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          • Primary Antibodies ›
          • Dystrophin Antibodies

          Fabgennix

          Dystrophin Polyclonal Antibody, FITC

          View all (36) Dystrophin antibodies

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          Datasheet
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          Cite Dystrophin Polyclonal Antibody, FITC

          Product Details

          DMD-FITC

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:500
          -

          ELISA (ELISA)

          1:10,000
          -

          Immunoprecipitation (IP)

          1:200
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Synthetic peptide corresponding to amino acids within region 1-50 on human Dystrophin protein.
          View immunogen

          Conjugate

          FITC FITC FITC

          Excitation/Emission Max

          498/517 nm View spectra spectra

          Form

          Liquid

          Concentration

          0.5-1.5 µg/mL

          Purification

          Antigen affinity chromatography

          Storage buffer

          proprietary buffer with 30% glycerol

          Contains

          0.01% sodium azide

          Storage conditions

          Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Store in the dark.

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          Target Information

          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.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: apodystrophin-3; apodystrophin-I; Duchenne muscular dystrophy (DMD); Dystrophin; dystrophin Dp40; dystrophin Dp71a; dystrophin Dp71ab; dystrophin Dp71b; dystrophin, muscular dystrophy; GS1-19O24.1; Muscular dystrophy Duchenne and Becker types; OTTHUMP00000215592; X-linked muscular dystrophy

          View more View less

          Gene Aliases: BMD; CMD3B; DMD; DNADMD1; Dp427; Dp71; DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272; DXSmh7; DXSmh9; dys; mdx; MRX85; pke

          View more View less

          UniProt ID: (Human) P11532, (Mouse) P11531

          View more View less

          Entrez Gene ID: (Human) 1756, (Mouse) 13405, (Rat) 24907

          View more View less

          Function(s)
          dystroglycan binding actin binding structural constituent of cytoskeleton protein binding zinc ion binding structural constituent of muscle myosin binding vinculin binding nitric-oxide synthase binding metal ion binding integrin binding PDZ domain binding protein complex binding
          Process(es)
          positive regulation of cell-matrix adhesion regulation of heart rate regulation of transcription, DNA-templated muscle organ development skeletal muscle tissue development establishment of blood-nerve barrier regulation of gene expression regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion positive regulation of neuron projection development regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion regulation of skeletal muscle contraction myotube cell development muscle attachment olfactory nerve structural organization negative regulation of peptidyl-serine phosphorylation cellular protein localization response to muscle stretch regulation of membrane potential peptide biosynthetic process cellular protein complex assembly neurotransmitter receptor metabolic process positive regulation of neuron differentiation muscle cell cellular homeostasis muscle fiber development nucleus localization cardiac muscle contraction regulation of ryanodine-sensitive calcium-release channel activity establishment of glial blood-brain barrier negative regulation of ERK1 and ERK2 cascade cardiac muscle cell action potential regulation of cellular response to growth factor stimulus regulation of voltage-gated calcium channel activity negative regulation of peptidyl-cysteine S-nitrosylation positive regulation of sodium ion transmembrane transporter activity aging cell differentiation muscle cell differentiation neuron projection morphogenesis cytoskeleton organization muscle filament sliding
          It has to be done as per old AB suggested Products section.
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