Rabbit Recombinant Monoclonal RPS8 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples.
pH: 7.2 - 7.4
Constituents: PBS
ICC/IF | IP | WB | Flow Cyt (Intra) | |
---|---|---|---|---|
Human | Tested | Tested | Tested | Tested |
Mouse | Expected | Expected | Tested | Expected |
Rat | Expected | Expected | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Component of the small ribosomal subunit (PubMed:23636399). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:23636399). Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome (PubMed:34516797).
OK/SW-cl.83, RPS8, Small ribosomal subunit protein eS8, 40S ribosomal protein S8
Rabbit Recombinant Monoclonal RPS8 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples.
pH: 7.2 - 7.4
Constituents: PBS
ab251342 is the carrier-free version of Anti-RPS8 antibody [EPR17334] ab201454.
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.
Ribosomal protein S8 (RPS8) also known as S8 is a component of the small 40S subunit of the eukaryotic ribosome. This protein has a mass of approximately 20 kDa and is widely expressed in most tissues reflecting its fundamental role in cellular processes. RPS8 belongs to the ribosomal protein S8P family and plays a mechanical role in the assembly and function of the ribosome where it contributes to protein synthesis by facilitating mRNA translation.
Ribosomal protein S8 is fundamental in translation an essential cellular process that translates mRNA sequences into polypeptide chains. As part of the ribosomal 40S subunit RPS8 aids in the initiation of translation by interacting with other ribosomal proteins and rRNA to form a functional ribosome. This subunit along with the 60S large subunit comprises the active ribosome complex engaged in translating genetic information into the proteome.
RPS8 is involved in the protein synthesis pathway a critical driver of cellular proliferation and metabolism. It participates actively in the mRNA surveillance pathway ensuring the efficiency and accuracy of translation. It interacts with other proteins such as RPS6 and RPS14 which are also constituents of the small ribosomal subunit acting synergistically to regulate the efficacy of the translation process. Moreover RPS8 involvement in the ribosome biogenesis pathway emphasizes its integral role in cellular growth and division.
Alterations in ribosomal protein S8 are connected to ribosomopathies a group of disorders characterized by defective ribosome function. Dysregulation or mutations in RPS8 can lead to Diamond-Blackfan anemia a rare congenital disorder causing impaired erythropoiesis. Additionally RPS8 has correlations with cancer where aberrant expression levels contribute to tumorigenesis. In cancer RPS8 might interact with oncogenic proteins such as MYC heightening the proliferative potential of cancer cells.
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.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-RPS8 antibody [EPR17334] ab201454, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-RPS8 antibody [EPR17334] (Anti-RPS8 antibody [EPR17334] ab201454) at 1/10000 dilution
Lane 1: Jurkat (Human T cell leukemia cells from peripheral blood) whole cell lysate at 20 µg
Lane 2: HEK293 (Human embryonic kidney) whole cell lysate at 20 µg
Lane 3: A549 (Human lung carcinoma) whole cell lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 24 kDa
Observed band size: 24 kDa
Exposure time: 10s
This data was developed using Anti-RPS8 antibody [EPR17334] ab201454, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-RPS8 antibody [EPR17334] (Anti-RPS8 antibody [EPR17334] ab201454) at 1/10000 dilution
Lane 1: Human cerebellum lysate at 10 µg
Lane 2: Human pancreas lysate at 10 µg
All lanes: Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 24 kDa
Observed band size: 24 kDa
Exposure time: 10s
This data was developed using Anti-RPS8 antibody [EPR17334] ab201454, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-RPS8 antibody [EPR17334] (Anti-RPS8 antibody [EPR17334] ab201454) at 1/2000 dilution
Lane 1: C6 (Rat glial tumor cells) whole cell lysate at 10 µg
Lane 2: RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) whole cell lysate at 10 µg
Lane 3: PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysate at 10 µg
All lanes: Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 24 kDa
Observed band size: 24 kDa
Exposure time: 10s
This data was developed using Anti-RPS8 antibody [EPR17334] ab201454, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton-X100 permeabilized A549 (Human lung carcinoma) cells labeling RPS8 with Anti-RPS8 antibody [EPR17334] ab201454 at 1/600 dilution, followed by AlexaFluor®488 Goat anti-Rabbit secondary antibody (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/500 dilution (green). Confocal image showing cytoplasmic staining on A549 cell line. The nuclear counter stain is DAPI (blue). Tubulin is stained with Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 anti-Tubulin (mouse mAb) at 1/1000 dilution, followed by AlexaFluor®594 Goat anti-Mouse secondary antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at 1/500 dilution (red).
-ve control 1: Anti-RPS8 antibody [EPR17334] ab201454 at 1/600 dilution followed by AlexaFluor®594 Goat anti-Mouse secondary antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at 1/500 dilution.
-ve control 2: Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 anti-Tubulin (mouse mAb) at 1/1000 dilution, followed by AlexaFluor®488 Goat anti-Rabbit secondary antibody (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/500 dilution.
This data was developed using Anti-RPS8 antibody [EPR17334] ab201454, the same antibody clone in a different buffer formulation.RPS8 was immunoprecipitated from 1mg of HEK293 (Human embryonic kidney) whole cell lysate with Anti-RPS8 antibody [EPR17334] ab201454 at 1/50 dilution. Western blot was performed from the immunoprecipitate using Anti-RPS8 antibody [EPR17334] ab201454 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) was used for detection at 1/1500 dilution. Lane 1: HEK293 whole cell lysate 10 µg (Input). Lane 2: Anti-RPS8 antibody [EPR17334] ab201454 IP in HEK293 whole cell lysate. Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-RPS8 antibody [EPR17334] ab201454 in HEK293 whole cell lysate. Blocking and dilution buffer and concentration: 5% NFDM/TBST. Exposure time: 10 seconds.
All lanes: Immunoprecipitation - Anti-RPS8 antibody [EPR17334] (Anti-RPS8 antibody [EPR17334] ab201454)
Predicted band size: 24 kDa
This data was developed using Anti-RPS8 antibody [EPR17334] ab201454, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton-X100 permeabilized Jurkat (Human T cell leukemia cells from peripheral blood) cells labeling RPS8 with Anti-RPS8 antibody [EPR17334] ab201454 at 1/600 dilution, followed by AlexaFluor®488 Goat anti-Rabbit secondary antibody (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/500 dilution (green). Confocal image showing cytoplasmic staining on Jurkat cell line. The nuclear counter stain is DAPI (blue). Tubulin is stained with Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 anti-Tubulin (mouse mAb) at 1/1000 dilution, followed by AlexaFluor®594 Goat anti-Mouse secondary antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at 1/500 dilution (red).
-ve control 1: Anti-RPS8 antibody [EPR17334] ab201454 at 1/600 dilution followed by AlexaFluor®594 Goat anti-Mouse secondary antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at 1/500 dilution.
-ve control 2: Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 anti-Tubulin (mouse mAb) at 1/1000 dilution, followed by AlexaFluor®488 Goat anti-Rabbit secondary antibody (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/500 dilution.
This data was developed using Anti-RPS8 antibody [EPR17334] ab201454, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 2% paraformaldehyde-fixed A549 (Human lung carcinoma) cells labeling RPS8 with Anti-RPS8 antibody [EPR17334] ab201454 at 1/250 dilution (red) compared with a rabbit monoclonal IgG isotype control (black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (FITC) at 1/150 dilution was used as the secondary antibody.
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com