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811D-250

Sigma-Aldrich

Human Adipocyte Differentiation Medium (250 ml)

Synonym(s):

Primary Cell Culture Media

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About This Item

UNSPSC Code:
12352207
NACRES:
NA.71

form

liquid

Quality Level

100

shelf life

6 mo.

manufacturer/tradename

Cell Applications, Inc

shipped in

wet ice

storage temp.

2-8°C

General description

Human Adipocyte Differentiation Medium

Application

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

Quality

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

Preparation Note

contained in protocol

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Rat Adipocyte Differentiation Medium (250 ml)

Sigma-Aldrich

R811D-250

Rat Adipocyte Differentiation Medium (250 ml)

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

Protocols

Human Marrow Stromal Cells (HMSC) Culture Protocol

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

Human Preadipocytes (HPAd) Culture Protocol

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

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