HRP Anti-mH2A1 antibody [EPR9359(2)]
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(1 Publication)
Rabbit Recombinant Monoclonal mH2A1 antibody - conjugated to HRP. Suitable for WB, IHC-P and reacts with Human, Mouse samples. Cited in 1 publication.
View Alternative Names
H2AFY, MACROH2A1, Core histone macro-H2A.1, Histone macroH2A1, mH2A1, Histone H2A.y, Medulloblastoma antigen MU-MB-50.205, H2A/y
- WB
Lab
Western blot - HRP Anti-mH2A1 antibody [EPR9359(2)] (AB209320)
ab209320 was shown to recognize macroH2A.1 in wild-type HAP1 cells as signal was lost at the expected MW in H2AFY (macroH2A.1) knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and H2AFY (macroH2A.1) knockout samples were subjected to SDS-PAGE. ab209320 and ab184095 (Mouse monoclonal [mAbcam 9484] to GAPDH - Loading Control (Alexa Fluor® 680) loading control) were incubated overnight at 4°C at 1/5000 dilution and 1/1000 dilution respectively. The loading control was imaged using the Licor Odyssey CLx prior to blots being developed with ECL technique.
All lanes:
Western blot - HRP Anti-mH2A1 antibody [EPR9359(2)] (ab209320) at 1/5000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
H2AFY (macroH2A.1) knockout HAP1 whole cell lysate at 20 µg
Predicted band size: 40 kDa
Observed band size: 40 kDa
false
Exposure time: 90s
- WB
Lab
Western blot - HRP Anti-mH2A1 antibody [EPR9359(2)] (AB209320)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% milk before being incubated with ab209320 overnight at 4°C. Antibody binding was visualised using ECL development solution ab133406.
All lanes:
Western blot - HRP Anti-mH2A1 antibody [EPR9359(2)] (ab209320) at 1/5000 dilution
Lane 1:
HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate at 10 µg
Lane 2:
Western blot - HeLa whole cell lysate (<a href='/en-us/products/cell-lysates/hela-whole-cell-lysate-ab150035'>ab150035</a>) at 10 µg
Lane 3:
HEK293 (Human embryonic kidney cell line) Whole Cell Lysate at 10 µg
Predicted band size: 40 kDa
Observed band size: 40 kDa
true
Exposure time: 12min
Related conjugates and formulations (6)
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-mH2A1 antibody [EPR9359(2)]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-mH2A1 antibody [EPR9359(2)]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-mH2A1 antibody [EPR9359(2)]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-mH2A1 antibody [EPR9359(2)]
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Anti-mH2A1 antibody [EPR9359(2)]
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Anti-mH2A1 antibody [EPR9359(2)] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
MH2A1 plays significant roles in chromatin remodeling and gene expression regulation. It is part of the nucleosome replacing canonical histone H2A and influencing the accessibility of chromatin to transcriptional machinery. Through this function mH2A1 can repress or activate gene expression depending on cellular context and interacting partners. Its incorporation into chromatin is associated with the silencing of certain genomic regions such as inactive X chromosome in females with potential implications for epigenetic modifications and cellular differentiation.
Pathways
MH2A1 is notably involved in pathways regulating chromatin organization and cell differentiation. It plays a role in the Polycomb Repressive Complex 2 (PRC2) pathway affecting histone methylation and gene silencing. Furthermore mH2A1 interacts with proteins like EZH2 in PRC2 which carry out methylation at histone H3 on lysine 27. These interactions highlight mH2A1's involvement in maintaining repressive chromatin states and controlling gene expression patterns important for normal cell function.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Frontiers in neurology 13:869103 PubMed35911883
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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