Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025]
- BOND RX™ Validated
- Recombinant
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Anti-Myosin heavy chain antibody [A4.1025] (ab315962) is a mouse monoclonal antibody - conjugated to Alexa Fluor® 488 - detecting myosin heavy chains 1,2,3,4,5,6,7 and 8 in Western Blot, IHC-P, IHC-Fr, ICC/IF. Suitable for Human, Mouse, Rat.
View Alternative Names
Myosin-1, Myosin heavy chain 1, Myosin heavy chain 2x, Myosin heavy chain IIx/d, MyHC-2x, MyHC-IIx/d, MYH1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labeling Myosin (MYH 1/2) with ab315962 at 1/100 (5.0 ug/ml) dilution.
Cytoplasmic staining on human skeletal muscle. The section was incubated with ab315962 for 60 mins at room temperature (shown in green). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 40 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of paraffin-embedded Human cardiac muscle tissue labeling Myosin (MYH 1/2) with ab315962 at 1/100 (5.0 ug/ml) dilution.
Cytoplasmic staining on human cardiac muscle. The section was incubated with ab315962 for 60 mins at room temperature (shown in green). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®. The immunostaining was performed on a Leica Biosystems BOND RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 40 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling Myosin (MYH 1/2) with ab315962 at 1/100 (5.0 ug/ml) dilution.
Cytoplasmic staining on mouse skeletal muscle. The section was incubated with ab315962 for 60 mins at room temperature (shown in green). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 40 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse skeletal muscle (fresh) tissue labeling Myosin (MYH 1/2) with ab315962 at 1/500 (1.0 ug/ml) dilution (Green).
Confocal image showing positive staining on mouse skeletal muscle. The nuclear counterstain was DAPI (Blue). The section was incubated with ab315962 for 60 mins at room temperature. The section was then mounted using Fluoromount®. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat skeletal muscle (fresh) tissue labeling Myosin (MYH 1/2) with ab315962 at 1/500 (1.0 ug/ml) dilution (Green).
Confocal image showing positive staining on rat skeletal muscle. The nuclear counterstain was DAPI (Blue). The section was incubated with ab315962 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling Myosin (MYH 1/2) with ab315962 at 1/100 (5.0 ug/ml) dilution.
Cytoplasmic staining on rat skeletal muscle. The section was incubated with ab315962 for 60 mins at room temperature (shown in green). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®. The immunostaining was performed on a Leica Biosystems BOND RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 40 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat liver (fresh) tissue labeling Myosin (MYH 1/2) with ab315962 at 1/500 (1.0 ug/ml) dilution (Green).
Negative control : confocal image showing no staining on rat liver (PMID : 30274168). The nuclear counterstain was DAPI (Blue). The section was incubated with ab315962 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling Myosin (MYH 1/2) with ab315962 at 1/100 (5.0 ug/ml) dilution.
Negative control : no staining on human liver. The section was incubated with ab315962 for 60 mins at room temperature (shown in green). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®. The immunostaining was performed on a Leica Biosystems BOND RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 40 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Alexa Fluor® 488 Anti-Myosin heavy chain antibody [A4.1025] (AB315962)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse liver (fresh) tissue labeling Myosin with ab315962 at 1/500 (1.0 ug/ml) dilution (Green).
Negative control : confocal image showing no staining on mouse liver (PMID : 30274168). The nuclear counterstain was DAPI (Blue). The section was incubated with ab315962 for 60 mins at room temperature. The section was then mounted using Fluoromount®. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Related conjugates and formulations (3)
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Anti-Myosin heavy chain antibody [A4.1025]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-Myosin heavy chain antibody [A4.1025]
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Anti-Myosin heavy chain antibody [A4.1025] - BSA and Azide free
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Biological function summary
Myosin interacts intricately with actin filaments to form a complex that executes muscle contraction and cell motility. Myosin heads bind to actin filaments employing ATP hydrolysis to generate motion. This protein is a fundamental component of the sarcomere the structural unit of muscle fibers and works in concert with other proteins like tropomyosin and troponin to regulate muscle contraction.
Pathways
Myosin has a significant role in the muscle contraction and cell motility pathways. Myosin and actin interaction is central to the sliding filament theory which is an essential part of the muscle contraction pathway. Myosin is also involved in non-muscle cell movement through the actin-myosin contractile ring in the process of cytokinesis. Myosin interacts with proteins such as actin and ATP in these pathways to facilitate cellular processes.
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