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Merck

T9784

Tricine

BioXtra, pH 4.0-6.0 (1 M in H2O), ≥99% (titration)

Sinónimos:

N-[Tris(hydroxymethyl)methyl]glycine

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Fórmula lineal:
(HOCH2)3CNHCH2CO2H
Número CAS:
5704-04-1
Peso molecular:
179.17
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
24900603
EC Number:
227-193-6
Beilstein/REAXYS Number:
1937804
MDL number:
MFCD00004277

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SMILES string

OCC(CO)(CO)NCC(O)=O

InChI key

SEQKRHFRPICQDD-UHFFFAOYSA-N

InChI

1S/C6H13NO5/c8-2-6(3-9,4-10)7-1-5(11)12/h7-10H,1-4H2,(H,11,12)

product line

BioXtra

assay

≥99% (titration)

form

powder

impurities

≤0.005% Phosphorus (P), ≤0.1% Insoluble matter

ign. residue

≤0.1%

pH

4.0-6.0 (1 M in H2O)

useful pH range

7.4-8.8

pKa (25 °C)

8.1

solubility

H2O: 1 M, clear, colorless

anion traces

chloride (Cl-): ≤0.1%, sulfate (SO42-): ≤0.05%

cation traces

Al: ≤0.0005%, Ca: ≤0.0005%, Cu: ≤0.0005%, Fe: ≤0.0005%, K: ≤0.005%, Mg: ≤0.0005%, NH4+: ≤0.05%, Na: ≤0.005%, Pb: ≤0.001%, Zn: ≤0.0005%

absorption

≤0.05 at 280 in H2O at 1 M, ≤0.1 at 260 in H2O at 1 M

application(s)

diagnostic assay manufacturing

Quality Level

400

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General description

The name Tricine is derived from "tris" and "glycine". Tricine and other good buffers serve as efficient scavengers of hydroxyl radicals in a study of radiation-induced membrane damage. Tricine is widely used as an electrophoresis buffer and for the resuspension of cell pellets. Due to its lower negative charge compared to glycine, it migrates faster. It has a high ionic strength which leads to more ion movement and less protein movement. This aids the separation of low molecular weight proteins in lower percent acrylamide gels. Tricine is also used as a trailing ion that permits the resolution of small proteins at lower acrylamide concentrations than in glycine-sodium dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE) systems.

Application

Buffer component for separation of low molecular weight peptides.
Tricine has been used:
  • in a polymerase chain reaction (PCR) buffer used in the single-cell collection
  • as a component of lactotroph feeding medium for culturing lactotrophs
  • to prepare luciferase assay reagent for luciferase activity assay in firefly Photonis pyralis and as a component in Triton/glycylglycine lysis buffer

Clase de almacenamiento

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000521336
0000521335
0000521334
0000521334
0000521336

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Encyclopedia of Dairy Sciences (2011)
Joke Mertens et al.
Bio-protocol, 9(13), e3283-e3283 (2019-07-05)
Detecting heteroplasmies in the mitochondrial DNA (mtDNA) has been a challenge for many years. In the past, Sanger sequencing was the main option to perform this analysis, however, this method could not detect low frequency heteroplasmies. Massive Parallel Sequencing (MPS)
Analysis of gene promoter regulation by tumor suppressor genes.
Kumaravel Somasundaram et al.
Methods in molecular biology (Clifton, N.J.), 223, 101-116 (2003-06-05)
Boštjan Rituper et al.
Nature protocols, 8(6), 1169-1183 (2013-05-25)
In order to understand exocytosis and endocytosis, it is necessary to study these processes directly. An elegant way to do this is by measuring plasma membrane capacitance (C(m)), a parameter proportional to cell surface area, the fluctuations of which are
Thierry Rabilloud
Journal of proteomics, 73(8), 1562-1572 (2010-04-17)
Electrophoretic separations of proteins are widely used in proteomic analyses, and rely heavily on SDS electrophoresis. This mode of separation is almost exclusively used when a single dimension separation is performed, and generally represents the second dimension of two-dimensional separations.
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Product Information Sheet - T9784

Product Information Sheet

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