Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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(1 Publication)
Rabbit Recombinant Monoclonal SMYD3 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra), IHC-P and reacts with Human samples. Cited in 1 publication.
View Alternative Names
ZMYND1, ZNFN3A1, SMYD3, Histone-lysine N-methyltransferase SMYD3, SET and MYND domain-containing protein 3, Zinc finger MYND domain-containing protein 1
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 293 cells fixed in 2% paraformaldehyde labeling SMYD3 with ab183498 at 1/110 dilution and Goat anti rabbit IgG (FITC) at 1/150 dilution. Rabbit Monoclonal IgG was used as an isotype control.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human testis labeling SMYD3 with ab183498 at 1/100 dilution and HRP Polymer for Rabbit IgG. Counterstained with Hematoxylin.
Perform heat mediated antigen retrieval with EDTA buffer pH 9 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of HeLa cells fixed in 20 °C acetone labeling SMYD3 at 1/500 dilution and Goat anti rabbit IgG(Alexa Fluor® 555) at 1/200 (red). Counterstained with DAPI (blue)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle labeling SMYD3 at 1/100 dilution and HRP Polymer for Rabbit IgG. Counterstained with Hematoxylin.
Perform heat mediated antigen retrieval with EDTA buffer pH 9 before commencing with IHC staining protocol.
- IP
Supplier Data
Immunoprecipitation - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
Immunoprecipitation of HeLa cells labeling SMYD3 with ab183498 at 1/50 dilution and Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1500.
All lanes:
Immunoprecipitation - Anti-SMYD3 antibody [EPR11106(2)] - N-terminal (<a href='/en-us/products/primary-antibodies/smyd3-antibody-epr111062-n-terminal-ab183498'>ab183498</a>)
Predicted band size: 49 kDa
false
- WB
Supplier Data
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - N-terminal (<a href='/en-us/products/primary-antibodies/smyd3-antibody-epr111062-n-terminal-ab183498'>ab183498</a>) at 1/10000 dilution
Lane 1:
HeLa lysate at 20 µg
Lane 2:
293 lysate at 20 µg
Lane 3:
T47-D lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 49 kDa
false
- WB
Lab
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
Lanes 1 - 4 : Merged signal (red and green). Green - ab183498 observed at 49 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab183498 was shown to recognize SMYD3 in wild-type HAP1 cells as signal was lost at the expected MW in SMYD3 knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and SMYD3 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% Milk. ab183498 and ab8245 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - N-terminal (<a href='/en-us/products/primary-antibodies/smyd3-antibody-epr111062-n-terminal-ab183498'>ab183498</a>) at 1/1000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
SMYD3 knockout HAP1 whole cell lysate at 20 µg
Lane 3:
HeLa whole cell lysate at 20 µg
Lane 4:
MCF7 whole cell lysate at 20 µg
Predicted band size: 49 kDa
false
- WB
Lab
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab183498).
Lanes 1 - 4 : Merged signal (red and green). Green - ab183498 observed at 49 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab183498 was shown to recognize SMYD3 in wild-type HAP1 cells as signal was lost at the expected MW in SMYD3 knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and SMYD3 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% Milk. ab183498 and ab8245 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (ab250657) at 1/1000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
SMYD3 knockout HAP1 whole cell lysate at 20 µg
Lane 3:
HeLa whole cell lysate at 20 µg
Lane 4:
MCF7 whole cell lysate at 20 µg
Predicted band size: 49 kDa
false
- WB
Supplier Data
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - BSA and Azide free (AB250657)
This data was developed using ab183498, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-SMYD3 antibody [EPR11106(2)] - N-terminal (<a href='/en-us/products/primary-antibodies/smyd3-antibody-epr111062-n-terminal-ab183498'>ab183498</a>) at 1/2000 dilution
All lanes:
MCF-7 lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 49 kDa
false
Related conjugates and formulations (1)
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Anti-SMYD3 antibody [EPR11106(2)] - N-terminal
Reactivity data
Product details
ab250657 is the carrier-free version of ab183498.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
This methyltransferase regulates transcriptional activation by methylating histones. It acts as part of transcriptional coactivator complexes interacting with RNA polymerase II. SMYD3 modulates the expression of genes involved in cell proliferation and cancer progression. Additionally it interacts with proteins like Heat Shock Protein 90 (HSP90) and promotes the stabilization of substrate proteins. Its influence extends to non-histone proteins which suggests a wider impact on cellular signaling and structure.
Pathways
SMYD3 is involved in the MAPK (Mitogen-Activated Protein Kinase) signaling pathway an important regulator of cell differentiation proliferation and survival. It interacts with key proteins in this pathway such as ERK2 (Extracellular signal-regulated kinase 2) influencing cellular outcomes. SMYD3 also plays a role in the Wnt signaling pathway which is important for development and oncogenesis. This interaction with signaling pathways underlines its significant regulatory functions within the cell.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Neuroreport 33:451-462 PubMed35775321
2022
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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