{"product_id":"renal-cell-carcinoma-organoid-culture-abs9836","title":"Human Renal Carcinoma Organoid Culture Medium","description":"\u003ch4\u003eProduct Specification\u003c\/h4\u003e\u003cdiv class=\"responsive-table product-detail-table details-table\"\u003e\u003ctable\u003e\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eUsage\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003e\n\u003cstrong\u003e1 , original \u003c\/strong\u003e\u003cbr\u003e （ 1 Organizational recommendations after data collection are as follows: 2-8°C Stored under conditions, quickly transported to a clean laboratory for tissue processing and cell separation, photographed and information recorded. \u003cbr\u003e （ 2 Prepare several petri dishes and add...  4℃ Precooled primary culture buffer #\u003ca href=\"https:\/\/www.absin.cn\/organoid-basal-solution-\/abs9731.html\"\u003eabs9731\u003c\/a\u003e Backup. \u003cbr\u003e （ 3 Sterilize the sample bottle, place the tissue in a petri dish, wash it three times with primary culture buffer, and then cut the tissue into a volume of approximately [size missing] using ophthalmic scissors or a scalpel.  1-3mm\u003csup\u003e3\u003c\/sup\u003e  Tissue blocks. \u003cbr\u003e （ 4 The tissue is digested with digestive fluid from primary human renal cancer tissue. 37℃ oscillation digestion 15-25min (Observe the digestion situation at any time during the digestion process). \u003cbr\u003e （ 5 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, digestion was stopped by adding three times the volume of primary culture buffer. \u003cbr\u003e （ 6 ) 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 the supernatant is removed, the primary culture buffer is added for resuspension, 300g enrichment centrifugation 5min Move back to Shangqing. \u003cbr\u003e （ 7 The cell pellet contained red blood cells. Discard the supernatant and add... 1-2mL erythrocyte lysate 1-2min Then, dilute to 10mL ， 300g centrifuge 5min 。 \u003cbr\u003e （ 8 Matrix rubber calculation: No. 6 After the step, observe the collected tissue volume and add 25 double tissue volume matrix glue #abs9495 Re-hang the slab. \u003cbr\u003e （ 9 ） 24 Taking well cell culture plates as an example, each well is dispensed with gel. 25uL-30uL Tissue matrix glue mixture for board laying ( \u003cstrong\u003e Note: \u003c\/strong\u003e Matrix adhesive maintained 0-4℃ (Next operation). \u003cbr\u003e （ 10 Place the prepared culture plate in... 37℃ Incubator 10-15min After the matrix gum sets, add... 500-750uL Human renal cancer organoid medium (restored to room temperature) was cultured. \u003cbr\u003e\u003cstrong\u003e2 Organoid subculture \u003c\/strong\u003e\u003cbr\u003e （ 1 Remove the culture medium with a pipette and add to each well. 1-2mL 4℃ organoid subculture buffer #\u003ca href=\"https:\/\/www.absin.cn\/organoid-basal-solution-\/abs9730.html\"\u003eabs9730\u003c\/a\u003e placement 2min 。 \u003cbr\u003e （ 2 Gently blow the matrix glue with a pipette to collect... 15mL In the centrifuge tube, 4℃ standing 10-15min 。 (each 6-8 (The holes are a group) \u003cbr\u003e （ 3 ） a : Insufficient number or small volume of organoids: 300g centrifuge 5min Discard the supernatant and add 1mL organoid subculture buffer resuspension and transfer 1.5mL centrifuge tube, 300g centrifuge 5min Discard the liquid for the first 4 step. \u003cbr\u003e         b When the number of organoids is large or the volume is large: 300g centrifuge 5min Discard the supernatant and add 1-2mL organoid passage digestive fluid #\u003ca href=\"https:\/\/www.absin.cn\/organoid-digestion-solution\/abs9520.html\"\u003eabs9520\u003c\/a\u003e digestion 2-4min , add 3 Organoid subculture buffer twice the volume of organoid digestive fluid terminates digestion, 300g centrifuge 5min Discard the supernatant, add an appropriate amount of organoid subculture buffer, resuspend and transfer. 1.5mL centrifuge tube, 300g centrifuge 5min Abandon the Shangqing and proceed with the first 4 step. \u003cbr\u003e （ 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 。 After the matrix gum sets, add to each well 500-750uL Organoid medium for human renal cancer. \u003cbr\u003e\u003cstrong\u003e3 Organoid cryopreservation \u003c\/strong\u003e\u003cbr\u003e （ 1 Remove the culture medium with a pipette and add to each well. 1-2mL 4℃ organoid subculture buffer placement 2min 。 \u003cbr\u003e （ 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) \u003cbr\u003e （ 3 Centrifugation 5min Discarding the supernatant, adding an appropriate amount of organoid subculture buffer to resuspend again, 300g centrifuge 5min Discard the liquid. \u003cbr\u003e （ 4 ) each 3 Hole addition 2mL organoid cryopreservation fluid #\u003ca href=\"https:\/\/www.absin.cn\/organoid-cryopreservation-medium\/abs9519.html\"\u003eabs9519\u003c\/a\u003e Gently blow and mix well, then transfer to cell cryopreservation tubes. Each tube... 1mL 。 \u003cbr\u003e （ 5 After marking the information, performing program cooling, move to... -80°C In the refrigerator, 48h Then, it was transferred to liquid nitrogen for long-term storage. Or put in 4℃ refrigerator 40min Then, put in -20℃ in the refrigerator 2h , move to -80℃ In the refrigerator, 48h Afterwards, it was placed in a liquid nitrogen tank for storage. \u003cbr\u003e\u003cstrong\u003e4 Organoid resuscitation \u003c\/strong\u003e\u003cbr\u003e （ 1 ) take 10mL organoid subculture buffer 15mL In the centrifuge tube. \u003cbr\u003e （ 2 Remove the frozen organoid cells from the liquid nitrogen tank and quickly place them in...  37℃ Melt in a water bath. \u003cbr\u003e （ 3 During the water bath thawing process, the freezing tube should be gently shaken to ensure that the cryopreservation solution is completely thawed in a short time. \u003cbr\u003e （ 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 to resuspend, and transfer in 1.5mL centrifuge tube 300g centrifuge 5min Abandon the Shangqing Dynasty. \u003cbr\u003e （ 5 ) Add per cryopreservation tube 100ul Matrix gel resuspension, per well 25uL Matrix glue is laid on 24 In well cell culture plates, place in an incubator. 10-15min Gelation, addition 500-750uL Organoid medium for human renal cancer. \u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eStorage Temp.\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eStore at -20°C with a shelf life of 1 year.\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\u003c\/table\u003e\u003c\/div\u003e","brand":"Absin","offers":[{"title":"100mL","offer_id":43224148213835,"sku":"abs9836-100mL","price":476.0,"currency_code":"USD","in_stock":true},{"title":"500mL","offer_id":43224148246603,"sku":"abs9836-500mL","price":1587.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.antbioinc.com\/products\/renal-cell-carcinoma-organoid-culture-abs9836","provider":"AntBio","version":"1.0","type":"link"}