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Merck

S4920

Sigma-Aldrich

SITE Liquid Media Supplement (100×)

liquid, sterile-filtered, BioReagent, suitable for cell culture

Sinónimos:

Media supplement

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5 ML
MXP 1,079.00

MXP 1,079.00


Fecha estimada de envío01 de junio de 2025


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5 ML
MXP 1,079.00

About This Item

Código UNSPSC:
12352205
NACRES:
NA.75

MXP 1,079.00


Fecha estimada de envío01 de junio de 2025


Solicitar un pedido a granel

esterilidad

sterile-filtered

Línea del producto

BioReagent

Formulario

liquid

técnicas

cell culture | mammalian: suitable

impurezas

endotoxin, tested

Condiciones de envío

ambient

temp. de almacenamiento

2-8°C

Descripción general

SITE Liquid Media Supplement (100×) serves as a substitute for serum-free formulations. It contains purified factors required for in vitro growth and differentiation studies. The addition of supplements to media will vary, depending on the cell type being studied and the basal medium employed. It is a general cell supplement designed for use in non-complex media (e.g., minimum essential medium (MEM), Roswell Park Memorial Institute Medium (RPMI-1640)) and complex media (e.g., Ham′s F-12, Dulbecco′s Modified Eagle Medium (DME) /F-12, MEM) with sodium pyruvate.

Aplicación

SITE Liquid Media Supplement (100×) has been used:
  • in the 3D culture of mouse embryonic pancreatic epithelial cells[1]
  • to isolate rabbit gastric glands and parietal cells[2]
  • to isolate rabbit single proximal tubule cells[3]

Acciones bioquímicas o fisiológicas

  • Insulin: a polypeptide hormone that promotes the uptake of glucose and amino acids and may owe an observed mitogenic effect to this property.[4]
  • Transferrin: an iron-transport protein. Iron is an essential trace element but can be toxic in its free form. To nourish cells in culture, iron is supplied bound to transferrin in serum.[5]
  • Selenium: an essential trace element normally provided by serum.[6]
  • Ethanolamine: plays a significant role in the proliferation of hybridoma cells and frequently is added to supplements used for culturing these cells.[7]

Componentes

Contains 1.0mg/ml recombinant human insulin, 0.55mg/ml human transferrin (substantially iron-free), 0.5μg/ml sodium selenite and 0.2mg/ml ethanolamine at the 100x concentration.

Nota de preparación

Prepared in Earle′s Balanced Salt Solution (EBSS) without phenol red.

Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Lixin Zhu et al.
American journal of physiology. Cell physiology, 295(1), C192-C202 (2008-05-16)
In a comparison of three different tissues, the membrane cytoskeleton linker protein ezrin was found to assume high levels of phosphorylation on threonine-567 (T567) in the brush border membranes of renal proximal tubule cells and small intestine enterocytes, in contrast
H Murakami et al.
Proceedings of the National Academy of Sciences of the United States of America, 79(4), 1158-1162 (1982-02-01)
A serum-free medium supplemented with a few growth factors was devised to grow lymphocyte hybridomas. The medium was developed with the hybridoma line MPC11-BL, a fusion product between a mouse plasmacytoma cell line (MPC11TG70na3) and mouse (BALB/c) spleen cells. In
Lixin Zhu et al.
American journal of physiology. Cell physiology, 293(3), C874-C884 (2007-06-08)
In its dormant state, the membrane cytoskeletal linker protein ezrin takes on a NH(2) terminal-to-COOH terminal (N-C) binding conformation. In vitro evidence suggests that eliminating the N-C binding conformation by Thr(567) phosphorylation leads to ezrin activation. Here, we found for
Nico Laur et al.
PloS one, 15(5), e0233357-e0233357 (2020-05-21)
Trace elements and minerals are compounds that are essential for the support of a variety of biological functions and play an important role in the formation of and the defense against oxidative stress. Here we describe a technique, allowing sequential
Mostafa Bakhti et al.
Molecular metabolism, 30, 16-29 (2019-11-27)
Translation of basic research from bench-to-bedside relies on a better understanding of similarities and differences between mouse and human cell biology, tissue formation, and organogenesis. Thus, establishing ex vivo modeling systems of mouse and human pancreas development will help not only

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