詳細說明

Lolina A/S

Address: Sindalsvej 30 8240 Risskov Danmark 

                    Email: Info@lolina.dk

Product Specification

Product Description

Lolina? Human UC-MSC Cool-Exo? Enhancer kit 1 (500×)  is a sterile, concentrated (500X) solution which contains growth factors, hormones, or proteins for directed induction of paracrine secretion. The supplement is formulated to provide an optimally balanced environment that selectively enhance the production of exosomes with anti-inflammatory properties and anti-inflammatory related miRNAs.

Preconditioning UC-MSCs with this kit aims to activate the cells' immune response pathways, leading to the secretion of exosomes with enhanced anti-inflammatory and regenerative properties. These preconditioned exosomes can be more effective in clinical applications, such as in the treatment of inflammatory diseases and tissue repair.

 Components

Instructions for Use

1. Stock solution Preparation.

Thaw all the two compounds at 37^oC. Gently tilt the tube several times to ensure complete mixing. (Note: the growth supplement may has lipoprotein precipitates; this does not affect the efficacy of the supplement). 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.  Divid the NaC2012030 into the required volumes, do not mix them. The stock solution should be stored at -20 ℃. When stored at -20℃, the stock solution is stable for 6 month.

2. Protocol

Step 1: UC-MSC Culture

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

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

Step 2: Lolina? Human UC-MSC Cool-Exo? Enhancer kit 1 Treatment

Prepare Treatment Medium:

Add the stock solution of Lolina? Human UC-MSC Cool-Exo? Enhancer kit 1 to the culture medium to a final concentration. The dilution ratio is 1:500.

Treat UC-MSCs:

Replace the regular culture medium with the treatment medium.

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

Step 3: Post-Treatment Handling

Remove Treatment Medium: After 24 hours of treatment, remove the medium containing LPS and IL-1β.

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

Conditioning Phase:

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

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

Step 4: Exosome Isolation and Purification

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

 Note

If handled improperly, some components of the medium may present a health hazard. Take appropriate precautions when handling it, including the wearing of protective clothing and eyewear. Dispose of properly.

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