MCU 产品
(Mitochondrial Calcium Uniporter (MCU))
Categories
This gene encodes a calcium transporter that localizes to the mitochondrial inner membrane. The encoded protein interacts with mitochondrial calcium uptake 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012].
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Featured MCU Categories
MCU 抗体
High quality antibodies with extensive validation data.
MCU ELISA试剂盒
Reliable ELISA kits for a wide range of species.
MCU 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended MCU 抗体
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Human
Application
WB, IF
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- (4)
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ABIN7268549
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, IHC, WB
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- (3)
Cat. No.
ABIN7146314
Quantity
100 μg
Datasheet
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Reactivity
Human, Mouse
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- (2)
Cat. No.
ABIN6260526
Quantity
100 μL
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Recommended MCU ELISA试剂盒
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Rat
Analytical Method
Quantitative Competition ELISA
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Cat. No.
ABIN1744117
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Human
Analytical Method
Quantitative Competition ELISA
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Cat. No.
ABIN1742896
Quantity
96 tests
Datasheet
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Reactivity
Sheep
Analytical Method
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ABIN1773800
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Recommended MCU 蛋白
Latest Publications for our MCU Products
: "Effects of luteolin on regulatory proteins and enzymes for myocyte calcium circulation in hypothermic preserved rat heart." in: Experimental and therapeutic medicine, Vol. 15, Issue 2, pp. 1433-1441, (2018) (PubMed).: "Structure and function of the N-terminal domain of the human mitochondrial calcium uniporter." in: EMBO reports, Vol. 16, Issue 10, pp. 1318-33, (2015) (PubMed).
: "Quantitative proteomics of synaptic and nonsynaptic mitochondria: insights for synaptic mitochondrial vulnerability." in: Journal of proteome research, Vol. 13, Issue 5, pp. 2620-36, (2014) (PubMed).
: "Reconstitution of the mitochondrial calcium uniporter in yeast." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Issue 24, pp. 8985-90, (2014) (PubMed).
: "Chronic enrichment of hepatic endoplasmic reticulum-mitochondria contact leads to mitochondrial dysfunction in obesity." in: Nature medicine, Vol. 20, Issue 12, pp. 1427-35, (2014) (PubMed).
: "Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. ..." in: Nature genetics, Vol. 46, Issue 2, pp. 188-93, (2014) (PubMed).
: "Mitochondrial calcium uniporter MCU supports cytoplasmic Ca2+ oscillations, store-operated Ca2+ entry and Ca2+-dependent gene expression in response to receptor stimulation." in: PLoS ONE, Vol. 9, Issue 7, pp. e101188, (2014) (PubMed).
: "Mitochondrial calcium uniporter Mcu controls excitotoxicity and is transcriptionally repressed by neuroprotective nuclear calcium signals." in: Nature communications, Vol. 4, pp. 2034, (2013) (PubMed).
: "The physiological role of mitochondrial calcium revealed by mice lacking the mitochondrial calcium uniporter." in: Nature cell biology, Vol. 15, Issue 12, pp. 1464-72, (2013) (PubMed).
: "Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter." in: Nature, Vol. 476, Issue 7360, pp. 341-5, (2011) (PubMed).
Synonyms and alternative names related to MCU
mitochondrial calcium uniporter (MCU), mitochondrial calcium uniporter (Mcu), 2010012O16Rik, AV064928, C10orf42, CCDC109A, Ccdc109a, D130073L02Rik, Gm64Protein level used designations for MCU
- calcium uniporter protein, mitochondrial
- coiled-coil domain-containing protein 109A
- coiled-coil domain containing 109A
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