MAB1692
Anti-Dystrophin Antibody, mid-rod, clone 6D3
culture supernatant, clone 6D3, Chemicon®
Sinónimos:
Anti-BMD, Anti-CMD3B, Anti-DXS142, Anti-DXS164, Anti-DXS206, Anti-DXS230, Anti-DXS239, Anti-DXS268, Anti-DXS269, Anti-DXS270, Anti-DXS272, Anti-MRX85
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Productos recomendados
biological source
mouse
Quality Level
antibody form
culture supernatant
antibody product type
primary antibodies
clone
6D3, monoclonal
species reactivity
mouse, canine, human, rabbit, rat
manufacturer/tradename
Chemicon®
technique(s)
immunohistochemistry: suitable
western blot: suitable
isotype
IgG2a
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
human ... DMD(1756)
Specificity
Mid rod domain (between amino acids 1181 and 1388) of human dystrophin. Also reacts with skeletal, cardiac and smooth muscle dystrophin from normal mouse, rat, rabbit and dog. Other animal species have not been tested. Reacts on blots with the brain isoform. No reactivity with mdx mouse tissue or DMD/BMD patients who have a gene deletion which removes the antibody binding site. Does not react with chicken dystrophin.
STAINING PATTERN:Light microscopy: continuous rim of labeling at the periphery of muscle fibers.
E.M. gold: close to the cytoplasmic face of the plasma membrane.
Western blotting: strong double bands at approximately 400 kD plus metabolites of lower molecular mass.
STAINING PATTERN:Light microscopy: continuous rim of labeling at the periphery of muscle fibers.
E.M. gold: close to the cytoplasmic face of the plasma membrane.
Western blotting: strong double bands at approximately 400 kD plus metabolites of lower molecular mass.
Immunogen
Bacterial fusion protein (Cell (1987) 51:919-928).
Epitope: mid-rod
Application
Immunohistochemistry: (fresh frozen, unfixed tissue only): use
undiluted - 1:20. Not recommended for use on paraffin embedded tissue.
EM Gold (Light fixation with 2% formaldehyde + 0.001% glutaraldehyde for 1 hour. 2.3M sucrose used as cryoprotectant.): use undiluted. 90 minute incubation at 25°C.
Western blotting: use 1:100-1:250.
Optimal working dilutions must be determined by the end user.
Protocol for Immunohistochemical use of MAB1692
1) Freeze muscle blocks in isopentane chilled in liquid nitrogen.
2) Cut 4 μm to 10 μm sections and air dry on slides coated with 0.5% gelatin containing 0.05% chrome alum.
3) Slides may be stored at -70 °C wrapped in cling film until required. If stored sections are used, allow sections to equilibrate to room temperature before unwrapping and proceeding.
4) Apply a 50 μL aliquot of primary antibody to sections (unfixed). Incubate for 1 hour at room temperature or 37°C.
5) Wash sections 3 x 10 minutes in phosphate buffered saline.
6) Apply a 50 μL aliquot of labeled second antibody. Incubate for 60 minutes at 25°C.
7) Wash sections 3 x 10 minutes in phosphate buffered saline.
8) Mount fluorescent sections in aqueous mounting media or visualize peroxidase label (DAB). Dehydrate, clean and mount peroxidase labeled sections for permanent preparations.
undiluted - 1:20. Not recommended for use on paraffin embedded tissue.
EM Gold (Light fixation with 2% formaldehyde + 0.001% glutaraldehyde for 1 hour. 2.3M sucrose used as cryoprotectant.): use undiluted. 90 minute incubation at 25°C.
Western blotting: use 1:100-1:250.
Optimal working dilutions must be determined by the end user.
Protocol for Immunohistochemical use of MAB1692
1) Freeze muscle blocks in isopentane chilled in liquid nitrogen.
2) Cut 4 μm to 10 μm sections and air dry on slides coated with 0.5% gelatin containing 0.05% chrome alum.
3) Slides may be stored at -70 °C wrapped in cling film until required. If stored sections are used, allow sections to equilibrate to room temperature before unwrapping and proceeding.
4) Apply a 50 μL aliquot of primary antibody to sections (unfixed). Incubate for 1 hour at room temperature or 37°C.
5) Wash sections 3 x 10 minutes in phosphate buffered saline.
6) Apply a 50 μL aliquot of labeled second antibody. Incubate for 60 minutes at 25°C.
7) Wash sections 3 x 10 minutes in phosphate buffered saline.
8) Mount fluorescent sections in aqueous mounting media or visualize peroxidase label (DAB). Dehydrate, clean and mount peroxidase labeled sections for permanent preparations.
Research Category
Metabolism
Metabolism
Research Sub Category
Muscle Physiology
Muscle Physiology
This Anti-Dystrophin Antibody, mid-rod, clone 6D3 is validated for use in WB, IH for the detection of Dystrophin.
Physical form
Culture supernatant, liquid in PBS with 1% BSA, containing 15 mM sodium azide.
Storage and Stability
Maintain at -20°C for up to one year in convenient undiluted aliquots. Avoid repeated freeze/thaw cycles.
Analysis Note
Control
POSITIVE CONTROL: Snap frozen normal human or rat striated muscle.
POSITIVE CONTROL: Snap frozen normal human or rat striated muscle.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
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.
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Precios
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Journal of Cell Science null
Addeli Bez Batti Angulski et al.
Scientific reports, 10(1), 10967-10967 (2020-07-06)
We sought here to induce the excision of a large intragenic segment within the intact dystrophin gene locus, with the ultimate goal to elucidate dystrophin protein function and stability in striated muscles in vivo. To this end, we implemented an
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