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Registration enables users to use special features of this website, such as past
order histories, retained contact details for faster checkout, review submissions, and special promotions.
Registration enables users to use special features of this website, such as past
order histories, retained contact details for faster checkout, review submissions, and special promotions.
Registration enables users to use special features of this website, such as past
order histories, retained contact details for faster checkout, review submissions, and special promotions.
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DNM1L / DRP1
dynamin 1-like
Functions in mitochondrial and peroxisomal division. Mediates membrane fission through oligomerization into membrane-associated tubular structures that wrap around the scission site to constrict and sever the mitochondrial membrane through a GTP hydrolysis-dependent mechanism. Through its function in mitochondrial division, ensures the survival of at least some types of postmitotic neurons, including Purkinje cells, by suppressing oxidative damage. Required for normal brain development, including that of cerebellum. Facilitates developmentally regulated apoptosis during neural tube formation. Required for a normal rate of cytochrome c release and caspase activation during apoptosis; this requirement may depend upon the cell type and the physiological apoptotic cues. Also required for mitochondrial fission during mitosis. Required for formation of endocytic vesicles. Proposed to regulate synaptic vesicle membrane dynamics through association with BCL2L1 isoform Bcl-X(L) which stimulates its GTPase activity in synaptic vesicles; the function may require its recruitment by MFF to clathrin-containing vesicles. Required for programmed necrosis execution.Isoform 1 and isoform 4 inhibit peroxisomal division when overexpressed.
Gene Name:
dynamin 1-like
Synonyms:
DNM1L, DYMPLE, Dynamin 1-like, Dynamin-like protein, Dynamin-like protein 4, Dynamin-like protein IV, DLP1, Dnm1p/Vps1p-like protein, DVLP, Dynamin-related protein 1, DYNIV-11, DRP1, Dynamin-1-like protein, VPS1, EMPF, HDYNIV
Sensory neuropathy attributable to loss of Bcl-w. Courchesne SL, Karch C, Pazyra-Murphy MF, Segal RA. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2011 31:1624-34. (WB; Mouse)
[PubMed:21289171]
[PMC:PMC3074348]
2
Impaired mitochondrial dynamics and abnormal interaction of amyloid beta with mitochondrial protein Drp1 in neurons from patients with Alzheimer's disease: implications for neuronal damage. Manczak M, Calkins MJ, Reddy PH. Human molecular genetics. 2011 20:2495-509.
[PubMed:21459773]
[PMC:PMC3109997]
3
High-mobility group box 1 is essential for mitochondrial quality control. Tang D, Kang R, Livesey KM, Kroemer G, Billiar TR, Van Houten B, Zeh HJ, Lotze MT. Cell metabolism. 2011 13:701-11. (ICC, WB; Mouse)
[PubMed:21641551]
[PMC:PMC3293110]
4
Role of Drp1, a key mitochondrial fission protein, in neuropathic pain. Ferrari LF, Chum A, Bogen O, Reichling DB, Levine JD. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2011 31:11404-10.
[PubMed:21813700]
[PMC:PMC3157245]
5
Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease. Calkins MJ, Manczak M, Mao P, Shirendeb U, Reddy PH. Human molecular genetics. 2011 20:4515-29.
[PubMed:21873260]
[PMC:PMC3209824]
6
Inhibition of mitochondrial fission prevents cell cycle progression in lung cancer. Rehman J, Zhang HJ, Toth PT, Zhang Y, Marsboom G, Hong Z, Salgia R, Husain AN, Wietholt C, Archer SL. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2012 26:2175-86. (IHC, WB; Human)
[PubMed:22321727]
[PMC:PMC3336787]
7
Dynamin-related protein 1 heterozygote knockout mice do not have synaptic and mitochondrial deficiencies. Manczak M, Sesaki H, Kageyama Y, Reddy PH. Biochimica et biophysica acta. 2012 1822:862-74. (WB; Mouse)
[PubMed:22387883]
[PMC:PMC3338881]
8
Dynamin-related protein 1-mediated mitochondrial mitotic fission permits hyperproliferation of vascular smooth muscle cells and offers a novel therapeutic target in pulmonary hypertension. Marsboom G, Toth PT, Ryan JJ, Hong Z, Wu X, Fang YH, Thenappan T, Piao L, Zhang HJ, Pogoriler J, Chen Y, Morrow E, Weir EK, Rehman J, Archer SL. Circulation research. 2012 110:1484-97. (ICC, IHC, WB; Human)
[PubMed:22511751]
[PMC:PMC3539779]
9
High fat diet induced developmental defects in the mouse: oocyte meiotic aneuploidy and fetal growth retardation/brain defects. Luzzo KM, Wang Q, Purcell SH, Chi M, Jimenez PT, Grindler N, Schedl T, Moley KH. PloS one. 2012 7:e49217. (ICC, IHC; Mouse)
[PubMed:23152876]
[PMC:PMC3495769]
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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.
The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).