推薦產品
形狀
liquid
包裝
pkg of 2 x 175 μg
技術
cell culture | stem cell: suitable
儲存溫度
2-8°C
一般說明
Endothelial cells line the interior surface of blood and lymphatic vessels, forming an interface between circulating blood or lymph in the lumen and the rest of tissue or organ. Laminin-411 is known to bind to the integrin α6β1 which is located on the cell surface of pluripotent stem cells and is known to induce endothelial cell differentiation. Professor Kiyotoshi Sekiguchi′s group (Matrixome, Inc.) have produced a recombinant E8 fragment of laminin-411 at large-scale while retaining the full integrin binding activity. ECMatrix-411 E8 Laminin Substrates are recombinant Laminin-411-E8 fragments which bind to integrin α6β1 and increases the differnetiuation of pluripotent stem cells (ES/iPSCs) into acetyl-LDL+/ CD31+ endothelial cells.
應用
Xeno-free laminin-411 coating for the differentiation of pluripotent stem cells into endothelial cells, 350 μg (CHO-S derived)
包裝
350 μg (2 x 175 μg)
成分
2 X 175 μg ECMatrix-411 E8 Laminin Substrate (0.5 mg/mL in PBS). Expressed in CHO-S cells.
品質
- Purity (SDS-Page): > 95%
- Endotoxin Test: = 750 EU/mg
- Mycoplasma Test: Negative
- Sterility Test: Negative
- Integrin Binding Assay (kDa): = 10 nM
準備報告
Precoating Method
1. Dilute the 0.5 mg/mL stock solution with sterile PBS to achieve a 2.5 μg/mL working solution.
2. Coat dishes with ECMatrix-411 at 0.25 μg/cm2 (for example, for one well of a 6-well plate add 1 mL of the 2.5 μg/mL working solution).
3. Incubate for 1 hour at 37°C, 3 hours at room temperate or overnight at 4°C.
4. Before use, remove remaining fluid from the coated surface (do not rinse).
5. Detach cells into small clumps using Accutase.
6. Plate the cells at desired density.
Note: Do not allow the plates to dry, briefly spin down all liquids in the tube before use, avoid repeated freeze-thaw cycles.
1. Dilute the 0.5 mg/mL stock solution with sterile PBS to achieve a 2.5 μg/mL working solution.
2. Coat dishes with ECMatrix-411 at 0.25 μg/cm2 (for example, for one well of a 6-well plate add 1 mL of the 2.5 μg/mL working solution).
3. Incubate for 1 hour at 37°C, 3 hours at room temperate or overnight at 4°C.
4. Before use, remove remaining fluid from the coated surface (do not rinse).
5. Detach cells into small clumps using Accutase.
6. Plate the cells at desired density.
Note: Do not allow the plates to dry, briefly spin down all liquids in the tube before use, avoid repeated freeze-thaw cycles.
儲存和穩定性
ECMatrix-411 E8 Laminin Substrates should be stored at 2-8°C. Avoid multiple freeze-thaw cycles and protect from light.
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
儲存類別代碼
12 - Non Combustible Liquids
分析證明 (COA)
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