MABT827-AF488

Anti-Dystrophin Antibody, clone 2C6 (MANDYS106), Alexa Fluor^™ 488 Conjugate

clone 2C6 (MANDYS106), from mouse, ALEXA FLUOR^™ 488

• 同義詞: Dystrophin
• 分類程式碼代碼: 12352203
• eCl@ss: 32160702

屬性

• 生物源: mouse
• 品質等級: 100
• 共軛: ALEXA FLUOR^™ 488
• 抗體表格: purified immunoglobulin
• 抗體產品種類: primary antibodies
• 無性繁殖: 2C6 (MANDYS106), monoclonal
• 物種活性: human
• 技術: immunofluorescence: suitable
• 同型: IgG2aκ
• NCBI登錄號: NP_000100
• UniProt登錄號: P11532
• 運輸包裝: ambient
• 目標翻譯後修改: unmodified
• 基因資訊: human ... DMD(1756)

描述

一般說明

Dystrophin (UniProt P11532) is encoded by the DMD (also known as BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85) gene (Gene ID 1756) in human. Dystrophin is localized to the inner part of the muscle fiber cell membrane (sarcolemma), where it forms the dystrophin-associated glycoprotein complex (DGC) that links the extracellular matrix to the actin cytoskeleton. Dystrophin plays an important role in stabilizing the muscle fibre against the mechanical forces of muscle contraction by providing a shock-absorbing connection between the cytoskeleton and the extracellular matrix. Duchenne muscular dystrophy (DMD) is caused by gene mutations that disrupt the open reading frame (ORF) and prevent the full translation of dystrophin. ORF restoration by exon skipping using antisense oligonucleotides targeted to splicing elements are designed to transform the DMD phenotype to that of the milder disorder, Becker muscular dystrophy (BMD), typically caused by in-frame dystrophin deletions that allow the production of an internally deleted but partially functional dystrophin.

特異性

Detects dystrophin spliced isoforms 1-4, but not isoforms 5-10, or utrophin. Positive muscle membrane staining of tissue samples from healthy donors, reduced staining of Becker muscular dystrophy (BMD) biopsies, and no staining is seen with Duchenne muscular dystrophy (DMD) biopsy samples (Anthony, K., et al. (2011). Brain. 134(Pt 12):3547-3559).

免疫原

TrpE-tagged recombinant protein corresponding to the Exon 43-coded pectrin-like repeat 16 region of human Dystrophin.

應用

Research Category
Cell Structure

The unconjugated antibody (Cat. No. MABT827) and Alexa Fluor^™ 555 conjugate (Cat. No. MABT827-AF555) are also available for Immunohistochemistry, Immunofluorescence, and Western Blotting applications.

This mouse monoclonal Anti-Dystrophin Antibody, clone 2C6 (MANDYS106), Alexa Fluor^™ 488 Conjugate, Cat. No. MABT827-AF488 is validated for use in Immunofluorescence for the detection of Dystrophin.

品質

Evaluated by Immunofluorescence in human skeletal muscle tissue sections.

Immunofluorescence Analysis: A 1:25 dilution of this antibody detected dystrophin in human skeletal muscle tissue sections.

標靶描述

~427 kDa observed.

外觀

Protein G purified.

Purified mouse IgG2a Alexa Fluor^™ 488 conjugate in buffer containing PBS, 1.5% BSA with 0.05% sodium azide

儲存和穩定性

Stable for 1 year at 2-8°C from date of receipt.

其他說明

Concentration: Please refer to lot specific datasheet.

法律資訊

ALEXA FLUOR is a trademark of Life Technologies

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

安全資訊

• 儲存類別代碼: 12 - Non Combustible Liquids
• 水污染物質分類（WGK）: WGK 2
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable