Anti-MCM2 (phospho S108) antibody [EPR4121]
- RabMAb
- Recombinant
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(6 Publications)
Rabbit Recombinant Monoclonal MCM2 phospho S108 antibody. Suitable for IP, Flow Cyt, WB, ICC/IF and reacts with Mouse, Human, Rat samples. Cited in 6 publications.
View Alternative Names
BM28, CCNL1, CDCL1, KIAA0030, MCM2, DNA replication licensing factor MCM2, Minichromosome maintenance protein 2 homolog, Nuclear protein BM28
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-MCM2 (phospho S108) antibody [EPR4121] (AB109271)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HeLa (human cervical adenocarcinoma epithelial cell) cells labelling MCM2 (phospho S108) with ab109271 at 1/2000 (0.4 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 HeLa cells. The signal decreased after alkaline phosphatase treatment at 37℃ for 2h. 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 (Magenta). 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.
- Flow Cyt
Lab
Flow Cytometry - Anti-MCM2 (phospho S108) antibody [EPR4121] (AB109271)
Flow cytometric analysis of HeLa (human cervical adenocarcinoma epithelial cell) cells labelling MCM2 (phospho S108) with ab109271 at 1/80 dilution (1ug)/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, ab150077) at 1/5000 dilution was used as the secondary antibody.
- IP
Lab
Immunoprecipitation - Anti-MCM2 (phospho S108) antibody [EPR4121] (AB109271)
MCM2 (phospho S108) was immunoprecipitated from 0.35 mg RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate with ab109271 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab109271 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate, 10μg
Lane 2 : ab109271 IP in RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab109271in RAW 264.7 whole cell lysate.
All lanes:
Immunoprecipitation - Anti-MCM2 (phospho S108) antibody [EPR4121] (ab109271) at 1/1000 dilution
All lanes:
RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) 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
Observed band size: 125 kDa
false
Exposure time: 1s
- WB
Lab
Western blot - Anti-MCM2 (phospho S108) antibody [EPR4121] (AB109271)
All lanes:
Western blot - Anti-MCM2 (phospho S108) antibody [EPR4121] (ab109271) at 1/10000 dilution
Lane 1:
HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate at 15 µg
Lane 2:
HeLa whole cell lysate, Then the membrane was incubated with alkaline phosphatase at 15 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 1/20000 dilution
Observed band size: 125 kDa
false
Exposure time: 1s
- WB
Lab
Western blot - Anti-MCM2 (phospho S108) antibody [EPR4121] (AB109271)
All lanes:
Western blot - Anti-MCM2 (phospho S108) antibody [EPR4121] (ab109271) at 1/10000 dilution
Lane 1:
RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 15 µg
Lane 2:
RAW 264.7 whole cell lysate, Then the membrane was incubated with alkaline phosphatase at 15 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 1/20000 dilution
Observed band size: 125 kDa
false
Exposure time: 5s
- WB
Lab
Western blot - Anti-MCM2 (phospho S108) antibody [EPR4121] (AB109271)
All lanes:
Western blot - Anti-MCM2 (phospho S108) antibody [EPR4121] (ab109271) at 1/10000 dilution
Lane 1:
C6 (Rat glial tumor glial cell) whole cell lysate at 15 µg
Lane 2:
C6 whole cell lysate, Then the membrane was incubated with alkaline phosphatase at 15 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 1/20000 dilution
Observed band size: 125 kDa
false
Exposure time: 5s
Related conjugates and formulations (1)
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Anti-MCM2 (phospho S108) antibody [EPR4121] - 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 conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
MCM2 is part of the heterohexameric MCM complex including other proteins like MCM3 to MCM7. This complex serves as a helicase unwinding DNA to allow replication machinery access to the template strand. The activity of the MCM complex is tightly regulated to ensure that every section of genomic DNA is replicated once per cell cycle. Its proper function ensures genetic information replication accuracy and contributes to genome stability.
Pathways
MCM2 participates in essential biological processes such as the DNA replication pathway and the cell cycle regulatory pathway. The presence of MCM2 is critical for the G1/S transition phase of the cell cycle. It interacts with other proteins including CDC45 and GINS forming the active CMG helicase complex. This complex is pivotal in orchestrating the replication machinery and signaling pathway responses to ensure appropriate replication origin firing and accurate DNA synthesis.
Product protocols
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Target data
Publications (6)
Recent publications for all applications. Explore the full list and refine your search
eLife 11: PubMed36082941
2022
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Journal of Cancer 13:1958-1971 PubMed35399722
2022
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Methods in enzymology 661:53-75 PubMed34776223
2021
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Nature communications 11:3951 PubMed32769987
2020
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Chronic obstructive pulmonary diseases (Miami, Fla.) 7:151-162 PubMed32726073
2020
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Cell reports 27:1794-1808.e5 PubMed31067464
2019
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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