Rabbit Recombinant Monoclonal PUS10 antibody. Carrier free. Suitable for WB, IP, Flow Cyt (Intra), IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
WB | IP | Flow Cyt (Intra) | IHC-P | ICC/IF | |
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Human | Tested | Tested | Tested | Tested | Not recommended |
Mouse | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Rat | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human, Mouse, Rat | Dilution info - | Notes - |
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Protein with different functions depending on its subcellular location: involved in miRNA processing in the nucleus and acts as a tRNA pseudouridylate synthase in the cytoplasm (PubMed:31819270, PubMed:33023933). In the cytoplasm, acts as a pseudouridylate synthase by catalyzing synthesis of pseudouridine(54) and pseudouridine(55) from uracil-54 and uracil-55, respectively, in the psi GC loop of a subset of tRNAs (PubMed:30530625, PubMed:31819270, PubMed:33023933). tRNA pseudouridylate synthase activity is enhanced by the presence of 1-methyladenosine at position 53-61 of tRNAs (PubMed:30530625). Does not show tRNA pseudouridylate synthase activity in the nucleus (PubMed:33023933). In the nucleus, promotes primary microRNAs (pri-miRNAs) processing independently of its RNA pseudouridylate synthase activity (PubMed:31819270). Binds pri-miRNAs (PubMed:31819270). Modulator of TRAIL/TNFSF10-induced cell death via activation of procaspase-8 and BID cleavage (PubMed:14527409, PubMed:19712588). Required for the progression of the apoptotic signal through intrinsic mitochondrial cell death (PubMed:19712588).
CCDC139, DOBI, PUS10, tRNA pseudouridine synthase Pus10, Hup10, Coiled-coil domain-containing protein 139, tRNA pseudouridine 55 synthase, tRNA pseudouridylate synthase, tRNA-uridine isomerase, Psi55 synthase
Rabbit Recombinant Monoclonal PUS10 antibody. Carrier free. Suitable for WB, IP, Flow Cyt (Intra), IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
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.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
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.
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.
The protein PUS10 also known as pseudouridylate synthase 10 catalyzes the isomerization of uridine to pseudouridine in RNA molecules. This process introduces pseudouridine modifications critical for RNA stability and processing. PUS10 has a molecular mass of approximately 57 kDa and it is expressed in several tissues including the heart and skeletal muscle. This protein is found in both the nucleus and cytoplasm of cells suggesting its role in modifying different types of RNA.
PUS10 plays significant functions that affect RNA biogenesis and stability. Its involvement in pseudouridylation impacts the structure and function of tRNA rRNA and other small RNA species. This protein is not part of a larger protein complex but works independently. Its activity influences the integrity of RNA molecules which is important for accurate protein synthesis and cellular function.
PUS10 significantly contributes to RNA modification and processing pathways. It is a part of the wider RNA maturation process where it cooperates with other RNA-modifying enzymes like dyskerin (DKC1). DKC1 also participates in pseudouridylation highlighting the interconnected roles in ensuring RNA’s proper folding and functionality. PUS10’s involvement in the RNA modification pathway underlines its importance in maintaining RNA function integrity.
PUS10 has been linked to several health conditions. It has notable associations with cancer and autoimmune diseases. In cancer alterations in PUS10 expression levels can disrupt normal cell function potentially leading to tumorigenesis. It also interacts with the p53 protein which plays a role in tumor suppression. In autoimmune diseases the misregulation of RNA modifications including pseudouridylation by PUS10 might contribute to autoimmune responses due to altered RNA structures. Understanding PUS10 in these contexts provides insight into how RNA modifications could influence disease progression and treatment.
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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This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
PUS10 was immunoprecipitated from 0.35 mg PC-3 (human prostate adenocarcinoma epithelial cell) whole cell lysate with Anti-PUS10 antibody [EPR26272-66] ab313622 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-PUS10 antibody [EPR26272-66] ab313622 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: PC-3 (human prostate adenocarcinoma epithelial cell) whole cell lysate
Lane 2: Anti-PUS10 antibody [EPR26272-66] ab313622 IP in PC-3 (human prostate adenocarcinoma epithelial cell) whole cell lysate
Lane 3:Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-PUS10 antibody [EPR26272-66] ab313622 in PC-3 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 24 seconds
All lanes: Immunoprecipitation - Anti-PUS10 antibody [EPR26272-66] (Anti-PUS10 antibody [EPR26272-66] ab313622) at 1/30 dilution
All lanes: PC-3 (human prostate adenocarcinoma epithelial cell) whole cell lysate
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/1000 dilution
Exposure time: 24s
This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The identity of the lower MW band at approximately 37 kDa is unknown.
Exposure time: 180 seconds
All lanes: Western blot - Anti-PUS10 antibody [EPR26272-66] (Anti-PUS10 antibody [EPR26272-66] ab313622) at 1/1000 dilution
Lane 1: Human testis tissue lysate at 20 µg
Lane 2: Human kidney tissue lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 60 kDa
Exposure time: 180s
This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time: 180 seconds
All lanes: Western blot - Anti-PUS10 antibody [EPR26272-66] (Anti-PUS10 antibody [EPR26272-66] ab313622) at 1/1000 dilution
Lane 1: 293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 2: HepG2 (human hepatocellar carcinoma epithelial cell) 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
Observed band size: 60 kDa
Exposure time: 180s
This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
In Western blot, anti-GAPDH antibody (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) loading control staining at 1/200000 dilution.
Exposure time: 103 seconds
All lanes: Western blot - Anti-PUS10 antibody [EPR26272-66] (Anti-PUS10 antibody [EPR26272-66] ab313622) at 1/1000 dilution
Lane 1: HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2: PC-3 (human prostate adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 3: PC-3 transfected with siRNA specifically targeti PUS10 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
Observed band size: 60 kDa
Exposure time: 103s
This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of PC-3 (human prostate adenocarcinoma epithelial cell) cells labelling PUS10 with Anti-PUS10 antibody [EPR26272-66] ab313622 at 1/500 dilution (0.1 ug)/Red compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control 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, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 1/5000 dilution was used as the secondary antibody.
This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human hepatocellular tissue labeling PUS10 with Anti-PUS10 antibody [EPR26272-66] ab313622 at 1/2000 (0.252 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining on human hepatocellular carcinoma. The section was incubated with Anti-PUS10 antibody [EPR26272-66] ab313622 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 Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon carcinom tissue labeling PUS10 with Anti-PUS10 antibody [EPR26272-66] ab313622 at 1/2000 (0.252 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining on human colon carcinoma. The section was incubated with Anti-PUS10 antibody [EPR26272-66] ab313622 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 Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
This data was developed using Anti-PUS10 antibody [EPR26272-66] ab313622, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling PUS10 with Anti-PUS10 antibody [EPR26272-66] ab313622 at 1/2000 (0.252 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining on human kidney. The section was incubated with Anti-PUS10 antibody [EPR26272-66] ab313622 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 Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
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