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Merck
CN

917338

Sigma-Aldrich

PhotoHA-RUT

methacrylated hyaluronic acid bioink kit, with ruthenium

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别名:
3D Bioprinting, Bioink, HAMA, Hyaluronic acid
UNSPSC代码:
12352201
NACRES:
NA.23

描述

Methacrylated hyaluronic acid:
Degree of methacrylation: ≥ 45-65%

Product components :
Methacrylated hyaluronic acid (100 mg)
Ruthenium (100 mg)
Sodium persulfate photoinitiator (500 mg)

质量水平

无菌性

sterile; sterile-filtered

分子量

Mw 100-150 kDa

储存温度

−20°C

应用

PhotoHA-RUT bioink kit consists of methacrylated hyaluronic acid (HAMA) and ruthenium photoinitiator. Hyaluronic acid is the most abundant glycosaminoglycan in the body being an important component of several tissues throughout the body. While it is abundant in extracellular matrices, hyaluronic acid also contributes to tissue hydrodynamics, movement and proliferation of cells, and participates in a number of cell surface receptor interactions. The photoinitiator consists of ruthenium and sodium persulfate to be formulated in 1X cell culture media or PBS, which allows visible light photocrosslinking of the printed structure at 400-450 nm. PhotoHA-RUT provides native-like 3D HA gels, and the final gel stiffness can be customized by changing HA concentrations and crosslinking.

法律信息

PhotoHA is a trademark of Advanced BioMatrix, Inc.

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Ox. Sol. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

法规信息

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Michelle T Poldervaart et al.
PloS one, 12(6), e0177628-e0177628 (2017-06-07)
In bone regenerative medicine there is a need for suitable bone substitutes. Hydrogels have excellent biocompatible and biodegradable characteristics, but their visco-elastic properties limit their applicability, especially with respect to 3D bioprinting. In this study, we modified the naturally occurring
Sudhir Khetan et al.
Cryobiology, 90, 83-88 (2019-08-06)
While significant progress has been made in directing the behavior of cells encapsulated within three-dimensional (3D) covalently crosslinked hydrogels, the capacity of these materials to support in situ cryopreservation of cells directly within the gels has not been assessed. Here

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