level
형태
liquid
농도
~1.0 M in H2O
refractive index
n20/D 1.355
pH
8.4-8.6 (25 °C)
density
1.018 g/mL at 20 °C
λ
neat
UV 흡수
λ: 260 nm Amax: ≤0.05
λ: 280 nm Amax: ≤0.05
응용 분야
diagnostic assay manufacturing
저장 온도
2-8°C
SMILES string
OC(O)=O.CCN(CC)CC
InChI
1S/C6H15N.CH2O3/c1-4-7(5-2)6-3;2-1(3)4/h4-6H2,1-3H3;(H2,2,3,4)
InChI key
AFQIYTIJXGTIEY-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Buffer for use in ion-exchange chromatography and electrophoresis.
기타 정보
For use in ion-exchange chromatography and electrophoresis
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Use of triethlammonium buffers in ion-exchange chromatography and electrophoresis.
J PORATH
Nature, 175(4454), 478-478 (1955-03-12)
Dwayne A Elias et al.
Nucleic acids research, 37(9), 2926-2939 (2009-03-19)
Hypothetical (HyP) and conserved HyP genes account for >30% of sequenced bacterial genomes. For the sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough, 347 of the 3634 genes were annotated as conserved HyP (9.5%) along with 887 HyP genes (24.4%). Given the large
C G Huber et al.
Journal of mass spectrometry : JMS, 35(7), 870-877 (2000-08-10)
The applicability of ion-pair reversed-phase high-performance liquid chromatography/electrospray ionization mass spectrometry (IP-RP-HPLC/ESI-MS) and direct infusion/ESI-MS to the characterization of nucleic acid mixtures was evaluated by the analysis of the reaction products obtained from solid-phase synthesis of a 39-mer oligonucleotide. IP-RP-HPLC/ESI-MS
C W Mahoney et al.
Analytical biochemistry, 138(1), 246-251 (1984-04-01)
The separation of 5'-adenosine di- and triphosphates from inorganic pyrophosphate or imidodiphosphate can be accomplished with reverse-phase HPLC by using a solvent system buffered by triethylammonium bicarbonate (pH 6.7). This buffer was used because it was neutral, readily volatile at
Marco L Hennrich et al.
Analytical chemistry, 81(18), 7814-7822 (2009-08-20)
In proteomics, proteolytic peptides are often chemically modified to improve MS analysis, peptide identification, and/or to enable protein/peptide quantification. It is known that such chemical modifications can alter peptide fragmentation in collision induced dissociation MS/MS. Here, we investigated the fragmentation
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