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MTO1 Polyclonal antibody

MTO1 Polyclonal Antibody for WB, IF/ICC, ELISA
Cat No. 15650-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

WB, IF/ICC, ELISA and More (1)

Protein MTO1 homolog, mitochondrial, CGI-02, CGI 02

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -


经过测试的应用

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

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:500-1:2000
Immunofluorescence (IF)/ICCIF/ICC : 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.

产品信息

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

经测试应用 WB, IF/ICC, ELISA Application Description
文献引用应用WB, CoIP
经测试反应性 human
文献引用反应性human
免疫原 MTO1 fusion protein Ag8192 种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 mitochondrial translation optimization 1 homolog (S. cerevisiae)
别名 Protein MTO1 homolog, mitochondrial, CGI-02, CGI 02
计算分子量 717 aa, 80 kDa
观测分子量 70-75 kDa
GenBank蛋白编号BC005808
基因名称 MTO1
Gene ID (NCBI) 25821
RRIDAB_2266805
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ9Y2Z2
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

实验方案

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

发表文章

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
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