Rabbit Recombinant Monoclonal DHX36 antibody. Suitable for IP, WB and reacts with Mouse samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
IP | WB | |
---|---|---|
Human | Not recommended | Not recommended |
Mouse | Tested | Tested |
Rat | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/30 | Notes Use at 1:30 dilution (2μg in 0.35mg lysates). |
Species | Dilution info | Notes |
---|---|---|
Species Human, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Rat | Dilution info - | Notes - |
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Multifunctional ATP-dependent helicase that unwinds G-quadruplex (G4) structures (PubMed:25611385). Plays a role in many biological processes such as genomic integrity, gene expression regulations and as a sensor to initiate antiviral responses (PubMed:21590736, PubMed:21703541). G4 structures correspond to helical structures containing guanine tetrads (By similarity). Binds with high affinity to and unwinds G4 structures that are formed in nucleic acids (G4-DNA and G4-RNA) (By similarity). Plays a role in genomic integrity (By similarity). Converts the G4-RNA structure present in telomerase RNA template component (TREC) into a double-stranded RNA to promote P1 helix formation that acts as a template boundary ensuring accurate reverse transcription (By similarity). Plays a role in transcriptional regulation. Resolves G4-DNA structures in promoters of genes, such as YY1, KIT/c-kit and ALPL and positively regulates their expression (By similarity) (PubMed:25611385). Plays a role in post-transcriptional regulation (By similarity). Unwinds a G4-RNA structure located in the 3'-UTR polyadenylation site of the pre-mRNA TP53 and stimulates TP53 pre-mRNA 3'-end processing in response to ultraviolet (UV)-induced DNA damage (By similarity). Binds to the precursor-microRNA-134 (pre-miR-134) terminal loop and regulates its transport into the synapto-dendritic compartment (By similarity). Involved in the pre-miR-134-dependent inhibition of target gene expression and the control of dendritic spine size (By similarity). Plays a role in the regulation of cytoplasmic mRNA translation and mRNA stability (By similarity). Binds to both G4-RNA structures and alternative non-quadruplex-forming sequence within the 3'-UTR of the PITX1 mRNA regulating negatively PITX1 protein expression (By similarity). Binds to both G4-RNA structure in the 5'-UTR and AU-rich elements (AREs) localized in the 3'-UTR of NKX2-5 mRNA to either stimulate protein translation or induce mRNA decay in an ELAVL1-dependent manner, respectively (By similarity). Binds also to ARE sequences present in several mRNAs mediating exosome-mediated 3'-5' mRNA degradation (By similarity). Involved in cytoplasmic urokinase-type plasminogen activator (uPA) mRNA decay (By similarity). Component of a multi-helicase-TICAM1 complex that acts as a cytoplasmic sensor of viral double-stranded RNA (dsRNA) and plays a role in the activation of a cascade of antiviral responses including the induction of pro-inflammatory cytokines via the adapter molecule TICAM1 (PubMed:21703541). Required for the early embryonic development and hematopoiesis (PubMed:22422825). Involved in the regulation of cardioblast differentiation and proliferation during heart development (PubMed:26489465). Involved in spermatogonia differentiation (PubMed:25611385). May play a role in ossification (PubMed:21590736).
Ddx36, Kiaa1488, Mlel1, Dhx36, ATP-dependent DNA/RNA helicase DHX36, DEAD/H box polypeptide 36, DEAH box protein 36, MLE-like protein 1, RNA helicase associated with AU-rich element ARE
Rabbit Recombinant Monoclonal DHX36 antibody. Suitable for IP, WB and reacts with Mouse samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% 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.
DHX36 also known as RHAU or G4R1 is a member of the DEAH-box family of RNA helicases. It has an estimated molecular mass of approximately 115 kDa. The protein exhibits robust expression in various tissues including the heart skeletal muscle and brain. Mechanically DHX36 plays a role in resolving RNA G-quadruplexes and DNA G-quadruplexes which are secondary structures that can form in nucleic acids. Its ability to unwind these structures is critical for the regulation of gene expression and maintenance of genomic stability.
DHX36 acts as an RNA helicase and is essential in the regulation of translation and transcription. It plays a significant role in binding G-quadruplex structures within the 5' untranslated region of mRNAs. DHX36 also forms part of larger protein complexes that regulate ribosome assembly and function. This protein helps ensure proper ribosomal RNA processing facilitating efficient protein synthesis. Through its involvement in these complexes DHX36 aids in the regulation of cellular stress responses and apoptosis.
DHX36 significantly contributes to several cellular processes notably the regulation of transcription and translation. It actively participates in the Wnt signaling pathway influencing the stability of target mRNAs. DHX36 also interacts with proteins like FTO and NPM1 that are known to be involved in mRNA processing. These interactions and pathway linkages highlight its role in controlling gene expression and cellular growth.
DHX36 has been linked to cardiac dysfunctions and neurological disorders. Its improper functioning has been associated with arrhythmias due to its role in cardiac gene expression regulation. In neurological contexts DHX36 disruptions may contribute to various cognitive disorders acting through its impact on synaptic protein synthesis. In these pathological conditions proteins such as TDP-43 and FUS are affected emphasizing the importance of DHX36 in maintaining cellular homeostasis and preventing disease progression.
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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Terms & Conditions.
DHX36 was immunoprecipitated from 0.35 mg RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate with ab223564 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab223564 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate 10ug
Lane 2: ab223564 IP in RAW 264.7 whole cell lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of ab223564 in RAW 264.7 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 3 minutes
All lanes: Immunoprecipitation - Anti-DHX36 antibody [EPR20868-12] (ab223564)
Predicted band size: 115 kDa
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time:
Lanes 1-5: 3 minutes;
Lane 6: 15 seconds.
All lanes: Western blot - Anti-DHX36 antibody [EPR20868-12] (ab223564) at 1/1000 dilution
Lane 1: Mouse testis tissue lysate at 20 µg
Lane 2: Mouse heart tissue lysate at 20 µg
Lane 3: RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate at 20 µg
Lane 4: Mouse lung tissue lysate at 20 µg
Lane 5: Mouse brain tissue lysate at 20 µg
Lane 6: NIH/3T3 (mouse embryonic fibroblast), 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 1/20000 dilution
Predicted band size: 115 kDa
Observed band size: 114 kDa
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Lysates were kindly provided by Dr Zhongzhou Yang.
ab223564 was shown to specifically react with DHX36 in wild-type mouse embryo heart tissue as signal was weaken in DHX36 knock-down tissue. Wild-type and DHX36 knock-down samples were subjected to SDS-PAGE. ab223564 and Anti-GAPDH antibody [EPR16891] - Loading Control ab181602 (Rabbit anti-GAPDH loading control) were incubated 1 hour at room temperature at 1/1000 dilution and 1/200, 000 dilution respectively. Blots were developed with Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (Goat Anti-Rabbit IgG H&L (HRP) ab97051) secondary antibody at 1/20, 000 dilution and 1/100, 000 dilution respectively for 1 hour at room temperature before imaging. The blot was developed on a BIO-RAD® ChemiDoc™ MP instrument using the ECL technique.
Exposure time: 15 seconds
All lanes: Western blot - Anti-DHX36 antibody [EPR20868-12] (ab223564) at 1/1000 dilution
Lane 1: Wild-type mouse embryo heart tissue lysate at 20 µg
Lane 2: DHX36 knock-down mouse embryo heart tissue lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Predicted band size: 115 kDa
Observed band size: 114 kDa
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