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
好吊视频一区二区三区,成人AV在线看,91久久久久无码国产精品一区99
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-MYO5A/PE-Cy5.5 Conjugated antibody (bs-19173R-PE-Cy5.5)
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-19173R-PE-Cy5.5
英文名稱 Rabbit Anti-MYO5A/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的肌球蛋白5A抗體
別    名 Dilute myosin heavy chain; GS1; MYH12; MYO5; Myo5a; MYO5A_HUMAN; Myosin heavy chain 12; Myosin heavy polypeptide kinase; Myosin V; Myosin VA (heavy polypeptide 12 myoxin); Myosin-12; Myosin-Va; Myoxin; MYR12; non-muscle.  
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  免疫學  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, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
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 215kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MYO5A
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:
This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq, Dec 2008]

Function:
Processive actin-based motor that can move in large steps approximating the 36-nm pseudo-repeat of the actin filament. Involved in melanosome transport. May also be required for some polarization process involved in dendrite formation.

Tissue Specificity:
Detected in melanocytes.

DISEASE:
Defects in MYO5A are a cause of Griscelli syndrome type 1 (GS1) [MIM:214450]; also known as Griscelli syndrome with primary neurologic impairment. Griscelli syndrome is a rare autosomal recessive disorder that results in pigmentary dilution of the skin and hair, the presence of large clumps of pigment in hair shafts, silvery-gray hair and accumulation of melanosomes in melanocytes. GS1 patients show developmental delay, hypotonia and mental retardation, without apparent immune abnormalities.
Defects in MYO5A are a cause of Griscelli syndrome type 3 (GS3) [MIM:609227]. GS3 is characterized by pigmentary dilution of the skin and hair, the presence of large clumps of pigment in hair shafts, silvery-gray hair and accumulation of melanosomes in melanocytes, without other clinical manifestations.
Defects in MYO5A are a cause of Elejalde syndrome (ELEJAS) [MIM:256710]; also known as neuroectodermal melanolysosomal disease. Elejalde syndrome is an autosomal recessive condition characterized by skin hypopigmentation, the presence of large clumps of pigment in hair shafts, silvery-gray hair, accumulation of melanosomes in melanocytes and primary neurological abnormalities. Elejalde syndrome may be the same entity as Griscelli syndrome type 1.

Similarity:
Contains 1 dilute domain.
Contains 6 IQ domains.
Contains 1 myosin head-like domain.

Database links:

Entrez Gene: 4644 Human

Entrez Gene: 17918 Mouse

Entrez Gene: 594849 Pig

Entrez Gene: 25017 Rat

Omim: 160777 Human

SwissProt: Q02440 Chicken

SwissProt: Q9Y4I1 Human

SwissProt: Q99104 Mouse

SwissProt: Q9QYF3 Rat

Unigene: 21213 Human

Unigene: 596221 Human

Unigene: 3645 Mouse

Unigene: 44865 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: 做爱网站免费| 久久97精品久久久久久久不卡| 色图都市欧美亚洲日韩小说| 欧美精品性生活| 青青草原综合久久大伊人精品| 护士奶头又白又大又好摸视频| 精品无码国产自产拍在线观看蜜| 大尺度不打码A片在线观看| 不卡无码人妻一区三区音频| 香港伦理电影在线观看| 亚洲国产精品久久人人爱| 国产精品大白屁股XXXXX| 91视频免费看| 国产一级a毛一级a看免费软件| 天码av无码一区二区三区四区| 国产人妻人伦精品1国产| 国产精品极品美女自在线观看免费| 极品露出白嫩视频在线观看| 无遮挡色视频真人免费午夜| 国产婷婷国语对白| 特黄特黄的欧洲欧美一美篇| 影音先锋亚洲日韩女优| 91视频免费看| 七色成年激情网| 久久图库色色| 亚洲色偷偷综合亚洲av伊人| 亚洲av成人无码久久精品老人| 欧美日韩色色| 欧美性一乱一交一视一频| 香蕉国产精品麻豆| 哇嘎手机视频免费看黄片| 国产成人AV黄色大片| 欧洲一卡三卡四卡免费网站| 午夜影视在线免费观看| 欧美一区二区好的精华液| 国产精品免费视频网站| 精品国产一区二区三区不卡| 日韩精品无码不卡视频| 国产精品亚洲二区在线观看| 影音先锋日韩色色资源| 亚洲精品无码高潮喷水在线|