Scientific images may be resized, cropped, or adjusted for brightness or contrast for presentation purposes. These updates are limited to presentation and do not affect the underlying scientific interpretation of the data. Where available, additional source data may be provided upon request.
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Accession # P13533
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human MYH6 Antibody (940344)
MYH6 in Human Heart.
MYH6 was detected in immersion fixed paraffin-embedded sections of human heart using Mouse Anti-Human MYH6 Monoclonal Antibody (Catalog # MAB8979) at 5 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Mouse HRP-DAB Cell & Tissue Staining Kit (brown; CTS002) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm of cardiomyocytes. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.MYH6 in BG01V Human Embryonic Stem Cells.
MYH6 was detected in immersion fixed BG01V human embryonic stem cells differentiated into cardiomyocytes using Mouse Anti-Human MYH6 Monoclonal Antibody (Catalog # MAB8979) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; NL007) and counterstained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for Fluorescent ICC Staining of Stem Cells on Coverslips.Detection of Human MYH6 by Western Blot.
Western blot shows lysates of human heart atrium. PVDF membrane was probed with 2 µg/mL of Mouse Anti-Human MYH6 Monoclonal Antibody (Catalog # MAB8979) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF018). A specific band was detected for MYH6 at approximately 230 kDa (as indicated). This experiment was conducted under reducing conditions and using Western Blot Buffer Group 1.Detection of aca2xvxrfugv1hkppchb.jpg by Immunohistochemistry
ACTN2 accumulation and defective F-ACTIN polymerization during the nascent myofibril stage in UNC45B−/−-CMs(A and B) Representative IF images of MYH6, MYH10, and TTN-C in non-replated WT-CMs and UNC45B−/−-CMs harvested at day 7 or day 10. Cells were stained for (A) MYH6 and MYH10 and (B) TTN-C and MYH6. To improve visualization of MYH6 signal in the UNC45B−/− cells, additional sets of MYH6 images with a longer exposure time are shown. Scale bars: 10 μm.(C) Representative IF images of non-replated WT-CMs and UNC45B−/−-CMs harvested at day 7 or day 10 and stained for TTN-N and ACTN2. Scale bars: 10 μm.(D) Quantification results for ACTN2 signal intensity in WT-CMs and UNC45B−/−-CMs at day 7, showing ACTN2 accumulation (n = 150). Error bars represent SD. Statistical significance is indicated: ∗∗∗p < 0.001.(E and F) Left panel: representative IF images of WT-CMs and UNC45B−/−-CMs harvested at (E) day 7 and (F) day 10 and stained for ACTN2 and F-ACTIN. Scale bars: 10 μm. Results represent data from at least three independent experiments.See also Figure S3. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37295424), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of cqbumwuxr5qxaj4pkse2.jpg by Immunocytochemistry/ Immunofluorescence
Effect of ectopic UNC45B expression in WT-CMs and UNC45B−/−:-CMs(A) Western blots of the protein expression levels of UNC45B in WT-CMs, WTUNC45B-OE-CMs, and UNC45B−/−:OE-CMs. Exogenous and endogenous UNC45B are indicated.(B) Representative TEM images of WT-CMs and UNC45B−/−:OE-CMs. Scale bars are indicated.(C) Representative IF images of replated WT-CMs and WTUNC45B-OE-CMs harvested at day 30 and stained for the ACTN2 and TNNT2 (upper panel) or for MYH6 and F-ACTIN (bottom panel). Scale bars: 10 μm. Results represent data from at least three independent experiments. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37295424), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human MYH6 Antibody (940344)
Immunocytochemistry
Sample: Immersion fixed BG01V human embryonic stem cells differentiated into cardiomyocytes
Immunohistochemistry
Sample: Immersion fixed paraffin-embedded sections of human heart
Western Blot
Sample: Human heart (atrium) tissue
Reviewed Applications
Read 2 reviews rated 4.5 using MAB8979 in the following applications:
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: MYH6
Long Name
Alternate Names
Gene Symbol
UniProt
Additional MYH6 Products
Product Documents for Human MYH6 Antibody (940344)
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Human MYH6 Antibody (940344)
For research use only
Related Research Areas
Citations for Human MYH6 Antibody (940344)
Customer Reviews for Human MYH6 Antibody (940344) (2)
Have you used Human MYH6 Antibody (940344)?
Submit a review and receive an Amazon gift card!
$25/€18/£15/$25CAN/¥2500 for a review with an image
$10/€7/£6/$10CAN/¥1110 for a review without an image
Submit a review
Customer Images
-
Application: ImmunohistochemistrySample Tested: Pancreas carcinomaSpecies: HumanVerified Customer | Posted 11/18/2021
-
Application: Immunocytochemistry/ImmunofluorescenceSample Tested: hiPSC-derived cardiomyocytesSpecies: HumanVerified Customer | Posted 02/26/2019This antibody was diluted 1:50 (10ug/ml) and used for IF staining of human iPSC - derived cardiomyocytes (15 days after initiation of differentiation).
There are no reviews that match your criteria.
Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars