H4034
HEPES
BioPerformance Certified, ≥99.5% (titration), suitable for cell culture
Synonim(y):
4-(2-Hydroxyethyl)piperazine-1-ethanesulfonic acid, N-(2-Hydroxyethyl)piperazine-N′-(2-ethanesulfonic acid)
About This Item
Polecane produkty
klasa czystości
BioPerformance Certified
Poziom jakości
Próba
≥99.5% (titration)
Postać
crystalline powder
warunki przechowywania
dry at room temperature
metody
cell culture | mammalian: suitable
competitive inhibition ELISA: suitable
zanieczyszczenia
endotoxin and total aerobic microbial count, tested
kolor
white
przydatny zakres pH
6.8-8.2
pKa (25°C)
7.5
ślady kationów
Fe: ≤5 ppm
absorpcja
≤0.05 at 260 in H2O at 0.1 M
≤0.05 at 280 in H2O at 0.1 M
przydatność
suitable for Western blot
suitable for component for culture media
Zastosowanie
clinical research
diagnostic assay manufacturing
general analytical
life science and biopharma
obecność zanieczyszczeń
DNase, RNase, NICKase, protease, none detected
ciąg SMILES
OCCN1CCN(CC1)CCS(O)(=O)=O
InChI
1S/C8H18N2O4S/c11-7-5-9-1-3-10(4-2-9)6-8-15(12,13)14/h11H,1-8H2,(H,12,13,14)
Klucz InChI
JKMHFZQWWAIEOD-UHFFFAOYSA-N
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Opis ogólny
HEPES also proves advantageous in various biological and biochemical processes. Its ampholytic nature makes it suitable as a separator for creating pH gradients in isoelectric focusing, a technique often employed in protein separation and analysis. Moreover, HEPES exhibits minimal interference with DNA-restriction enzyme reactions compared to buffers with fewer substituted amine groups, such as Tris. This makes it a preferred choice for applications involving DNA manipulation and analysis. Beyond these specific applications, HEPES is valuable in numerous other biological and biochemical processes, including immunoprecipitation, cell lysis, and live cell imaging. Its versatility, coupled with exceptional pH buffering capacity and minimal interaction with other molecules, establishes HEPES as an indispensable tool across diverse research domains.
Zastosowanie
- To supplement Dulbecco′s modified Eagle′s medium to culture and maintain cell lines
- As a component of platelet suspension buffer
- To supplement Hank′s basic salt solution, which is used to wash pancreatic tissue
- As a component of wash buffer and blocking buffer in the purification and quantification of protein with enzyme-linked immunosorbent (ELISA) assay
- For the adjustment and maintenance of pH of biological solutions
- As a component of Hank′s balanced salt solution (HBSS) and dissociation medium to study neuronal development
- For homogenization of tissue and in the preparation of cytosolic and nuclear extract from cells
- As a component of keratinocyte and fibroblast culture medium
Cechy i korzyści
- Tested to confirm low levels of heavy metal contamination, ensuring suitability for various applications
- Highly soluble in water with a useful pH range of 6.8 - 8.2 and pKa of 7.5 at 25 °C
- Negligible metal ion binding
- Less toxic to cells than other buffers such as Tris and phosphate
- Stable in a wide pH range
- Tested for Endotoxins and Total Aerobic Microbial Count
- Free from DNase, NICKase, RNase, Endonuclease, Exonuclease and Protease
Inne uwagi
najczęściej kupowane z tym produktem
produkt podobny
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
Eyeshields, Gloves, type N95 (US)
Certyfikaty analizy (CoA)
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Protokoły
This protocol describes a method for chemical cross-linking of proteins using formaldehyde. With the exception of zero-length cross-linkers, formaldehyde has the shortest cross-linking span (~2-3 Å) of any cross-linking reagent, thus making it an ideal tool for detecting specific protein-protein interactions with great confidence.
cAMP measurements are obtained using an ELISA assay (Harlow and Lane 1988). Commercial radio-immunoassays, or ELISA kits, to assay cAMP can be purchased from various manufacturers.
To determine the molecular weights of protein antigens, to study protein/protein interactions, to determine specific enzymatic activity, to monitor protein post-translational modifications and to determine the presence and quantity of proteins.
Techniki określania masy cząsteczkowej antygenu białkowego, interakcji białkowych, aktywności enzymatycznej i modyfikacji potranslacyjnych.
Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.
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