Key features and details
- Rabbit polyclonal to RPS3A
- Suitable for: WB, ICC/IF
- Reacts with: Human
- Isotype: IgG
Product nameAnti-RPS3A antibody
See all RPS3A primary antibodies
DescriptionRabbit polyclonal to RPS3A
Tested applicationsSuitable for: WB, ICC/IFmore details
Species reactivityReacts with: Human
Predicted to work with: Mouse, Rat, Pig, Zebrafish
Recombinant fragment corresponding to a region within amino acids 14-262 of Human RPS3A (NP_000997).
- 293T, A431, H1299, HeLaS3, HepG2, Molt-4 and Raji whole cell lysates; HeLa cells.
Storage instructionsShipped at 4°C. Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Storage bufferpH: 7.00
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 1.21% Tris, 0.75% Glycine, 20% Glycerol
Concentration information loading...
PurityImmunogen affinity purified
Our Abpromise guarantee covers the use of ab96534 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/500 - 1/3000. Predicted molecular weight: 30 kDa.|
|ICC/IF||1/100 - 1/200.|
FunctionMay play a role during erythropoiesis through regulation of transcription factor DDIT3.
Sequence similaritiesBelongs to the ribosomal protein S3Ae family.
Cellular localizationCytoplasm. Nucleus. Localized in cytoplasmic mRNP granules containing untranslated mRNAs.
- Information by UniProt
- 40S ribosomal protein S3a antibody
- Fte 1 antibody
- Fte-1 antibody
All lanes : Anti-RPS3A antibody (ab96534) at 1/1000 dilution
Lane 1 : 293T whole cell lysate
Lane 2 : A431 whole cell lysate
Lane 3 : H1299 whole cell lysate
Lane 4 : HeLa S3 whole cell lysate
Lane 5 : Hep G2 whole cell lysate
Lane 6 : Molt4 whole cell lysate
Lane 7 : Raji whole cell lysate
Lysates/proteins at 30 µg per lane.
Predicted band size: 30 kDa
ab96534, at 1/200 dilution, staining paraformaldehyde-fixed HeLa cells by Immunofluorescence. Lower image is merged with DNA probe.
ab96534 has not yet been referenced specifically in any publications.