Merck Millipore代理MAB3430 Anti-Desmin Antibody, clone DE-B-5;抗结蛋白抗体,克隆DE-B-5store at +2℃ to +8℃

2025-06-28

货号:MAB3430

品牌:Merck Millipore

规格:40Ug

目录价:¥5359.00

市场价格:¥4555.15

会员价格:¥4287.20

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-Desmin Antibody, clone DE-B-5 | MAB3430 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Trade Name: Chemicon (Millipore) View All» Specificity: The antibody reacts with desmin from human, pig, rat and taod. In tissue sections this antibody is used to stain skeletal, cardiac, visceral, and some vascular smooth muscle cells. Cell lines such as RD (ATCC CCL 136) and hamster BHK-21 are positive (Debus et al., 1983). View All» Immunogen: Purified desmin. View All» Clone: DE-B-5 View All» Isotype: IgG1 View All» Species Reactivity:

  • Human

  • Pig

  • Rat

  • Frog

  • Mouse

    View All» Application Notes: Immunocytochemistry: (5 μg/ml) Immunohistochemistry: (5 μg/ml) See IHC2011-6 for prediluted and detailed paraffin protocols. Optimal working dilutions must be determined by end user. Immunohysto/cyto chemistry Protocols Ideal specimens are obtained from frozen sections from shock-frozen tissue samples. The frozen sections are dried in the air and then fixed with acetone at -20°C for 10 min. Excess acetone is allowed to evaporate at 15-25°C. Material fixed in alcohol and embedded in paraffin can also be used (2). Formaldehyde fixation will reduce or eliminate the intensity of staining depending on the conditions under which it is performed. Other fixation conditions must be first tested by the investigator. It is advantageous to block unspecific binding sites by overlaying the sections with fetal calf serum for 20-30 min at 15-25°C. Excess of fetal calf serum is removed by decanting before application of the antibody solution. Cytocentrifuge preparations of single cells or cell smears are also fixed in acetone. These preparations should, however not be dried in the air. Instead, the excess acetone is removed by briefly washing in phosphate-buffered saline (PBS). Further treatment is then as follows: • Overlay the preparation with 10-20 μl antibody solution and incubate in a humid chamber at 37°C for 1 h. • Dip the slide briefly in PBS and then wash 3 x in PBS for 3 min (using a fresh PBS bath in each case). • Wipe the margins of the preparation dry and overlay the preparation with 10-20 μl of a solution of anti-mouse Ig-FITC or anti-mouse IgG-peroxidase solution and allow to incubate for 1 h at 37°C in a humid chamber. • Wash the slide as described above. The preparation must not be allowed to dry out during any of the steps. If using an indirect immunofluorescence technique, the preparation should be overlaid with a suitable embedding medium (e.g. Moviol, Hoechst) and examined under the fluorescence microscope. If a POD-conjugate has been used as the secondary antibody, the preparation should be overlaid with a substrate solution (see below) and incubated at 15-25°C until a clearly visible redbrown color develops. A negative control (e.g. only the secondary antibody) should remain unchanged in color during this incubation period. Subsequently, the substrate is washed off with PBS and the preparation is stained, if desired, with hemalum stain for about 1 min. The hemalum solution is washed off with PBS; the preparation is embedded and examined. Substrate solutions: Aminoethyl-carbazole: Dissolve 2 mg 3-amino-9-ethylcarbazole with 1.2 ml dimethylsulfoxide and add 28.8 ml 50 mM Tris-HCI, pH 7.3, and 20 μl 3% H 2 O 2 (w/v). Prepare solution freshly each day. Diaminobenzidine: Dissolve 25 mg 3,3'-diaminobenzidine with 50 ml 50 mM Tris-HCI, pH 7.3, and add 40 μl 3% H 2 O 2 (w/v). Prepare solution freshly each day. View All» Quality Assurance: Western Blot Analysis: 1:1000 dilution View All» Presentation: Liquid in 0.02 M phosphate buffer, 0.25M NaCl with 0.1% sodium azide, pH 7.6. View All» Storage Conditions: Maintain antibody refrigerated at 2-8°C in undiluted aliquots for up to 6 months. DO NOT FREEZE. View All» UniProt Number: P17661 View All» Entrez Gene Number: NM_001927.3 View All» Gene Symbol:
    • DES

    • CSM2

    • FLJ41013

    • FLJ39719

    • CSM1

    • FLJ41793

    • FLJ12025

    • Desmin.

    • CMD1I

    • desmin

      View All» Usage Statement: 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. View All» Key Applications:
      • Western Blotting

      • Immunohistochemistry

      • Immunohistochemistry (Paraffin)

      • Immunohistochemistry (Paraffin)

        View All» Entrez Gene Summary: This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin-related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies. View All» UniProt Summary: FUNCTION: SwissProt: P17661 # Desmin are class-III intermediate filaments found in muscle cells. In adult striated muscle they form a fibrous network connecting myofibrils to each other and to the plasma membrane from the periphery of the Z-line structures.SIZE: 470 amino acids; 53536 Da SUBUNIT: Homopolymer.SUBCELLULAR LOCATION: Cytoplasm.DISEASE: SwissProt: P17661 # Defects in DES are the cause of desmin-related cardio- skeletal myopathy (CSM) [MIM:601419]; also known as desmin-related myopathy (DRM). CSM is characterized by skeletal muscle weakness associated with cardiac conduction blocks, arrhythmias, restrictive heart failure, and by intracytoplasmic accumulation of desmin-reactive deposits in cardiac and skeletal muscle cells. A desmin-related myopathy can have a distal onset, it is then known as hereditary distal myopathy (HDM). & Defects in DES are the cause of dilated cardiomyopathy 1I (CMD1I) [MIM:604765]. CMD1I is an autosomal form of dilated cardiomyopathy characterized by ventricular dilatation and impaired systolic function.SIMILARITY: SwissProt: P17661 ## Belongs to the intermediate filament family. View All» Brand Family: Chemicon View All» Product Name: Anti-Desmin, clone DE-B-5 View All» Concentration: 1 mg/mL View All» Antibody Type: Monoclonal Antibody View All» Qty/Pk: 40 µg View All» Target / Localization: Most muscle types and pericytes View All» Format: Purified View All» Host: Mouse View All»

        © 金山科研平台是专业的授权总代理区域代理经销平台。
        © 如需询价,请加客服QQ:1749072012 、客服微信:jinshanbio,或发送邮件到1749072012@qq.com
        © 平台为生命科学研究相关领域提供一站式耗材试剂仪器解决方案和采购服务,数据资源基于CC协议。
        © 本文地址:https://16ao.com/thread-131108.htm
        © Merck Millipore代理MAB3430 Anti-Desmin Antibody, clone DE-B-5;抗结蛋白抗体,克隆DE-B-5store at +2℃ to +8℃,产品报价联系微信jinshanbio
产品询价需求提交
产品询价请加微信:jinshanbio
返回