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

HEPES (1M)

HEPES (N-2-hidroxietilopiperacina-N-2-etano ácido sulfónico) Gibco™ es un agente tamponador de origen químico orgánico de zwitterión que se suele emplear enMás información
Have Questions?
Cambiar vistabuttonViewtableView
Número de catálogoCantidad
15630080100 mL
1563010620 mL
1563013020 x 100 mL
Número de catálogo 15630080
Precio (MXN)
2,122.60
Each
Añadir al carro de la compra
Cantidad:
100 mL
Precio (MXN)
2,122.60
Each
Añadir al carro de la compra
HEPES (N-2-hidroxietilopiperacina-N-2-etano ácido sulfónico) Gibco™ es un agente tamponador de origen químico orgánico de zwitterión que se suele emplear en medios de cultivo celular. La adición de 10–25 mM de HEPES proporciona una mayor capacidad de tampón cuando el cultivo celular requiere largos periodos de manipulación fuera de una incubadora de CO2. HEPES es una buena elección de tamponamiento para muchos sistemas de cultivo celular, ya que su membrana impermeable tiene un efecto limitado sobre las reacciones bioquímicas, es químicamente y enzimáticamente estable y tiene muy baja absorbancia de luz ultravioleta y visible.

Sistema de calidad y fabricación conforme a las prácticas recomendadas de fabricación actuales en dos instalaciones
HEPES Gibco™ se fabrica en instalaciones que cumplen con las prácticas recomendadas de fabricación actuales, ubicadas en Paisley, Escocia (Reino Unido) Las instalaciones están registradas en la Agencia estadounidense de alimentos y medicamentos (FDA) como fabricante de dispositivos médicos y están certificadas según la norma ISO 13485. Para la continuidad de la cadena de suministro, ofrecemos un producto de HEPES Gibco™ idéntico fabricado en nuestras instalaciones de Grand Island (EE. UU.) (15630-080). Estas instalaciones se han registrado en la FDA como fabricante de dispositivos médicos y tienen la certificación según la norma ISO 13485.
Para su uso en investigación o procesos de fabricación posteriores. No apto para uso diagnóstico ni para la administración directa en seres humanos ni en animales.
Especificaciones
Nombre del producto químico o materialTampón químico orgánico zwitteriónico
ColorTransparente
FormulaciónN-2-hidroxietilopiperacina-N-2-etano ácido sulfónico
Almacenamiento recomendadoCondiciones de almacenamiento: De 2 °C a 8 °C
Condiciones de envío: Temperatura ambiente
Vida útil: 24 meses a partir de la fecha de fabricación
EsterilidadSterile
Método de esterilizaciónSterile-filtered
Para utilizar con (aplicación)Biología de la cromatina, cultivo celular de mamíferos
GradoBioquímica
Forma físicaLíquido
Cantidad100 mL
Tipo de soluciónSolución de tampón
Unit SizeEach

Preguntas frecuentes

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.

Citations & References (6)

Citations & References
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