HEPES (1 M)
HEPES (1 M)
HEPES (1 M)
HEPES (1 M)
Gibco™

HEPES (1 M)

Gibco™ HEPES N-2-Hydroxyethylpiperazin-N-2-ethansulfonsäure) ist ein zwitterionisches, organisches, chemisches Puffermittel, das häufig in Zellkulturmedien eingesetzt wird. Die Zugabe von 10 bisWeitere Informationen
Have Questions?
Ansicht ändernbuttonViewtableView
KatalognummerMenge
15630080100 mL
1563010620 mL
Katalognummer 15630080
Preis (EUR)
138,00
Each
Zum Warenkorb hinzufügen
Menge:
100 mL
Preis (EUR)
138,00
Each
Zum Warenkorb hinzufügen
Gibco™ HEPES N-2-Hydroxyethylpiperazin-N-2-ethansulfonsäure) ist ein zwitterionisches, organisches, chemisches Puffermittel, das häufig in Zellkulturmedien eingesetzt wird. Die Zugabe von 10 bis 25 mM HEPES-Puffer sorgt für zusätzliche Pufferkapazität, wenn sich die Zellkultur für längere Manipulationsperioden außerhalb des CO2-Inkubators befindet. HEPES-Puffer ist eine gute Wahl für viele Zellkultursysteme, da es membranundurchlässig ist, weniger Auswirkungen auf biochemische Reaktionen hat, chemisch und enzymatisch stabil ist und sich durch geringe Licht- und UV-Absorption auszeichnet.

cGMP-Fertigung an zwei Standorten
Gibco™ HEPES wird in einer cGMP-konformen Einrichtung hergestellt, die sich sich in Paisley, Schottland (Großbritannien) befindet. Die Einrichtung ist von der US-Arzneimittelbehörde FDA als Hersteller von Medizinprodukten zugelassen und nach ISO 13485-zertifiziert. Um lückenlose Versorgung zu sichern, bieten wir ein identisches Gibco™ HEPES-Produkt an, das an unserem Standort in Grand Island (USA) hergestellt wird (15630-080). Diese Einrichtung ist von der US-Arzneimittelbehörde FDA als Hersteller von Medizinprodukten zugelassen und nach ISO 13485-zertifiziert.
Für die Verwendung in der Forschung oder die Weiterverarbeitung. Nicht zur Diagnosestellung oder direkten Anwendung bei Menschen oder Tieren geeignet.
Specifications
Chemischer Name oder MaterialZwitterionischer organischer chemischer Puffer
FarbeKlar
ZusammensetzungN-2-Hydroxyethylpiperazin-N-2-Ethan-Sulfonsäure
Empfohlene LagerungLagerbedingungen: 2 bis 8 °C
Versandbedingungen: Haltbarkeit bei
Raumtemperatur: 24 Monate ab Herstellungsdatum
SterilitätSteril gefiltert
SterilisationsmethodeSterile-filtered
Zur Verwendung mit (Anwendung)Chromatin-Biologie, Säugetierzellkultur
GüteBiochemie
Physikalische FormFlüssigkeit
Menge100 mL
LösungstypPufferlösung
Unit SizeEach

Häufig gestellte Fragen (FAQ)

Based on the Sodium bicarbonate levels in the medium, what CO2 % is recommended?

If the media formulation contains:

NaHCO3 (g/L) < 1.5, it needs CO2 at 4%;
NaHCO3 (g/L) 1.5 – 2.2, it needs CO2 at 5%;
NaHCO3 (g/L) 2.2 - 3.4, it needs CO2 at 7%;
NaHCO3 (g/L) > 3.5, it needs CO2 at 10% .

*There are some exceptions. Gibco DMEM has always been made according to Dulbecco’s original published formulation, with 3.7 g/L sodium bicarbonate. Customers have been using this medium in CO2 incubators ranging from 5-10% CO2 for decades, usually with no trouble maintaining physiological pH. This also depends on the cell type. Once cells are growing, the pH will drop (due to metabolic accumulation of lactic acid).

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

Do high or low levels of sodium bicarbonate affect the pH of my tissue culture media?

Sodium bicarbonate is necessary to control the pH of the solution. To maintain physiological pH, the concentration of the sodium bicarbonate in the medium must be matched with the right level of CO2 in the atmosphere above the medium in the incubator*.

If the sodium bicarbonate is high and the CO2 concentration is low, the pH will become alkaline. This is something that you will see in a bottle of media when it is exposed to air for long periods or when there is a lot of head space in the bottle. The media color will be pinkish or purplish. When this media is put back into a CO2 incubator, the color/pH will change back to the normal orangeish/reddish color or physiological pH.

If the sodium bicarbonate is low and the CO2 is high, the pH will become acidic. This is something you will see when you put medium into a 5% or 10% CO2 incubator.

*There are some exceptions. For instance, Gibco DMEM has always been made according to Dulbecco’s original published formulation, with 3.7g/L sodium bicarbonate. Customers have been using this medium in CO2 incubators ranging from 5-10% CO2 for decades, usually with no trouble maintaining physiological pH. this also depends on the cell type, Once cells are growing, the pH will drop (due to metabolic accumulation of lactic acid).

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

My Gibco HEPES (1M) (Cat. No. 15630080) was accidentally frozen. Can I still use it?

This product should be stored at 2-8 degrees C and should not be frozen. The biggest issue with accidentally freezing this product is its solubility. If this product was accidentally frozen, we recommend placing it in a 2-8 degree environment and allowing it to slowly thaw overnight. If the product is fully thawed and shows no signs of precipitation, then it should still be usable, but we cannot guarantee effectiveness.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

Is HEPES (1 M) in distilled water or in saline solution?

1M HEPES is in water with a pH range of 7.2 - 7.5.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

What is the endotoxin specification for HEPES (1 M) (Cat. Nos. 15630080, 15630106, and 15630130)?

Sorry, we do not test endotoxin levels for this product.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

Zitierungen und Referenzen (6)

Zitierungen und Referenzen
Abstract
A comparison between different human hepatocyte models reveals profound differences in net glucose production, lipid composition and metabolism in vitro.
Authors:Bonanini F,Singh M,Yang H,Kurek D,Harms AC,Mardinoglu A,Hankemeier T
Journal:Experimental cell research
PubMed ID:38499143
Preparation and characterization of toxic Abeta aggregates for structural and functional studies in Alzheimer's disease research.
Authors:Jan A, Hartley DM, Lashuel HA,
Journal:Nat Protoc
PubMed ID:20539293
'The amyloid cascade hypothesis, supported by strong evidence from genetics, pathology and studies using animal models, implicates amyloid-beta (Abeta) oligomerization and fibrillogenesis as central causative events in the pathogenesis of Alzheimer''s disease (AD). Today, significant efforts in academia, biotechnology and the pharmaceutical industry are devoted to identifying the mechanisms by ... More
Investigating conversion of mechanical force into biochemical signaling in three-dimensional chondrocyte cultures.
Authors:Bougault C, Paumier A, Aubert-Foucher E, Mallein-Gerin F,
Journal:Nat Protoc
PubMed ID:19478808
The culture of chondrocytes embedded within agarose hydrogels maintains chondrocytic phenotype over extended periods and allows analysis of the chondrocyte response to mechanical forces. The mechanisms involved in the transduction of a mechanical stimulus to a physiological process are not completely deciphered. We present protocols to prepare and characterize constructs ... More
Molecular rearrangements of the extracellular vestibule in NMDAR channels during gating.
Authors: Sobolevsky Alexander I; Beck Christine; Wollmuth Lonnie P;
Journal:Neuron
PubMed ID:11779481
Many N-methyl-D-aspartate receptor (NMDAR) channel blockers that have therapeutic potential can be trapped in the closed state. Using a combination of the substituted cysteine accessibility method and open channel blockers, we found that the M3 segment forms the core of the extracellular vestibule, including a deep site for trapping blockers. ... More
Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells.
Authors:Scheffers MS, van der Bent P, Prins F, Spruit L, Breuning MH, Litvinov SV, de Heer E, Peters DJ,
Journal:Hum Mol Genet
PubMed ID:11063733
Polycystin-1 is a novel protein predicted to be a large membrane-spanning glycoprotein with an extracellular N-terminus and an intracellular C-terminus, harboring several structural motifs. To study the subcellular localization, antibodies raised against various domains of polycystin-1 and against specific adhesion complex proteins were used for two-color immunofluorescence staining. In Madine ... More