詳細說明

Lolina A/S

Address: Sindalsvej 30 8240 Risskov Danmark 

                    Email: Info@lolina.dk

Product Specification

Product Description

Lolina? Human BM-MSC heal-Exo? enhancer kit 2  is a set of sterile powders or concentrated solution which contains growth factors, hormones, or proteins for directed induction of paracrine secretion and exosome protection.

As an treatments additive for BM-MSC in vitro culture, this supplement has been proved has following functions:

1.         Strongly active the paracrine secretion of anti-inflammatory exosomes.

2.         Exos produced under this condition showed excellent ability to promote wound regeneration by promoting angiogenesis without affecting liver and kidney function.

3.         At the same time, ATV-Exos promoted the proliferation, migration, tube formation and VEGF levels of endothelial cells in vitro.Enhance the stability of MSCs.

4.         The robustness of exosomes can be increased by enhancing the robustness of the exosome membrane.

5.         Enhance the stress response pathway within MSCs to improve the robustness of exosomes.

Components

Instructions for Use

1. Stock solution Preparation.

One kit is for 50ml cell culture medium.

a.         NaC20130305-A is a ready-to-use reagent, just and it into treatment medium to obtain desire concentration.

b.         NaC20130305-B/C are offered as powder, their stock solutions are prepared as follows:

The compounds are offered as powder in tubes. Please centrifuge before opening the cap to ensure the accuracy of the dosage.

Please carry out dissolution and packaging operations on a clean bench.

Spray the medium bottle and supplement tube with 70% ethanol and wipe to remove excess liquid. In a sterile field, remove the caps without touching the interior  threads  with  fingers. 

Reconstitute NaC20130305-B in 10 μl sterile DMSO/enthonal. Aliquot into appropriate volumes of storage solution. Aliquot into appropriate volumes of storage solution. When stored at -20℃, the stock solution is stable for 4 years. When stored at 4 ℃, the stock solution is stable for 1 week.

Reconstitute NaC20130305-C in sterile 0.9% NaCl solution/base culture medium. The recommend volume is 5 mL. Aliquot into appropriate volumes of storage solution. When stored at 2-8 ℃, -20℃, the stock solution is stable for 24 month.  

2. Protocol

Step 1: BM-MSC Culture

Seeding: Seed BM-MSC in culture flasks or plates at a density allowing them to reach 70-80% confluence.

Growth: Allow BM-MSC to grow until they reach the desired confluence.

Step 2: Pre-treatment with NaC20130305-A

Prepare pre-Treatment Medium:

a.         Add the stock solution of NaC20130305-A to the culture medium to a final concentration. The dilution ratio range is from 0.3:50 to 1.13:50.

[Notes]: Please determine the optimal treatment concentration by setting up preliminary experiments to avoid cell damage caused by excessively high concentrations, which may lead to cell detachment and death.

Pre-treat BM-MSCs:

b.         Replace the medium by the pre-treatidng medium. Treating cells for 2h under standard culture conditions (37 ℃, 5% CO₂).

Step 3: Treatment BM-MSC with NaC20130305-B/C

Prepare Treatment Medium:

c.         Thaw the stock solution.

d.        Add the stock solution of NaC20130305-B/C to the regular culture medium to obtain a treatment medium. The dilution ratio is: NaC20130305-B  1:5000; NaC20130305-C  1:10.

Treat BM-MSCs:

e.         Replace the regular culture medium with the treatment medium.

f.         Incubate the BM-MSCs with the treatment medium for 24 hours under standard culture conditions (37 ℃, 5% CO2).

Step 3: Post-Treatment Handling

g.         Remove Treatment Medium: After 24 hours of treatment, remove the treatment medium.

h.        Wash MSCs: Wash the cells gently with PBS to remove any residual the treatment medium.

Conditioning Phase:

i.          Replace with fresh, serum-free, or exosome-depleted medium.

j.          Incubate the BM-MSCs for an additional 24-48 hours to collect the conditioned medium containing exosomes.

Step 4: Exosome Isolation and Purification

k.        Collect the conditioned medium after the post-treatment incubation period.

Note