色色色AV免费电影,av天堂影音先锋在线,风韵犹存的熟妇出轨在线,国产精品视频一区二区三区

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
精品亚洲国产成人AV制服丝袜,国产成人久久精品激情91,中文字幕无码精品亚洲资源网久久
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Rhodopsin/RP4/RHO/Cy3 Conjugated antibody (bs-19872R-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-19872R-Cy3
英文名稱 Rabbit Anti-Rhodopsin/RP4/RHO/Cy3 Conjugated antibody
中文名稱 Cy3標記的視網膜色素變性蛋白4抗體
別    名 CSNBAD1; MGC138309; MGC138311; OPN 2; OPN2; opsd; OPSD_HUMAN; Opsin 2; opsin 2; Opsin 2 rod pigment; Opsin-2; Opsin2; Retinitis Pigmentosa 4; Retinitis pigmentosa 4 autosomal dominant; RHO; Rhodopsin; RP 4; RP4.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  神經生物學  信號轉導  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Cow, Rabbit, )
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 39kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Rhodopsin/RP4/RHO
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產品介紹 background:
Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25% of total cases, approximately 30% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq, Jul 2008]

Function:
Photoreceptor required for image-forming vision at low light intensity. Required for photoreceptor cell viability after birth. Light-induced isomerization of 11-cis to all-trans retinal triggers a conformational change leading to G-protein activation and release of all-trans retinal.

Subcellular Location:
Membrane. Synthesized in the inner segment (IS) of rod photoreceptor cells before vectorial transport to the rod outer segment (OS) photosensory cilia.

Tissue Specificity:
Rod shaped photoreceptor cells which mediates vision in dim light.

Post-translational modifications:
Phosphorylated on some or all of the serine and threonine residues present in the C-terminal region.

DISEASE:
Retinitis pigmentosa 4.
Night blindness, congenital stationary, autosomal dominant 1.

Similarity:
Belongs to the G-protein coupled receptor 1 family. Opsin subfamily.
Contains one covalently linked retinal chromophore.

Database links:

Entrez Gene: 509933 Cow

Entrez Gene: 493763 Dog

Entrez Gene: 6010 Human

Entrez Gene: 212541 Mouse

Entrez Gene: 24717 Rat

Omim: 180380 Human

SwissProt: Q95KU1 Cat

SwissProt: P28681 Chinese Hamster

SwissProt: P02699 Cow

SwissProt: P32308 Dog

SwissProt: P08100 Human

SwissProt: P15409 Mouse

SwissProt: P49912 Rabbit

SwissProt: P51489 Rat

Unigene: 247565 Human

Unigene: 2965 Mouse

Unigene: 406156 Mouse

Unigene: 92530 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.51putizi.com 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 日本丝袜脚一区二区| 一级黄色在线| 国产成人免费AV片在线观看| 精品久久久久成人码免费动漫| 午夜剧场免费无码A片| 百度搜索影音先锋香港三级片网站| 在线观看91精品国产网站| 久久国产精品亚洲欧美| 德国一级毛片| a级毛片在线观看| 一级国产视频午夜电影天堂| 精品一区二区三卡四卡网站| 极品女优在线不卡| 国产熟女露脸大叫高潮| 国产黄A三级三级三级看三级| 99re国产精品乱码一区| 亚洲日本久久久午夜精品| 国产精品无码专区在线播放| 轻轻操av| 91精品丝袜国产高跟在线一区| 岛国不卡的AV| 中文字幕一区二区三区日韩精品| 精品人妻一区| 人人爽人人爽人人片AV| 写真AV在线观看| 亚洲高清偷拍一区二区三区| 成年女人看A片免费视频| 色婷婷综合久色AⅤ五区最新| 美国一级天天操夜夜操| 亚洲AV高潮呻吟久久久一区二区| 99久久国产亚洲高清观看| 亚洲AV无码专区国产精品色欲| 人妻无码熟妇乱又伦精品视频| 无码免费高清久久| 色色免费av在线观看| 亚洲va国产va天堂va久久| 国产精品毛片无遮挡高清| 国产免费久久精品99久久| 2018中文字慕无码| 欧美freesex黑人又粗又大| 亚洲性爱娇喘在线播放|