Key features and details
- Rabbit polyclonal to MTO1
- Suitable for: WB, IHC-P
- Reacts with: Rat, Human
- Isotype: IgG
Product nameAnti-MTO1 antibody
DescriptionRabbit polyclonal to MTO1
Tested applicationsSuitable for: WB, IHC-Pmore details
Species reactivityReacts with: Rat, Human
Recombinant fragment corresponding to Human MTO1 aa 420-680.
Database link: Q9Y2Z2
- WB: Rat heart tissue lysate; Jurkat whole cell lysate. IHC-P: Human kidney tissue.
Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
Storage bufferpH: 7.30
Preservative: 0.02% Sodium azide
Constituents: PBS, 50% Glycerol (glycerin, glycerine)
Concentration information loading...
PurityProtein G purified
Purification notesPurity >95%
Our Abpromise guarantee covers the use of ab235381 in the following tested applications.
|WB||1/1000 - 1/5000.|
|IHC-P||1/20 - 1/200.|
RelevanceThe Protein MTO1 homolog is involved in the 5 carboxymethylaminomethyl modification (mnm(5)s(2)U34) of the wobble uridine base in mitochondrial tRNAs. It is ubiquitously expressed in various tissues, but with a markedly elevated expression in tissues of high metabolic rates including cochlea. The protein belongs to the gidA family.
- mitochondrial MTO1 3 antibody
- mitochondrial translation optimization 1 homolog antibody
- protein MTO1 homolog, mitochondrial precursor antibody
Paraffin-embedded human kidney tissue stained for MTO1 using ab235381 at 1/100 dilution in immunohistochemical analysis.
All lanes : Anti-MTO1 antibody (ab235381) at 1/500 dilution
Lane 1 : Rat heart tissue lysate
Lane 2 : Jurkat (human T cell leukemia cell line from peripheral blood) whole cell
All lanes : Goat polyclonal to rabbit IgG at 1/10000 dilution
Observed band size: 80,35 kDa why is the actual band size different from the predicted?
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
ab235381 has not yet been referenced specifically in any publications.