mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

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(lián)系我們
日本精品电影大全一区二区,亚洲欧美日韩另类自拍,欧美日韩视频一区三区二区在线观看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Nesprin 1/BF488 Conjugated antibody (bs-19207R-BF488)
訂購熱線:400-901-9800
訂購郵箱:sales@m.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@m.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-19207R-BF488
英文名稱1 Rabbit Anti-Nesprin 1/BF488 Conjugated antibody
中文名稱 BF488標記的突觸核膜蛋白1抗體
別    名 CPG2; Enaptin; Myne-1; MYNE1; Myocyte nuclear envelope protein 1; Nesprin-1; Nuclear envelope spectrin repeat protein 1; SCAR8; Synaptic nuclear envelope protein 1; Syne-1; SYNE1; SYNE1_HUMAN; SYNE1B.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  細胞生物  神經(jīng)生物學  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Cow, Horse, 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 1010kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Nesprin 1
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 encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

Function:
Multi-isomeric modular protein which forms a linking network between organelles and the actin cytoskeleton to maintain the subcellular spatial organization. Component of SUN-protein-containing multivariate complexes also called LINC complexes which link the nucleoskeleton and cytoskeleton by providing versatile outer nuclear membrane attachment sites for cytoskeletal filaments. Involved in the maintenance of nuclear organization and structural integrity. Connects nuclei to the cytoskeleton by interacting with the nuclear envelope and with F-actin in the cytoplasm. Required for centrosome migration to the apical cell surface during early ciliogenesis.

Subcellular Location:
Nucleus outer membrane. Cytoplasm, cytoskeleton. Cytoplasm, myofibril, sarcomere. The largest part of the protein is cytoplasmic, while its C-terminal part is associated with the nuclear envelope, most probably the outer nuclear membrane. In skeletal and smooth muscles, a significant amount is found in the sarcomeres.

Tissue Specificity:
Widely expressed. Highly expressed in skeletal and smooth muscles, heart, spleen, and peripheral blood leukocytes.

DISEASE:
Defects in SYNE1 are the cause of spinocerebellar ataxia autosomal recessive type 8 (SCAR8) [MIM:610743]; also known as autosomal recessive cerebellar ataxia type 1 (ARCA1) or recessive ataxia of Beauce. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR8 is an autosomal recessive form.
Defects in SYNE1 are the cause of Emery-Dreifuss muscular dystrophy type 4 (EDMD4) [MIM:612998]. A degenerative myopathy characterized by weakness and atrophy of muscle without involvement of the nervous system, early contractures of the elbows, Achilles tendons and spine, and cardiomyopathy associated with cardiac conduction defects.

Similarity:
Belongs to the nesprin family.
Contains 1 actin-binding domain.
Contains 2 CH (calponin-homology) domains.
Contains 12 HAT repeats.
Contains 1 KASH domain.
Contains 31 spectrin repeats.

Database links:

Entrez Gene: 23345 Human

Entrez Gene: 64009 Mouse

Entrez Gene: 499010 Rat

Omim: 608441 Human

SwissProt: Q8NF91 Human

SwissProt: Q6ZWR6 Mouse

Unigene: 12967 Human

Unigene: 331626 Mouse



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.m.p2b3.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(yī)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(wǎng)安備110107000727號
日韩码一码二码三码区别| 亚洲欧美日韩国产精品专区| 欧美老熟女多毛茸茸| 中文字幕av不卡一区| 国产h视频在线播放| 精品久久久久一区二区三| 国产亚洲欧美另类网爆在线| 欧美日本一道本一区二区三区| 中文字幕无码aⅴ免费不卡| 亚洲精品夜夜夜妓女网| 日本阿v不卡在线观看视频| 亚洲AV永久无码精品加勒比| 亚洲影视一区二区三区| 亚洲av久久一区二区| av网址在线播放大全| 五月婷婷六月丁香综合小说| 国产永久免费观看的黄网站| 丰满少妇高潮一区二区| 亚洲另类欧美在线中文字幕不卡| 无码人妻视频一区二区三区| 国产盗摄视频在线播放| 亚洲欧美成人久久一区二区三区| 亚洲欧美另类色视频| 一区二区日韩av激情| 国产精品女同久久久久久| 国产精品熟女高潮久久99| 尤物亚洲综合色区另类aⅴ| 日韩一区二区三区日韩精品| 18禁久久久久久久久久久久久久| 激情小说校园春色亚洲| 九色九九综合久久爱| 亚洲Av无码精品色午夜蜜芽| 欧美一区二区三区啪啪| 在线精品国产一区二区三区| 99久久免费精品国产免费高清| 亚洲欧美一区二区久久| 亚洲日韩欧美制服第一页| 在线视频精品福利91| 一区二区三区四区欧美日韩亚洲| 国产精品国语对白在线观看| 91香蕉下载并安装|