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811D-250

Sigma-Aldrich

Human Adipocyte Differentiation Medium (250 ml)

Synonym(e):

Primary Cell Culture Media

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About This Item

UNSPSC-Code:
12352207
NACRES:
NA.71

Form

liquid

Qualitätsniveau

Haltbarkeit

6 mo.

Hersteller/Markenname

Cell Applications, Inc

Versandbedingung

wet ice

Lagertemp.

2-8°C

Allgemeine Beschreibung

Human Adipocyte Differentiation Medium

Anwendung

Human Adipocyte Differentiation Medium (250 ml) has been used to induce adipogenic differentiation in human pre-adipocytes.(14}

Qualität

Each lot was tested for the ability to support plating, spreading and proliferation

Angaben zur Herstellung

contained in protocol

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Masaki J Honda et al.
Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics, 111(6), 700-708 (2010-12-15)
Stem cells isolated from human dental follicles as a potential cell source for bone-tissue engineering were examined for correcting a critical bone defect. Impacted third molars were collected and single cell-derived cell populations were cultivated in growth medium. Single cell-derived
Yunxiao Liu et al.
Lab on a chip, 19(2), 241-253 (2018-12-20)
Infiltration of immune cells into adipose tissue is associated with chronic low-grade inflammation in obese individuals. To better understand the crosstalk between immune cells and adipocytes, in vivo-like in vitro models are required. Conventionally transwell culture plates are used for
Miriane de Oliveira et al.
Molecular and cellular endocrinology, 506, 110744-110744 (2020-02-07)
Triiodothyronine (T3) and irisin (I) can modulate metabolic status, increase heat production, and promote differentiation of white adipose tissue (WAT) into brown adipose tissue (BAT). Herein, human subcutaneous white adipocytes were treated with 10 nM T3 or 20 nM I for 24 h

Protokolle

Technical information for working with human marrow stromal cells including thawing, subculturing and cryopreservation

Store the cryovials in a liquid nitrogen storage tank immediately upon arrival.

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