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Mouse ovary Organoid Culture Kit

Mouse ovary Organoid Culture Kit

Catalog Number: abs9754 Brand: Absin
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$1,083 USD
$1,083 USD
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Product Specification

Usage 1 , original
（ 1 Normal ovarian tissue from mice after sampling must be in 2 - 8℃ Wash, prepare several petri dishes, and add 4℃ Precooled primary culture buffer B Standby (added bispecific antibody and gentamicin).
（ 2 Tissues were placed in petri dishes using primary culture buffer. B After three cleanings, the tissue is cut into a volume of approximately... using ophthalmic scissors or a scalpel. 1-3 mm3 Tissue blocks.
（ 3 Digestive fluid of normal ovarian primary tissue in mice for tissue use C digestion, 37℃ oscillation digestion 15-20 min (Observe the digestion situation at any time during the digestion process).
（ 4 Take a small amount of liquid and observe it under a microscope. A large number of individual cells or 70um After the following cell clusters, add three times the volume of primary culture buffer B Termination of digestion.
（ 5 ) Use 100um The filtrate is filtered using a sieve with a certain pore size, and the filtrate is collected and then... 300g enrichment centrifugation 5min Then remove the supernatant and add primary culture buffer B Resuspend and centrifuge.
（ 6 Matrix rubber calculation: No. 6 After the step, observe the collected tissue volume and add 25-30 Matrix glue with twice the tissue volume ( abs9495 Resuspend the slab.
（ 7 ） 24 Taking well cell culture plates as an example, each well is dispensed with gel. 25uL Tissue matrix glue mixture for board laying ( 4℃ (Next operation).
（ 8 Place the prepared culture plate in... 37℃ Incubator 10-15min Gelatinization, addition of mouse normal ovary organoid medium A (Return to room temperature) for incubation.
2 Organoid subculture
（ 1 Remove the culture medium with a pipette and add to each well. 1-2mL 4℃ organoid subculture buffer G placement 2min 。
（ 2 Gently blow the matrix glue with a pipette to collect... 15mL In the centrifuge tube, 4℃ standing 10min 。 (each 6-8 (The holes are a group)
（ 3 ） a : Insufficient number or small volume of organoids: centrifuge 5min Discard the supernatant and add an appropriate amount of organoid subculture buffer G Resuspend and move in 1.5mL centrifuge tube, 300g centrifuge 5min Discard the liquid for the first 4 step.
         b When the number or volume of organoids is large: Centrifuge 5min Discard the supernatant and add an appropriate amount of organoid passage digestion solution. D digestion 2-3min Add organoid subculture buffer G Terminate digestion and centrifuge 5min Discard the mixture and add an appropriate amount of organoid subculture buffer G Resuspend and move in 1.5mL centrifuge tube, 300g centrifuge 5min Discard the liquid for the first 4 step.
（ 4 After organoids were collected, matrix gel was added for resuspension, and each well was resuspended. 25uL Matrix glue is laid on 24 In well cell culture plates, place in an incubator. 10-15min Add 500uL mouse normal ovarian organoid culture medium A 。
3 Organoid cryopreservation
（ 1 Remove the culture medium with a pipette and add to each well. 1-2mL 4℃ organoid subculture buffer G placement 2min 。
（ 2 Gently blow the matrix glue with a pipette to collect... 15mL In the centrifuge tube, 4℃ standing 10min 。 (each 6-8 (The holes are a group)
（ 3 Centrifugation 5min Discard the supernatant and add an appropriate amount of organoid subculture buffer G Hanging again, 300g centrifuge 5min Discard the liquid.
（ 4 Add an appropriate amount of organoid cryopreservation solution. F Gently blowing and resuspending, 24 Taking well cell culture plates as an example: the density is 2 Individual hole cryopreservation 1 Tubes, volume per tube 1.4mL 。
（ 5 Mark the information, cool it down procedurally, and then transfer it to liquid nitrogen for long-term storage.
4 Organoid resuscitation
（ 1 ) take 10ml organoid subculture buffer G At 15mL In the centrifuge tube.
（ 2 Remove the frozen organoid cells from the liquid nitrogen tank and quickly place them in... 37℃ Melt in a water bath.
（ 3 During the water bath thawing process, the freezing tube needs to be gently shaken to ensure that the cryopreservation solution is... 1-2min It completely dissolves inside.
（ 4 ) Rapidly transfer the lysed organoid cells to 15mL Centrifuge tube, gently blow with a pipette 6-8 next time, 300g centrifuge 5min The supernatant is then removed and the organoid cell pellet is collected. Add an appropriate amount of organoid subculture buffer G Resuspend and move in 1.5mL centrifuge tube 300g centrifuge 5min 。
（ 5 Resuspend the matrix gel, per well 25uL Matrix glue is laid on 24 In well cell culture plates, place in an incubator. 10-15min Gelation, addition 500uL mouse normal ovarian organoid culture medium A 。
Description Kit Composition:
Component Name Specification
mouse normal ovarian organoid culture medium A 100mL
primary culture buffer B 250mL
Digestive fluid of normal ovarian primary tissue in mice C 30mL
organoid passage digestive fluid D 30mL
tissue preservation solution E 100mL
organoid cryopreservation fluid F 20mL
organoid subculture buffer G 250mL
Storage Temp. Store at -20°C with a shelf life of 1 year.

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Immunohistochemistry