CYTB | Proteintech Group 55090-1-AP product information

This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.

product summary

company name :

Proteintech Group

product type :

antibody

product name :

CYTB

catalog :

55090-1-AP

quantity :

150UL

price :

299 USD

clonality :

polyclonal

host :

domestic rabbit

conjugate :

nonconjugated

reactivity :

human

application :

western blot, ELISA, immunohistochemistry

citations: 26

Published Application/Species/Sample/Dilution	Reference
western blot; human; 1:1000; loading ...; fig s2e, s2g	Richter U, Ng K, Suomi F, Marttinen P, Turunen T, Jackson C, et al. Mitochondrial stress response triggered by defects in protein synthesis quality control. Life Sci Alliance. 2019;2: pubmed publisher
western blot; human; fig 6a	Meng F, Cang X, Peng Y, Li R, Zhang Z, Li F, et al. Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation. J Biol Chem. 2017;292:2881-2892 pubmed publisher
western blot; human; fig 5	Jiang P, Wang M, Xue L, Xiao Y, Yu J, Wang H, et al. A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function. Mol Cell Biol. 2016;36:1920-30 pubmed publisher
	Ma Y, Zhu S, Lv T, Gu X, Feng H, Zhen J, et al. SQSTM1/p62 Controls mtDNA Expression and Participates in Mitochondrial Energetic Adaption via MRPL12. iScience. 2020;23:101428 pubmed publisher
	Zhang S, Reljic B, Liang C, Kerouanton B, Francisco J, Peh J, et al. Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assembly. Nat Commun. 2020;11:1312 pubmed publisher
	Li K, Wu L, Liu J, Lin W, Qi Q, Zhao T. Maternally Inherited Diabetes Mellitus Associated with a Novel m.15897G>A Mutation in Mitochondrial tRNAThr Gene. J Diabetes Res. 2020;2020:2057187 pubmed publisher
	Gong S, Wang X, Meng F, Cui L, Yi Q, Zhao Q, et al. Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHis mutation. J Biol Chem. 2020;295:940-954 pubmed publisher
	Zhuang X, Chen Y, Wu Z, Xu Q, Chen M, Shao M, et al. Mitochondrial miR-181a-5p promotes glucose metabolism reprogramming in liver cancer by regulating the electron transport chain. Carcinogenesis. 2019;: pubmed publisher
	Zhao X, Cui L, Xiao Y, Mao Q, Aishanjiang M, Kong W, et al. Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript. Nucleic Acids Res. 2019;47:10340-10356 pubmed publisher
	Fu R, Yang P, Li Z, Liu W, Amin S, Li Z. Avenanthramide A triggers potent ROS-mediated anti-tumor effects in colorectal cancer by directly targeting DDX3. Cell Death Dis. 2019;10:593 pubmed publisher
	Iershov A, Nemazanyy I, Alkhoury C, Girard M, Barth E, Cagnard N, et al. The class 3 PI3K coordinates autophagy and mitochondrial lipid catabolism by controlling nuclear receptor PPARα. Nat Commun. 2019;10:1566 pubmed publisher
	Jia Z, Zhang Y, Li Q, Ye Z, Liu Y, Fu C, et al. A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis. Nucleic Acids Res. 2019;47:2056-2074 pubmed publisher
	Wang L, Yan Z, Vihinen H, Eriksson O, Wang W, Soliymani R, et al. FAM92A1 is a BAR domain protein required for mitochondrial ultrastructure and function. J Cell Biol. 2019;218:97-111 pubmed publisher
	Aulas A, Lyons S, Fay M, Anderson P, Ivanov P. Nitric oxide triggers the assembly of "type II" stress granules linked to decreased cell viability. Cell Death Dis. 2018;9:1129 pubmed publisher
	Richter U, Evans M, Clark W, Marttinen P, Shoubridge E, Suomalainen A, et al. RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis. Nat Commun. 2018;9:3966 pubmed publisher
	Zhang J, Ji Y, Lu Y, Fu R, Xu M, Liu X, et al. Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagy. Hum Mol Genet. 2018;27:1999-2011 pubmed publisher
	Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y, et al. Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation. J Biol Chem. 2018;293:3321-3334 pubmed publisher
	Zhang J, Ji Y, Liu X, Chen J, Wang B, Zhang M, et al. Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNAThr in eight Chinese pedigrees. Mitochondrion. 2018;42:84-91 pubmed publisher
	Zhou M, Xue L, Chen Y, Li H, He Q, Wang B, et al. A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function. J Biol Chem. 2018;293:1425-1438 pubmed publisher
	Glasgow R, Thompson K, Barbosa I, He L, Alston C, Deshpande C, et al. Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits. Neurogenetics. 2017;18:227-235 pubmed publisher
	Zhou M, Wang M, Xue L, Lin Z, He Q, Shi W, et al. A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR). J Biol Chem. 2017;292:13934-13946 pubmed publisher
	You Y, Zhang Y, Lu Y, Hu K, Qu X, Liu Y, et al. Protein profiling and functional analysis of liver mitochondria from rats with nonalcoholic steatohepatitis. Mol Med Rep. 2017;16:2379-2388 pubmed publisher
	Chen X, Nie Z, Wang F, Wang J, Liu X, Zheng J, et al. Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNAPhe gene. Mitochondrion. 2017;35:111-118 pubmed publisher
	Wang M, Peng Y, Zheng J, Zheng B, Jin X, Liu H, et al. A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function. Nucleic Acids Res. 2016;44:10974-10985 pubmed
	Wang M, Liu H, Zheng J, Chen B, Zhou M, Fan W, et al. A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction. J Biol Chem. 2016;291:21029-21041 pubmed
	Jiang P, Jin X, Peng Y, Wang M, Liu H, Liu X, et al. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. Hum Mol Genet. 2016;25:584-96 pubmed publisher

product information

CatalogNo :

55090-1-AP

AntigenName :

CYTB

Package :

150UL

Price :

299 USD

Exsists20ul :

20ul trial size available

FullName :

cytochrome b

Immunogen :

Peptide

Species :

human, mouse, rat

Host :

Rabbit

IsConjugated :

Unconjugated

AntigenSpecies :

human

Application :

WB, IHC, ELISA

Clonlity :

Polyclonal

IsoType :

IgG

Synonyms :

COB, Complex III subunit 3, Complex III subunit III, CYTB, cytochrome b, MT CYB, MTCYB

PrimaryOrSecondary :

Primary

AntibodyBuffer :

0.1M NaHCO3, 0.1M glycine, 0.02% sodium azide and 50% glycerol pH 7.3.

GenBankNo :

YP_003024038

Category :

Binding Proteins;Cytoskeleton/Scaffold Proteins;Membrane Proteins;Metabolism;Transport/Trafficking;

PurifyMethod :

Antigen affinity purification

NewAb :

False

IsSellable :

True

AppTiter :

IHC 1:200 ; WB 1:600 ;