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
成人无码?Ⅴ久久精品国产传媒,日韩精品久久久久久久电影蜜臀,欧美性爱偷偷操
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-MYO5A/PE-Cy7 Conjugated antibody (bs-19173R-PE-Cy7)
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-Cy7
英文名稱 Rabbit Anti-MYO5A/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7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: 亚洲欧美强奸乱伦| 国产无套内射又大又猛又粗又爽| 国产AV一线二线三线无码| 黑人巨大精品欧美一区二区| 欧美色精品人妻在线视频| 人妻无码久久一区二区三区免费| 被黑人扒开双腿猛进| 亚洲av无码一区二区乱子伦| 国产写真免费在线观看| 欧美男人亚洲天堂欧美一区二区激情片| 成人黄色生活电影在线观看| 国产一级做A爱片久久毛片A| 最新岛国女优无码视频在线播放| 日韩人妻无码精品专区| 亚洲美女婷婷爱爱| 后入大白屁股抹油在线观看一区二区pron| 久久精品水蜜桃av综合天堂| jzzijzzij亚洲乱熟无码| 大尺度不打码A片在线观看| 国产精品 流水| 99久久夜色精品国产网站| 国产精品日韩剧情欧美| 国产偷v国产偷v亚洲高清| 亚洲日韩国产av中文字幕| 精品一精品国产一级真人片| 亚洲欧美日韩中文字幕一区二区三| chinese乱子伦xxxx国语对白| 久久久久99精品国产片| 真人黄网站亚洲欧美日韩| www.色色色色色色色网站| 麻豆国产原创最新在线视频| 人妻系列无码专区久久五月天| 影音先锋 亚洲国产| 51视频无码一区二区三区 美国大吊操大逼| 99久久精品毛片免费播放高潮又有悠悠视频| 亚洲日本中文字幕天堂网| 国产一在线精品一区在线观看| a阿v天堂免费无码专区| 影音资源aⅴ葵| www天堂网av| 久草在现三级|