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The protein encoded by MFN1 is a mediator of mitochondrial fusion. 再加上，我们可以发Mitofusin 1 蛋白 (11) 和 Mitofusin 1 试剂盒 (5)和数多这个蛋白质的别的产品。
Showing 10 out of 138 products:
Human Monoclonal MFN1 Primary Antibody for RNAi, ELISA - ABIN527615
Zanna, Ghelli, Porcelli, Karbowski, Youle, Schimpf, Wissinger, Pinti, Cossarizza, Vidoni, Valentino, Rugolo, Carelli: OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. in Brain : a journal of neurology 2008
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Mouse (Murine) Monoclonal MFN1 Primary Antibody for ICC, IF - ABIN4334757
White, Puppa, Sato, Gao, Price, Baynes, Kostek, Matesic, Carson: IL-6 regulation on skeletal muscle mitochondrial remodeling during cancer cachexia in the ApcMin/+ mouse. in Skeletal muscle 2012
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Mammalian Monoclonal MFN1 Primary Antibody for ISt, IHC - ABIN1304823
Elezaby, Sverdlov, Tu, Soni, Luptak, Qin, Liesa, Shirihai, Rimer, Schaffer, Wilson S, Edward J: Mitochondrial remodeling in mice with cardiomyocyte-specific lipid overload. in Journal of molecular and cellular cardiology 2015
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Human Polyclonal MFN1 Primary Antibody for ICC, IF - ABIN4334755
Miller, Knaub, Olivera-Fragoso, Keller, Balasubramaniam, Watson, Reusch: Nitric oxide regulates vascular adaptive mitochondrial dynamics. in American journal of physiology. Heart and circulatory physiology 2013
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Human Polyclonal MFN1 Primary Antibody for FACS, IF (p) - ABIN670071
Lou, Guan, Liu, Liu, Zhang, Pan, Pei: The influence of chronic fluorosis on mitochondrial dynamics morphology and distribution in cortical neurons of the rat brain. in Archives of toxicology 2013
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Cow (Bovine) Polyclonal MFN1 Primary Antibody for WB - ABIN2787347
Bonala, McFarlane, Ang, Lim, Lee, Chua, Lokireddy, Sreekanth, Leow, Meng, Shyong, Lee, Gluckman, Sharma, Kambadur: Pid1 induces insulin resistance in both human and mouse skeletal muscle during obesity. in Molecular endocrinology (Baltimore, Md.) 2013
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The results showed that high level of Mfn1 expression significantly improved the embryo development rates by increasing ATP level and Deltapsim, while reducing H(2)O(2) generation.
Regulation of Mfn1 by MGRN1 (显示 MGRN1 抗体) and the proteasome modulates mitochondrial fusion.
SLC25A46 (显示 SLC25A46 抗体) is a new component in mitochondrial dynamics that serves as a regulator for MFN1/2 oligomerization.
MFN1-positive expression could be seen mainly in ganglion cells after 1 week of minus lens intervention, and with time extension, more and more positive cells appeared in the rod-cone cell and bipolar cell layer, and this phenomenon could not be found in the normal control eyes.
crystal structures of engineered human MFN1 containing the GTPase (显示 RACGAP1 抗体) domain and a helical domain during different stages of GTP (显示 AK3 抗体) hydrolysis; mechanistic model for MFN1-mediated mitochondrial tethering is proposed; results shed light on the molecular basis of mitochondrial fusion and mitofusin (显示 MFN2 抗体)-related human neuromuscular disorders
These results suggest that MFN (显示 TLL1 抗体) tethers apposing membranes, likely through nucleotide-dependent dimerization.
Improper transcriptional (in)activation of mitofusin-1 and dynamin-related protein 1 (显示 DNM1L 抗体) during early in vitro embryo development is associated with a decrease in mitochondrial membrane potential and with embryo fragmentation.
A fine balance of Mfn1 levels is maintained by MARCH5 (显示 MARCH5 抗体)-mediated quality control on acetylated Mfn1.
miR (显示 MLXIP 抗体)-19b targets 3'UTR (显示 UTS2R 抗体) sequences of Mfn1 genes inhibit the expression of Mfn1
In a amyotrophic lateral sclerosis transgenic mouse model, Mfn1 is significantly increased in spinal cord.
A novel role for the endoplasmic reticulum-associated Gp78 (显示 AMFR 抗体) ubiquitin ligase and the Mfn1 mitochondrial fusion factor in mitophagy.
These results highlight the crucial role of MFN1 in maintaining the competency of the STING pathway.
Despite apparent mitochondrial dysfunction, hearts deficient in both Mfn1 and Mfn2 (显示 MFN2 抗体) are protected against acute myocardial infarction due to impaired mitochondria/sarcoplasmic reticulum tethering.
We found that mouse embryonic fibroblasts lacking Mfn2 (显示 MFN2 抗体) have altered lipid droplet morphology. However, triacylglycerol biosynthesis was not dependent on ER-mitochondrial tethering mediated by mitofusins. Lastly, Mfn2 (显示 MFN2 抗体) does not have a role in adipocyte differentiation.
MFN1 deficiency leads to defects in mitochondrial activity and male infertility.
Report exposes a novel role for Shh (显示 SHH 抗体) in regulating mitochondrial dynamics and rescue the metabolic profile of tumor cells through regulation of mitofusin 1 and 2.
Ablating Mfn1 eliminates the cardiac-related lethality of Mff (显示 MFF 抗体) knockout mice.
Data suggest that mitochondrial fusion and fission events are regulated by four GTPases: Mfn1, Mfn2 (显示 MFN2 抗体), OPA1 (optic atrophy 1 (显示 OPA1 抗体) protein), and Drp1 (dynamin 1-like protein (显示 DNM1L 抗体)). [REVIEW]
Authors present evidence that metabolically challenged mitochondria undergo active fusion to suppress oxidative stress. In response to glucose starvation, mitofusin 1 (MFN1) becomes associated with the protein deacetylase HDAC6 (显示 HDAC6 抗体).
These findings suggest that mitochondrial impairment is a very early event in Alzheimer disease pathogenesis and abnormal expression of Mfn1 and Mfn2 (显示 MFN2 抗体) caused by excessive intracellular Abeta (显示 APP 抗体) is the possible molecular mechanism.
Data identify MFN1 as an ERK (显示 EPHB2 抗体) target to modulate mitochondrial shape and apoptosis.
The protein encoded by this gene is a mediator of mitochondrial fusion. This protein and mitofusin 2 are homologs of the Drosophila protein fuzzy onion (Fzo). They are mitochondrial membrane proteins that interact with each other to facilitate mitochondrial targeting.
, mitofusin 2
, fzo homolog
, mitochondrial transmembrane GTPase FZO-2
, mitochondrial transmembrane GTPase Fzo-1
, putative transmembrane GTPase
, transmembrane GTPase MFN1
, mitochondrial transmembrane GTPase FZO1B