T1503
Trizma® base
≥99.9% (titration), crystalline, primary standard, aminopeptidase substrate
Synonim(y):
2-Amino-2-(hydroxymethyl)-1,3-propanediol, THAM, Tris base, Tris(hydroxymethyl)aminomethane, Trometamol
About This Item
Polecane produkty
product name
Trizma® base, Primary Standard and Buffer, ≥99.9% (titration), crystalline
Poziom jakości
opis
aminopeptidase substrate
Próba
≥99.9% (titration)
Postać
crystalline
warunki przechowywania
dry at room temperature
metody
ELISA: suitable
protein extraction: suitable
kolor
white
pH
10.5-12
przydatny zakres pH
7-9
pKa (25°C)
8.1
tw
219-220 °C/10 mmHg (lit.)
mp
167-172 °C (lit.)
rozpuszczalność
methanol: soluble 26 mg/mL at 25 °C
ethylene glycol: soluble 79.1 mg/mL at 25 °C
water: soluble (678 g/l at 20 °C)
absorpcja
≤0.05 at 290 nm at 40%
przydatność
suitable for Western blot
suitable for electrophoresis
Zastosowanie
cell analysis
diagnostic assay manufacturing
life science and biopharma
ciąg SMILES
NC(CO)(CO)CO
InChI
1S/C4H11NO3/c5-4(1-6,2-7)3-8/h6-8H,1-3,5H2
Klucz InChI
LENZDBCJOHFCAS-UHFFFAOYSA-N
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Opis ogólny
Tris base may find application as basimetric standard, independently as a buffer and as a crucial component in mixed buffer formulations, including Tris-EDTA (TE) buffer, TAE buffer, TBE buffer, among others. Its attributes include purity, essential stability, and a relative non-hygroscopic nature, making it a dependable choice in laboratory settings. In these environments, Tris base is indispensable for preparing buffers compatible with biological fluids and serves as a standard pH solution. It facilitates various laboratory procedures such as lactate dehydrogenase assays, in situ hybridization, and protein extraction from cells. The versatility of Tris base extends to cell biology, biochemistry, and protein research contributing significantly to studies involving cell membrane permeability and buffer preparation.
Zastosowanie
- as a component of H buffer (cell dissociation buffer)
- for washing and saturation of wells in double sandwich ELISA immunoenzymatic technique
- as an assay buffer for reconstitution of extracted and dried protein samples
- to prepare Tris-HCl buffer that is used to stabilize proteins
- as a buffer to extract carotenoid from tubers
- as a component of sample buffer during protein extraction prior to western blotting
- as a component of sample buffer for sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE)
- to prepare simulated body fluid (SBF) for calcium phosphate (CaP) resorption assay
- as a buffer for polydopamine (PDA) deposition on stainless steel (SS) substrate
Cechy i korzyści
- Efficient buffering within the pH range of 7 - 9 with a pKa of 8.1 (25 °C)
- Tested to confirm low levels of heavy metal contamination, ensuring suitability for various applications
- Can be used in Cell Biology, and Biochemical research
Inne uwagi
For precise applications, use a carefully calibrated pH meter with a glass/calomel combination electrode.
Informacje prawne
najczęściej kupowane z tym produktem
produkt podobny
zalecane rękawice chroniące przed rozpryskami
Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 1
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
dust mask type N95 (US), Eyeshields, Gloves
Certyfikaty analizy (CoA)
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Protokoły
To measure achromopeptidase activity, this procedure uses bacterial cells and a turbidimetric rate assay. Turbidity is measured at 600 nm using a spectrophotometer.
Carboxypeptidase A activity measured via continuous spectrophotometric rate determination assay with hippuryl-L-phenylalanine substrate.
To measure chloramphenicol acetyltransferase activity, this procedure uses DTNB and coenzyme A. The reaction of DTNB with the –SH group on CoA results in a colorimetric increase at 412 nm.
Measure luciferase activity using a luminometer assay detecting light emission, with applications in ATP detection and genetic function reporting.
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