<u id="oqj1j"><font id="oqj1j"></font></u>

<pre id="oqj1j"></pre>

      1. <table id="oqj1j"></table>
          女人18毛片a级毛片免费视频,亚洲成人av免费一区,国产亚洲综合久色av,在线看片免费人成视频播,久草国产在线观看,久久高清超碰AV热热久久,亚洲色偷偷色噜噜狠狠99,无遮挡国产高潮视频免费观看
          您好!歡迎訪問上海起發實驗試劑有限公司網站!
          全國服務咨詢熱線:

          15921799099

          當前位置:首頁 > 產品中心 > 代理品牌 > 國際品牌 > Proteus BioSciences 25-6790 - Myosin-VIIa 現貨供應

          Proteus BioSciences 25-6790 - Myosin-VIIa 現貨供應

          簡要描述:Proteus BioSciences was founded in 2002 to develop innovative products to advance proteomic research. We specialize in discovering peptides and proteins with novel biological properties

          • 產品型號:
          • 廠商性質:代理商
          • 更新時間:2025-12-31
          • 訪  問  量:6077

          詳細介紹

          Myosin-VIIa

          Rabbit Polyclonal Antibody

          PRODUCT #: 25-6790

           

          DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 
           

          SPECIES CROSS-REACTIVITY:

          Human, mouse, rat, pig, avian, amphibian
           

          APPLICATIONS/DILUTIONS:

          IF (5-10 ug/ml)
          WB (0.5-1.0 ug/ml)
           

          SOURCE:

          Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.
           

          FORM/STORAGE:

          50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20º C.  Avoid multiple freeze/thaw cycles.
           

          References:
          Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
          Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
          Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
          Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.
           

          DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 
           
          SPECIES CROSS-REACTIVITY:
          Human, mouse, rat, pig, avian, amphibian
           
          APPLICATIONS/DILUTIONS:
          IF (5-10 ug/ml)
          WB (0.5-1.0 ug/ml)
           
          SOURCE:
          Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.
           
          FORM/STORAGE:
          50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20º C.  Avoid multiple freeze/thaw cycles.
           
          References:
          Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
          Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
          Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
          Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.

          DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 
           

          SPECIES CROSS-REACTIVITY:

          Human, mouse, rat, pig, avian, amphibian
           

          APPLICATIONS/DILUTIONS:

          IF (5-10 ug/ml)
          WB (0.5-1.0 ug/ml)
           

          SOURCE:

          Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.
           

          FORM/STORAGE:

          50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20º C.  Avoid multiple freeze/thaw cycles.
           

          References:
          Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
          Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
          Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
          Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.
           

           

          DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 
           

          SPECIES CROSS-REACTIVITY:

          Human, mouse, rat, pig, avian, amphibian
           

          APPLICATIONS/DILUTIONS:

          IF (5-10 ug/ml)
          WB (0.5-1.0 ug/ml)
           

          SOURCE:

          Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.
           

          FORM/STORAGE:

          50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20º C.  Avoid multiple freeze/thaw cycles.
           

          References:
          Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
          Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
          Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
          Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.
           

          產品咨詢

          留言框

          • 產品:

          • 您的單位:

          • 您的姓名:

          • 聯系電話:

          • 常用郵箱:

          • 省份:

          • 詳細地址:

          • 補充說明:

          • 驗證碼:

            請輸入計算結果(填寫阿拉伯數字),如:三加四=7
          上海起發實驗試劑有限公司
          地址:上海浦東川沙鎮川沙路6619號上海起發實驗試劑有限公司
          郵箱:xs1@78bio.com
          傳真:021-50724961
          關注我們
          歡迎您關注我們的微信公眾號了解更多信息:
          歡迎您關注我們的微信公眾號
          了解更多信息
          主站蜘蛛池模板: 骚虎三级在线免费播放| 国产精品粉嫩嫩在线观看| 91精品国产综合久久青草| 国内嫩模私拍精品视频| 21AV少妇导航| av中文码一区二区三区| 五月六月伊人狠狠丁香网| 久久青草国产精品一区| 久久精品国产亚洲AV麻| 亚洲AV无码精品呻吟| 日本欧美久久久久免费播放网 | 欧美一进一出抽搐大尺度视频| av网站可以直接看的| 国产免费视频| 换着玩人妻中文字幕| 国产麻豆永久视频| japanese久久中文字幕| 福利姬视频在线观看| 看免费的无码区特aa毛片| 日本怡春院欧美一区二区三区 | 亚洲中文在线精品国产| 午夜福利精品国产二区| 天天做天天爱夜夜夜爽毛片| 亚洲精品国产中文字幕| 九九热精品在线视频| 亚洲国产精品久久久天堂麻豆宅男 | 免费A级毛片无码无遮挡| 亚洲最大在线精品| 亚洲国产精品久久久久久久| 黑人巨大videos极度另类| 国产性色的免费视频网站| 最新中文字幕一区二区三区| 各种少妇wbb撒尿| 国产精品综合av一区二区国产馆 | 日韩在线播放中文字幕| 强奷乱码中文字幕熟女导航| 久久国产精品波多野结衣| 亚洲日韩中文无码久久| 亚洲精品成人久久av| 夜夜添无码一区二区三区 | 97久久超碰福利国产精品…|