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
国产精品无码免费视频二三区,亚洲成av人片在线观看无码不卡,国产熟女露脸大叫高潮
首頁 > 產品中心 > 標記一抗 > 產品信息
Mouse Anti-beta-Actin/HRP Conjugated antibody (bsm-33036M-HRP)
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/1200.00元
大包裝/詢價
產品編號 bsm-33036M-HRP
英文名稱1 Mouse Anti-beta-Actin/HRP Conjugated antibody
中文名稱 辣根過氧化物酶標記的β-肌動蛋白/β-Actin單克隆抗體(內參抗體)
別    名 Beta Actin; beta-Actin; ACTB; Actin cytoplasmic 1; Actin, beta; Beta actin; beta cytoskeletal actin;A X actin like protein; ACTB; Actin cytoplasmic 1; alpha sarcomeric Actin; Actx; Beta cytoskeletal actin; Melanoma X actin; PS1TP5BP1; ACTB_HUMAN.  
規格價格 100ul/1200元 購買        大包裝/詢價
說 明 書 100ul  
產品類型 內參抗體 
研究領域 腫瘤  細胞生物  信號轉導  細胞骨架  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 1A2
交叉反應 Human,  (predicted: Mouse, Rat, Chicken, Dog, Pig, Cow, Sheep, Fish, Guinea Pig, Hamster, Cat, )
產品應用
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 beta-Actin
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.
產品介紹 background:
Loading Control
This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, and integrity. This actin is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins. [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 mRNP granule complex, at least composed of ACTB, ACTN4, DHX9, ERG, HNRNPA1, HNRNPA2B1, HNRNPAB, HNRNPD, HNRNPL, HNRNPR, HNRNPU, HSPA1, HSPA8, IGF2BP1, ILF2, ILF3, NCBP1, NCL, PABPC1, PABPC4, PABPN1, RPLP0, RPS3, RPS3A, RPS4X, RPS8, RPS9, SYNCRIP, TROVE2, YBX1 and untranslated mRNAs. Component of the BAF complex, which includes at least actin (ACTB), ARID1A, ARID1B/BAF250, SMARCA2, SMARCA4/BRG1, ACTL6A/BAF53, ACTL6B/BAF53B, SMARCE1/BAF57 SMARCC1/BAF155, SMARCC2/BAF170, SMARCB1/SNF5/INI1, and one or more of SMARCD1/BAF60A, SMARCD2/BAF60B, or SMARCD3/BAF60C. In muscle cells, the BAF complex also contains DPF3. Found in a complex with XPO6, Ran, ACTB and PFN1. Component of the MLL5-L complex, at least composed of MLL5, STK38, PPP1CA, PPP1CB, PPP1CC, HCFC1, ACTB and OGT. Interacts with XPO6 and EMD. Interacts with ERBB2.

Subcellular Location:
Cytoplasm. cytoskeleton.

Tissue Specificity:
Ubiquitously expressed in all eukaryotic cells.

Post-translational modifications:
ISGylated.
Oxidation of Met-44 by MICALs (MICAL1, MICAL2 or MICAL3) to form methionine sulfoxide promotes actin filament depolymerization. Methionine sulfoxide is produced stereospecifically, but it is not known whether the (S)-S-oxide or the (R)-S-oxide is produced.

DISEASE:
Defects in ACTA1 are the cause of nemaline myopathy type 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-or rod-like structures in muscle fibers on histologic examination. The phenotype at histological level is variable. Some patients present areas devoid of oxidative activity containg (cores) within myofibers. Core lesions are unstructured and poorly circumscribed.
Defects in ACTA1 are a cause of myopathy 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.

Similarity:
Belongs to the actin family.

Database links:

Entrez Gene: 396526 Chicken

Entrez Gene: 60 Human

Entrez Gene: 11461 Mouse

Entrez Gene: 100009272 Rabbit

Entrez Gene: 81822 Rat

Omim: 102630 Human

SwissProt: P60706 Chicken

SwissProt: P60712 Cow

SwissProt: P60708 Horse

SwissProt: P60709 Human

SwissProt: P60710 Mouse

SwissProt: P29751 Rabbit

SwissProt: P60711 Rat

SwissProt: P60713 Sheep

Unigene: 520640 Human

Unigene: 708120 Human

Unigene: 727576 Human

Unigene: 328431 Mouse

Unigene: 391967 Mouse

Unigene: 94978 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.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: 久久噜噜噜久久92精品国产自产| 国产综合成人久久大片91,亚洲国产成人久久综 | 国产爆乳无码视频在线观看,亚洲AV无 | 日本中文字幕有码网红小辣椒白浆 | 亚洲人一二三区深喉视频集锦 | 无码国内精品久久人妻亚洲| 久久国产成人精品护士| 俺去噜噜交交也| 亚洲国产美女精品久久久久黑暗圣经| 久久这里有精品视频农村人故事情节片黄色一维片 | 狠狠色丁香婷婷久久综合3333视频 | 久久人做人爽一区二区三区_羞羞... | 午夜三级在线观看17c| 精品免费人成视频aPP| 中文无码人妻有码人妻中文字幕-亚洲精品 | 亚洲第一页在线观看红桃| 精品国产一区二区三区在线观看免费的| 大帝gav蜜桃??一区二区三区| 亚洲精成人的网站在线看| 国内精品久久影院与96| 亚洲精品中文字幕乱码三区91_欧美一级 | JIZZ丝袜壮感的老师水多| 熟妇13亚洲| 99精品国产一区二区三区与巨 | 国产免费无码一区二区军旅片 | 精品人妻码一区二区三区_ | 精品国产污污免费网站入口不用下载| 中国老人真实写照,看完泪奔!| 日产精品99久久久久久久玉蒲团| 99久久精品国产麻豆婷婷91| 强?乳喷自慰爽无尽久久久| 91精品国产色综合久久不8男同 | 亚洲精品无码自拍九色窝| 国产三级A三级三级Gif动态图 | 乱亲女H秽乱长久久久嫂子全文| 18禁无遮拦无码国产在线播放w| 人妻无码久久中文字幕专区亚州天堂 | 国产自啪精品视频网站丝袜app| 亚洲高清一本道无码DVD在线播放 亚洲高清一本道在线看 | 亚洲www啪成人一区二区麻豆| 大又大又粗又硬又爽少妇毛片,人妻 |