亚洲制服欧美另类-午夜激情av电影-日本高清中文字幕一区二区三区-中国欧美日韩一区二区三区-欧洲亚洲日本韩国-成人欧美激情一区二区-亚洲偷偷自拍高清

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
天天躁日日躁狠狠躁AV麻豆,好大好深别停视频视频,校花被惩罚下面放震蛋上课视频
Mouse Anti-Actin, alpha skeletal muscle/Cy5 Conjugated antibody (bsm-33308M-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bsm-33308M-Cy5
英文名稱 Mouse Anti-Actin, alpha skeletal muscle/Cy5 Conjugated antibody
中文名稱 Cy5標(biāo)記的肌動蛋白α1抗體
別    名 ACTS_HUMAN; Actin, alpha skeletal muscle; Alpha-actin-1; ACTA1; ACTA; ASMA; CFTD; CFTD1; CFTDM; MPFD; NEM1; NEM2; NEM3; Actin alpha skeletal muscle; actin, alpha 1, skeletal muscle 1; actin, alpha 1, skeletal muscle; actina; actine; aktin; alpha Actin 1; alpha skeletal muscle Actin; alpha skeletal muscle; alpha-actin; Beta cytoskeletal actin; nemaline myopathy type 3.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  發(fā)育生物學(xué)  細(xì)胞骨架  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 5F11
交叉反應(yīng) Human, Mouse, Rat, 
產(chǎn)品應(yīng)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 42kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ACTA1
亞    型 IgG
純化方法 affinity purified by Protein G
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(chǎn)品介紹 background:
The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects. [provided by RefSeq, Jul 2008]

Function:
Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.

Subunit:
Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others. Identified in a complex composed of ACTA1, COBL, GSN AND TMSB4X. Interacts with TTID. Interacts (via its C-terminus) with USP25; the interaction occurs for all USP25 isoforms but is strongest for isoform USP25min muscle differentiating cells.

Subcellular Location:
Cytoplasm, cytoskeleton.

Post-translational modifications:
Oxidation of Met-46 and Met-49 by MICALs (MICAL1, MICAL2 or MICAL3) to form methionine sulfoxide promotes actin filament depolymerization. MICAL1 and MICAL2 produce the (R)-S-oxide form. The (R)-S-oxide form is reverted by MSRB1 and MSRB2, which promote actin repolymerization.
Monomethylation at Lys-86 (K84me1) regulates actin-myosin interaction and actomyosin-dependent processes. Demethylation by ALKBH4 is required for maintaining actomyosin dynamics supporting normal cleavage furrow ingression during cytokinesis and cell migration.

DISEASE:
Nemaline myopathy 3 (NEM3) [MIM:161800]: A form of nemaline myopathy. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-like or rod-shaped structures in muscle fibers on histologic examination. Note=The disease is caused by mutations affecting the gene represented in this entry.
Myopathy, actin, congenital, with excess of thin myofilaments (MPCETM) [MIM:161800]: A congenital muscular disorder characterized at histological level by areas of sarcoplasm devoid of normal myofibrils and mitochondria, and replaced with dense masses of thin filaments. Central cores, rods, ragged red fibers and necrosis are absent. Note=The disease is caused by mutations affecting the gene represented in this entry.
Myopathy, congenital, with fiber-type disproportion (CFTD) [MIM:255310]: A genetically heterogeneous disorder in which there is relative hypotrophy of type 1 muscle fibers compared to type 2 fibers on skeletal muscle biopsy. However, these findings are not specific and can be found in many different myopathic and neuropathic conditions. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the actin family.

Database links:

Entrez Gene: 421534 Chicken

Entrez Gene: 281592 Cow

Entrez Gene: 58 Human

Entrez Gene: 11459 Mouse

Entrez Gene: 100154254 Pig

Entrez Gene: 29437 Rat

Omim: 102610 Human

SwissProt: P68139 Chicken

SwissProt: P68138 Cow

SwissProt: P68133 Human

SwissProt: P68134 Mouse

SwissProt: P68137 Pig

SwissProt: P68135 Rabbit

SwissProt: P68136 Rat

Unigene: 1288 Human

Unigene: 214950 Mouse

Unigene: 82732 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.a6308.cn 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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
亚洲国产AAA毛片无费看 | 91桃色无码国产在线观看二区 | 久久久久久久久久国产精品免费 | 国产午夜亚洲精品区 | 一级a性色生活片久久毛片 日韩欧美一中文字慕2O22 | 国产婬片Av片久久久久久 | 日韩亚洲人成网站在线播放 | 亚洲中文乱码在线观看AV | 国产日产欧产精品精品 | 国产情侣真实露脸在线 | 538在线视频一区二区视视频 | 日本花心黑人hd捆绑 | 911国产自产精品a | ww久久综合久中文字幕老太婆 | 国产亚洲欧美日韩综合综合二区 | 两口子交换真实刺激高潮 | 九九热视频精品在线观看 | 日本韩国亚洲综合日韩欧美国产 | 青草园网站在线观看 | 国产精品禁18久久久夂久 | 欧美日韩一级久久久久久免费看 | 狂躁美女大BBBBBB视频1 | 国产精品户露AV在线户外直播 | 女人让男人捅30分钟 | 亚洲AV√最新天堂版资源地址在线官网 | 亚洲999精品视频免费观看 | 九九热线有精品免费观看 | 18禁黄久久久AAA片 | 国产三级毛片视频 | 国内毛片毛片毛片毛片毛片毛片毛片毛片毛片毛片毛片毛片 | 无人视频在线观看完整版高清视频 | 黑人啊灬啊灬啊灬快灬深用口述 | 国产精品JK白丝AV网站 | 99久久精品免费看国产一区二区三区 | 内射毛片内射国产夫妻 | 成人国产精品日本在线 | 激情内射亚洲一区二区三区爱妻 | 黄软件破解版下载大全 | 国产成人精选视频在线观看不卡 | 欧美激情一区二区三区视频 | 最新国产精品自在自线发布 |