Rabbit Recombinant Monoclonal ZCCHC4 antibody. Suitable for IP, WB, Flow Cyt (Intra) and reacts with Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
IP | WB | Flow Cyt (Intra) | |
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Human | Tested | Tested | Tested |
Primates | Predicted | Predicted | Predicted |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/50 | Notes - |
Species | Dilution info | Notes |
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Species Primates | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/1000 | Notes This antibody works best on a semi-dry nitrocellulose membrane transfer system. |
Species | Dilution info | Notes |
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Species Primates | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/100 | Notes - |
Species | Dilution info | Notes |
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Species Primates | Dilution info - | Notes - |
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rRNA N6-methyltransferase that specifically methylates the adenine in position 4220 of 28S rRNA (PubMed:30531910, PubMed:31328227, PubMed:31695039, PubMed:31799605). N6-methylation of adenine(4220) in 28S rRNA is required for translation (PubMed:30531910, PubMed:31799605).
rRNA N(6)-adenosine-methyltransferase ZCCHC4, Zinc finger CCHC domain-containing protein 4, ZCCHC4
Rabbit Recombinant Monoclonal ZCCHC4 antibody. Suitable for IP, WB, Flow Cyt (Intra) and reacts with Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
ZCCHC4 also known as zinc finger CCHC-type containing 4 is a protein that functions as a methyltransferase specifically modifying mRNA by adding a methyl group at the N6 position of adenine. It has an estimated mass of approximately 66 kDa. Expression of ZCCHC4 is observed mainly in the nucleus of cells and it is found across various human tissues indicating its widespread functional importance.
The methyltransferase activity of ZCCHC4 plays an important role in post-transcriptional regulation of mRNA influencing its stability and translation efficiency. ZCCHC4 is part of a complex that also includes other proteins involved in RNA metabolism. Its function impacts gene expression by modulating the epigenetic marks on mRNA thereby altering the cellular response to different stimuli.
ZCCHC4 contributes significantly to the epitranscriptome particularly affecting the m6A RNA methylation pathway. This modification is vital for processes like RNA splicing export and degradation. ZCCHC4 interacts with related proteins such as METTL3 and METTL14 which are core components of the m6A methyltransferase complex highlighting its integration within this regulatory network.
Alterations in ZCCHC4 expression or function associate with certain cancers including liver cancer. Dysregulation of m6A modification in which ZCCHC4 is involved contributes to tumor progression and metastasis. Research has also linked ZCCHC4 to mental disorders with evidence suggesting that abnormal mRNA methylation affects neural gene expression. ZCCHC4's interactions with proteins like ALKBH5 an m6A demethylase further illustrate its involvement in the pathogenesis of these diseases.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
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Terms & Conditions.
Blocking/Dilution buffer: 5% NFDM/TBST.
This antibody works best on a semi-dry nitrocellulose membrane transfer system.
These lysates were kindly provided by Prof Chuan He; University of Chicago.
All lanes: Western blot - Anti-ZCCHC4 antibody [EPR20492] (ab211325) at 1/1000 dilution
Lane 1: Wild type HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2: ZCCHC4 knockout HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Developed using the ECL technique.
Predicted band size: 59 kDa
Observed band size: 59 kDa
Exposure time: 30s
ZCCHC4 was immunoprecipitated from 0.35 mg of HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate with ab211325 at 1/50 dilution. Western blot was performed from the immunoprecipitate using ab211325 at 1/1,000 dilution. VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366), was used for detection at 1/10,000 dilution.
Lane 1: HeLa whole cell lysate 10 μg (Input).
Lane 2: ab211325 IP in HeLa whole cell lysate.
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of ab211325 in HeLa whole cell lysate.
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 30 seconds.
This antibody works best on a semi-dry nitrocellulose membrane transfer system.
All lanes: Immunoprecipitation - Anti-ZCCHC4 antibody [EPR20492] (ab211325)
Predicted band size: 59 kDa
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized HepG2 (human liver hepatocellular carcinoma cell line) cell line labeling ZCCHC4 with ab211325 at 1/100 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution was used as the secondary antibody.
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized HeLa (human epithelial cell line from cervix adenocarcinoma) cell line labeling ZCCHC4 with ab211325 at 1/100 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution was used as the secondary antibody.
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