推荐产品
品質等級
化驗
>98% (TLC)
形狀
powder
顏色
white to off-white
溶解度
0.5 M HCl: 50 mg/mL, clear, colorless to faintly yellow
正離子痕跡
Ca: 15.0-22.8% (Dry basis)
SMILES 字串
OCC(OP(O)(O)=O)CO.[Ca]
InChI
1S/C3H9O6P.Ca.2H/c4-1-3(2-5)9-10(6,7)8;;;/h3-5H,1-2H2,(H2,6,7,8);;;
InChI 密鑰
DVIIMTRPWRJOMF-UHFFFAOYSA-N
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Ashraf Saif et al.
Drug discoveries & therapeutics, 6(6), 315-320 (2013-01-23)
Human osteosarcoma cell line SaOS-2 is an osteoblastic cell model that contains factors like bone morphogenetic proteins necessary for initiating bone formation. The cell line also expresses high levels of osteoinductive activity. In contrast to highly complicated and expensive ways
Mingyue Liu et al.
Molecules (Basel, Switzerland), 17(2), 1219-1232 (2012-02-02)
Dentinogenesis is a necessary prerequisite for dental tissue engineering. One of the steps for dentinogenesis is to obtain large quantities of highly purified odontoblasts. Therefore, we have undertaken an experiment applying different concentrations of β-glycerophosphate (β-GP) to induce the differentiation
Hong-Xing Shi et al.
Huan jing ke xue= Huanjing kexue, 32(10), 2916-2919 (2012-01-28)
Effect of phosphorus on the production of microcystin was researched. The effects of soluble reactive phosphorus (SRP) on the growth of cells and on the production of Microcystin were studied. In addition, the efficiency of four different phosphorus compounds was
Effects of osteogenic differentiation inducers on in vitro expanded adult mesenchymal stromal cells.
Elisa Fiorentini et al.
The International journal of artificial organs, 34(10), 998-1011 (2011-12-14)
For bone regeneration therapy using stem cells, well-defined ex vivo protocols to expand mesenchymal stromal cells (MSC), as well as assays to show their potential differentiation into the osteogenic lineage, are needed. Aim of this study was to analyze the
N Z Sun et al.
The Journal of international medical research, 40(2), 761-767 (2012-05-23)
To investigate the capability of human placenta-derived adherent cells to differentiate into osteocytes and adipocytes. Placenta-derived adherent cells were isolated by type IV collagenase digestion of a single freshly obtained human placenta and cultured under standard conditions. Cell surface markers
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