亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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  人才招聘  關于我們  聯系我們
欧美成人免费一区在线播放,久久永久免费人妻精品下载,丰满人妻一区二区三区视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-MYH7B/PE-Cy5 Conjugated antibody (bs-9862R-PE-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-9862R-PE-Cy5
英文名稱1 Rabbit Anti-MYH7B/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5標記的肌球蛋白重鏈7抗體
別    名 adult 1; Beta myosin heavy chain; cardiac muscle beta isoform; CMD1S; CMH1; MPD1; MYH1; MYH1_HUMAN; MYH7; MYH7_HUMAN; Myhc slow; MyHC-2x; MyHC-beta; MyHC-IIx/d; MyHC-slow; MYHCB; Myopathy, distal 1; Myosin heavy chain (AA 1-96); Myosin heavy chain 1; Myosin heavy chain 2x; Myosin heavy chain 7; Myosin heavy chain; Myosin heavy chain IIx/d; Myosin heavy chain slow isoform; Myosin heavy chain, cardiac muscle beta isoform; Myosin, heavy chain 7, cardiac muscle, beta; Myosin, heavy polypeptide 7, cardiac muscle, beta; Myosin-1; Myosin-7; Rhabdomyosarcoma antigen MU RMS 40.7A; skeletal muscle; SPMD.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  發育生物學  信號轉導  干細胞  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Horse, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 213kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MYH7
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:
Myosin heavy chains are ubiquitous Actin-based motor proteins that convert the chemical energy derived from ATP hydrolysis into the mechanical energy that drives diverse motile processes in eukaryotic cells, including cytokinesis, vesicular transport and cellular locomotion. Muscle myosin is a heterohexamer consisting of two myosin heavy chains and two associated nonidentical pairs of myosin light chains. The seven myosin heavy chain isoforms that predominate in mammalian skeletal muscles include two developmental isoforms, MHC-embryonic (MYH3) and MHC-perinatal (MYH8); three adult skeletal muscle isoforms, MHC IIa (MYH2), MHC IIb (MYH4) and MHC IIx/d (MYH1); and MHC-∫/slow (MYH7 or MHC-∫), which is also expressed in cardiac muscle. Research indicates that mutations of the MYH7 gene causes hypertrophic cardiomyopathy.

Function:
Muscle contraction.

Subunit:
Muscle myosin is a hexameric protein that consists of 2 heavy chain subunits (MHC), 2 alkali light chain subunits (MLC) and 2 regulatory light chain subunits (MLC-2).

Subcellular Location:
Cytoplasm, myofibril. Note=Thick filaments of the myofibrils.

DISEASE:
Defects in MYH7 are the cause of cardiomyopathy familial hypertrophic type 1 (CMH1) [MIM:192600]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
Defects in MYH7 are the cause of myopathy myosin storage (MYOMS) [MIM:608358]. In this disorder, muscle biopsy shows type 1 fiber predominance and increased interstitial fat and connective tissue. Inclusion bodies consisting of the beta cardiac myosin heavy chain are present in the majority of type 1 fibers, but not in type 2 fibers.


Similarity:
Contains 1 IQ domain.
Contains 1 myosin head-like domain.

Database links:

Entrez Gene: 58498 Human

Omim: 612147 Human

SwissProt: Q01449 Human

Unigene: 75636 Human



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.www.chomd.com.cn 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: 无码人妻少妇伦在线电影 人妻免费视频| 亚洲播放器成人av| 亚洲午夜久久久精品影院一区三区网站| 国语成本人片免费AⅤ无码| 日韩成人无码| 日产国产欧美视频一区精品| 午夜天堂精品久久久久18 | 国产成人久久久精品二区三区_亚洲伊人成 | 久久精品系列偷拍女人屁股屁股| 少妇被粗大猛烈进出免费视频下载软件| 无码人妻精品一区二区中文可达鸭 | 久久综合给合久久狠狠狠97色69|无码| 蜜芽AV网站首页入口| 久久精品一区二区三区无码图 | 在线观看免费AV网站A| 亚洲伊人久久久第一页| 久久无码中文金品站| 1204人成网站色www| 亚洲精品白浆高清久久久久久人妖怪| 亚洲第一页在线观看红桃| 韩国秘?AV无码一区二区qq群| 亚洲秘?AV无码一区二区qq群 | 肉感无码色色色不卡视频| 大 香 蕉 伊 人 在 线视频 | 中文字幕免费高清视频hh| 亚洲中文久久精品无码18禁 - 亚洲中文久久精品无码18 | 国产人成视频在线观看0| 91九色国产社区在线观看,91九色蝌蚪熟女,91 | 一区二区三区视频在线播放 | 国产亚洲一区二区在线观看99 | 亚洲大尺度无码无码专区线上免费老板| 九九九热精品免费视频观看网站| 国产三级在线观看播放视频色精屋 | 一级做a爰片久久毛片1女多男视频| 久久久久久久精品成人热色戒岬奈奈美 | 国产suv精品一区二区3d动漫| 无码国产伦一区二区三区视频al换脸| 国产成人精品AA毛片1322| 色丝袜av咪咪咪咪| 中文字幕亚洲情99在线,野花社区www视 | 欧美一区日本一区韩国一区|