{"id":18501,"date":"2021-07-20T11:06:51","date_gmt":"2021-07-20T02:06:51","guid":{"rendered":"http:\/\/mus.brc.riken.jp\/en\/?page_id=18501"},"modified":"2021-07-20T11:06:51","modified_gmt":"2021-07-20T02:06:51","slug":"jul_2021","status":"publish","type":"page","link":"http:\/\/mus.brc.riken.jp\/en\/current_tech\/jul_2021","title":{"rendered":"BRC Current Technology July 2021"},"content":{"rendered":"\n\n\n\n\n
\"RIKEN<\/td>\nBRC Current Technology<\/span>
\nJuly 2021<\/span><\/a><\/td>\n<\/tr>\n
\n

16. Ultraeasy mouse sperm freezing method for everyone<\/h1>\n

No LN2<\/sub>, special reagents, containers and techniques;
useful in emergency situations<\/h2>\n

Cryopreservation of mouse spermatozoa is widely used for the efficient preservation and safe transport of valuable mouse strains. However, the current cryopreservation method requires special containers (plastic straws), undefined chemicals (skim milk), liquid nitrogen, and expertise when handling sperm suspensions. Here, we introduce an easy and quick (EQ) sperm freezing method. The main procedure consists of only one step: dissecting a single cauda epididymis in a microtube containing 20% raffinose solution, which is then stored in a \u201380 \u00b0C freezer. The frozen spermatozoa retain practical fertilization rates after 1 (51%) or even 3 months (25%) with the C57BL\/6J strain, the most sensitive strain for sperm freezing. More than half of the embryos thus obtained developed into offspring after embryo transfer. Importantly, spermatozoa stored at \u201380 \u00b0C can be transferred into liquid nitrogen for indefinite storage.
\n  As far as we know, our EQ method is the easiest and quickest method for mouse sperm freezing and should be applicable in all laboratories without expertise in sperm cryopreservation. This EQ method can help avoid the loss of irreplaceable strains because of closure of animal rooms in emergency situations such as unexpected microbiological contamination or social emergencies such as the COVID-19 threat.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>\n\n\n\n\n
Reference:<\/td>\n<\/tr>\n
<\/td>\nK. Mochida et al. \u201cEasy and quick (EQ) sperm freezing method for urgent preservation of mouse strains\u201d Sci Rep.<\/i> 2021 Jul 8;11(1):14149. DOI: 10.1038\/s41598-021-93604-y.<\/a>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

BRC Current Technology July 2021 16. Ultraeasy mouse sperm freezing method for everyone No LN2, special reagents, containers and techniques; useful in emergency situations Cryopreservation of mouse spermatozoa is widely used for the efficient preservation and safe transport of valuable mouse strains. However, the current cryopreservation method requires special containers (plastic straws), undefined chemicals (skim milk), liquid nitrogen, and expertise when handling sperm suspensions. Here, we introduce an easy and quick (EQ) sperm freezing method. The main procedure consists of only one step: dissecting a single cauda epididymis in a microtube containing 20% raffinose solution, which is then stored in a \u201380 \u00b0C freezer. The frozen spermatozoa retain practical fertilization rates after 1 (51%) or even 3 months (25%) with the C57BL\/6J strain, the most sensitive strain for sperm freezing. More than half of the embryos thus obtained developed into offspring after embryo transfer. Importantly, spermatozoa stored at \u201380 \u00b0C can be transferred into liquid nitrogen for indefinite storage.   As far as we know, our EQ method is the easiest and quickest method for mouse sperm freezing and should be applicable in all laboratories without expertise in sperm cryopreservation. This EQ method can help avoid the loss of irreplaceable […]<\/p>\n","protected":false},"author":19,"featured_media":0,"parent":3268,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","_seopress_robots_follow":"","_seopress_robots_imageindex":"","_seopress_robots_snippet":"","_seopress_robots_primary_cat":"","_seopress_robots_breadcrumbs":"","_seopress_robots_freeze_modified_date":"","_seopress_robots_custom_modified_date":"","_seopress_robots_canonical":"","_seopress_social_fb_title":"","_seopress_social_fb_desc":"","_seopress_social_fb_img":"","_seopress_social_fb_img_attachment_id":0,"_seopress_social_fb_img_width":0,"_seopress_social_fb_img_height":0,"_seopress_social_twitter_title":"","_seopress_social_twitter_desc":"","_seopress_social_twitter_img":"","_seopress_social_twitter_img_attachment_id":0,"_seopress_social_twitter_img_width":0,"_seopress_social_twitter_img_height":0,"_seopress_redirections_value":"","_seopress_redirections_enabled":"","_seopress_redirections_enabled_regex":"","_seopress_redirections_logged_status":"","_seopress_redirections_param":"","_seopress_redirections_type":301,"_seopress_analysis_target_kw":"","footnotes":"","_wp_rev_ctl_limit":""},"class_list":["post-18501","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/pages\/18501","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/users\/19"}],"replies":[{"embeddable":true,"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/comments?post=18501"}],"version-history":[{"count":1,"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/pages\/18501\/revisions"}],"predecessor-version":[{"id":18502,"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/pages\/18501\/revisions\/18502"}],"up":[{"embeddable":true,"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/pages\/3268"}],"wp:attachment":[{"href":"http:\/\/mus.brc.riken.jp\/en\/wp-json\/wp\/v2\/media?parent=18501"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}