Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal ASH2L antibody. Carrier free. Suitable for WB, IHC-P, ICC/IF, Flow Cyt (Intra), IP and reacts with Human, Mouse, Rat samples.
View Alternative Names
Set1/Ash2 histone methyltransferase complex subunit ASH2, ASH2-like protein, Ash2l
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human testis tissue labeling ASH2L with ab314128 at 1/500 (1.01 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human testis. The section was incubated with ab314128 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse testis tissue labeling ASH2L with ab314128 at 1/1000 (0.505 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse testis. The section was incubated with ab314128 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized ES-D3 [D3] (mouse blastocyst-derived embryonic stem cell) cells labelling ASH2L with ab314128 at 1/50 (10.1 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/mL dilution (Green).
Confocal image showing nuclear staining in ES-D3 [D3] cell line. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat testis tissue labeling ASH2L with ab314128 at 1/1000 (0.505 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat testis. The section was incubated with ab314128 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized ES-D3 (mouse blastocyst-derived embryonic stem cell) cells labelling ASH2L with ab314128 at 1/500 dilution (0.1 ug)/Red (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
- IP
Supplier Data
Immunoprecipitation - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
ASH2L was immunoprecipitated from 0.35 mg ES-D3 (mouse embryonic pluripotent stem Cell) whole cell lysate with ab314128 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab314128 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Lysate was freshly made and used for Western blotting immediately to minimize protein degradation.
All lanes:
Immunoprecipitation - Anti-ASH2L antibody [EPR28054-48] (<a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a>) at 1/1000 dilution
Lane 1:
ES-D3 (mouse embryonic pluripotent stem Cell) whole cell lysate
Lane 2:
<a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a> IP in ES-D3 (mouse embryonic pluripotent stem Cell) whole cell lysate
Lane 3:
Rabbit monoclonal IgG (<a href='/en-us/products/primary-antibodies/rabbit-igg-monoclonal-epr25a-isotype-control-ab172730'>ab172730</a>) instead of <a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a> in ES-D3 whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 3s
- WB
Supplier Data
Western blot - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 15199122).
Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ASH2L antibody [EPR28054-48] (<a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a>) at 1/1000 dilution
All lanes:
K562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 65 kDa,80 kDa,36 kDa
false
Exposure time: 10s
- WB
Supplier Data
Western blot - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 15199122).
Lanes 1-6 are applied with Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/100000 and lane 7 is applied with Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Exposure time : Lanes 1-6 : 180 seconds, lane 7 : 37 seconds
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ASH2L antibody [EPR28054-48] (<a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a>) at 1/1000 dilution
Lane 1:
Mouse testis tissue lysate at 20 µg
Lane 2:
Mouse heart tissue lysate at 20 µg
Lane 3:
Mouse lung tissue lysate at 20 µg
Lane 4:
Mouse liver tissue lysate at 20 µg
Lane 5:
Rat heart tissue lysate at 20 µg
Lane 6:
Rat testis tissue lysate at 20 µg
Lane 7:
Human testis tissue lysate at 20 µg
Secondary
Lanes 1 - 6:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Lane 7:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 65 kDa,80 kDa,36 kDa
false
- WB
Supplier Data
Western blot - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ASH2L antibody [EPR28054-48] (<a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a>) at 1/1000 dilution
Lane 1:
F9 (mouse embryonal carcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
F9 transfected with siRNA specifically targeting ASH2L whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 65 kDa,80 kDa,36 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ASH2L antibody [EPR28054-48] (<a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a>) at 1/1000 dilution
Lane 1:
NIH/3T3 (mouse embryonic fibroblast) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
NIH/3T3 transfected with siRNA specifically targeting ASH2L whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 80 kDa,36 kDa
false
Exposure time: 37s
- WB
Supplier Data
Western blot - Anti-ASH2L antibody [EPR28054-48] - BSA and Azide free (AB314129)
This data was developed using ab314128, the same antibody clone in a different buffer formulation.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 15199122).
In lanes 1-3, the lysates were stored at -80℃ prior to Western Blotting. The bands beneath the target band (40 kDa) are likely to be degradation products. In lane 4, the lysate was freshly made and used for Western Blotting immediately to minimize protein degradation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ASH2L antibody [EPR28054-48] (<a href='/en-us/products/primary-antibodies/ash2l-antibody-epr28054-48-ab314128'>ab314128</a>) at 1/1000 dilution
Lanes 1 and 4:
ES-D3 (mouse embryonic pluripotent stem Cell) whole cell lysate at 20 µg
Lane 2:
F9 (mouse embryonal carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
MEF (mouse embryonic fibroblast (immortalized)) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 65 kDa,80 kDa,36 kDa
false
Exposure time: 37s
Related conjugates and formulations (1)
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Anti-ASH2L antibody [EPR28054-48]
Reactivity data
Product details
ab314129 is the carrier-free version of ab314128.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ASH2L participates in the regulation of gene expression. It acts as a core subunit of the SET/MLL family of H3K4 methyltransferases which form part of larger COMPASS-like complexes. These complexes modulate chromatin structure influencing transcriptional activation by methylating histone H3 at lysine 4. This modification is essential for the transition from transcriptional repression to activation during development and cell differentiation. ASH2L's role in these processes highlights its importance in maintaining proper gene expression patterns.
Pathways
ASH2L participates in the Wnt signaling pathway and influences the cell cycle. In the Wnt pathway ASH2L interacts with proteins such as β-catenin to modulate the transcription of target genes. It also affects the methylation status of promoters in various signaling pathways contributing to the regulation of gene expression involved in cell proliferation and differentiation. Additionally ASH2L is functionally connected to other proteins like MLL1 which shares involvement in chromatin remodeling and is important for epigenetic regulation.
Product protocols
- Visit the General protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com