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MTO1 Polyclonal antibody

MTO1 Polyclonal Antibody for IF, WB,ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, IF, CoIP, ELISA

Conjugate

Unconjugated

Cat no : 15650-1-AP

Synonyms

CGI 02, MTO1



Tested Applications

Positive WB detected inMCF-7 cells, human liver tissue
Positive IF detected inMCF-7 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:2000
Immunofluorescence (IF)IF : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

15650-1-AP targets MTO1 in WB, IF, CoIP, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Cited Reactivityhuman
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen MTO1 fusion protein Ag8192
Full Name mitochondrial translation optimization 1 homolog (S. cerevisiae)
Calculated Molecular Weight 717 aa, 80 kDa
Observed Molecular Weight 70-75 kDa
GenBank Accession NumberBC005808
Gene Symbol MTO1
Gene ID (NCBI) 25821
RRIDAB_2266805
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Protocols

Product Specific Protocols
WB protocol for MTO1 antibody 15650-1-APDownload protocol
IF protocol for MTO1 antibody 15650-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

Nucleic Acids Res

Restoration of mitochondrial function through activation of hypomodified tRNAs with pathogenic mutations associated with mitochondrial diseases

Authors - Ena Tomoda
humanWB

Nat Commun

RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis.

Authors - Uwe Richter
humanCoIP

Nucleic Acids Res

The human tRNA taurine modification enzyme GTPBP3 is an active GTPase linked to mitochondrial diseases.

Authors - Gui-Xin Peng
humanWB

J Hepatol

Severe respiratory complex III defect prevents liver adaptation to prolonged fasting.

Authors - Laura S Kremer
humanWB

Am J Hum Genet

Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosis.

Authors - Ghezzi Daniele D
humanWB

Hum Mol Genet

Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency.

Authors - Boczonadi Veronika V