产品简要
公司名称 :
赛默飞世尔
其他品牌 :
NeoMarkers, Lab Vision, Endogen, Pierce, BioSource International, Zymed Laboratories, Caltag, Molecular Probes, Research Genetics, Life Technologies, Applied Biosystems, GIBCO BRL, ABgene, Dynal, Affinity BioReagents, Nunc, Invitrogen, NatuTec, Oxoid, Richard-Allan Scientific, Arcturus, Perseptive Biosystems, Proxeon, eBioscience
产品类型 :
抗体
产品名称 :
抗肌萎缩蛋白多克隆抗体
目录 :
PA5-16734
规格 :
500微升
价格 :
美国436.00
克隆性 :
多克隆
宿主 :
domestic rabbit
共轭标签 :
未共轭
反应物种 :
人类, 小鼠, 大鼠
应用 :
免疫组化, 免疫组化-石蜡切片
更多信息或购买 :
赛默飞世尔 产品网页
文章摘录数: 8
出版应用/物种/样本/稀释参考文献
  • 免疫组化; 小鼠; 图 1
Ryan T, Schmidt C, Green T, Spangenburg E, Neufer P, McClung J. Targeted Expression of Catalase to Mitochondria Protects Against Ischemic Myopathy in High-Fat Diet-Fed Mice. Diabetes. 2016;65:2553-68 pubmed 出版商
Wellmann K, Kim J, Urso P, Smith Z, Johnson B. Evaluation of vitamin A status on myogenic gene expression and muscle fiber characteristics. J Anim Sci. 2021;99: pubmed 出版商
Iyer S, Xu S, Shah S, Lovering R. Muscle phenotype of a rat model of Duchenne muscular dystrophy. Muscle Nerve. 2020;62:757-761 pubmed 出版商
Klimczak A, Zimna A, Malcher A, Kozlowska U, Futoma K, Czarnota J, et al. Co-Transplantation of Bone Marrow-MSCs and Myogenic Stem/Progenitor Cells from Adult Donors Improves Muscle Function of Patients with Duchenne Muscular Dystrophy. Cells. 2020;9: pubmed 出版商
Lee J. A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report. Ann Indian Acad Neurol. 2020;23:123-125 pubmed 出版商
Romero M, Mobley C, Mumford P, Roberson P, Haun C, Kephart W, et al. Acute and chronic resistance training downregulates select LINE-1 retrotransposon activity markers in human skeletal muscle. Am J Physiol Cell Physiol. 2018;314:C379-C388 pubmed 出版商
Vulin A, Wein N, Simmons T, Rutherford A, Findlay A, Yurkoski J, et al. The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development. Neuromuscul Disord. 2015;25:827-34 pubmed 出版商
Pratt S, Shah S, Ward C, Kerr J, Stains J, Lovering R. Recovery of altered neuromuscular junction morphology and muscle function in mdx mice after injury. Cell Mol Life Sci. 2015;72:153-64 pubmed 出版商
图像
图像 1 :
赛默飞世尔 PA5-16734 图像 1
Formalin-fixed, paraffin-embedded human skeletal muscle stained with Dystrophin antibody using peroxidase-conjugate and AEC chromogen. Note cell membrane staining of muscle fibers.
产品信息
产品类型 :
抗体
产品名称 :
抗肌萎缩蛋白多克隆抗体
目录# :
PA5-16734
规格 :
500微升
价格 :
美国436.00
克隆性 :
多克隆
纯度 :
纯化
宿主 :
兔
反应物种 :
人类, 大鼠
应用 :
免疫组化(石蜡): 1:200-1:400
物种 :
人类, 大鼠
抗体亚型 :
IgG
储存 :
4° C
描述 :
Dystrophin is the 427kDa protein product of the DMB/BMD gene located on the X chromosome at position Xp21. Western blotting and immunohistochemistry are the two established methods for the detection of abnormalities of dystrophin expression in muscle biopsies. Dystrophin abnormalities are thought to occur in 100% of patients with DMD/BMD, although genetic abnormalities may only be detected in up to 65% of cases.
免疫原 :
A合成多肽对应于C末端人的抗肌萎缩蛋白
格式 :
液体
应用w/稀释 :
免疫组化(石蜡): 1:200-1:400
别名 :
apodystrophin-3; apodystrophin-I; BMD; CMD3B; dmd; dmd.1; dmd.1.L; DNADMD1; Dp427; Dp71; Duchenne muscular dystrophy (DMD); DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272; DXSmh7; DXSmh9; dys; Dystrophin; dystrophin Dp40; dystrophin Dp71 isoform; dystrophin Dp71a; dystrophin Dp71ab; dystrophin Dp71b; dystrophin, gene 1 L homeolog; dystrophin, muscular dystrophy; GS1-19O24.1; mdx; MRX85; Muscular dystrophy Duchenne and Becker types; OTTHUMP00000215592; pke; utrn; utrophin; XELAEV_18012903mg; X-linked muscular dystrophy
更多信息或购买 :
赛默飞世尔 产品网页
公司信息
赛默飞世尔
上海浦东新金桥路27号7号楼
analyze.cn@thermofisher.com
http://www.thermo.com.cn
1084193588
公司总部: 美国