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Recombinant Human Dynamin-1-like protein (DNM1L)

The expression region of this recombinant Human DNM1L covers amino acids 1-710. The expected molecular weight for the DNM1L protein is calculated to be 84.4 kDa. This protein is generated in a e.coli-based system. The DNM1L gene fragment has been modified by fusing the N-terminal 10xHis tag and C-terminal Myc tag, providing convenience in detecting and purifying the recombinant DNM1L protein during the following stages.Human dynamin-1-like protein (DNM1L) is a critical regulator of mitochondrial dynamics. It plays a central role in mitochondrial fission, a process essential for maintaining mitochondrial morphology, distribution, and function. DNM1L facilitates the division of mitochondria into smaller units, allowing for their proper distribution during cell division and ensuring mitochondrial quality control. Dysregulation of mitochondrial dynamics, often associated with abnormal DNM1L activity, is implicated in various diseases, including neurodegenerative disorders and cancer. Understanding the intricate role of DNM1L in mitochondrial dynamics is crucial for unraveling its implications in health and disease and exploring potential therapeutic interventions targeting mitochondrial function.

ACP02416

The expression region of this recombinant Human DNM1L covers amino acids 1-710. The expected molecular weight for the DNM1L protein is calculated to be 84.4 kDa. This protein is generated in a e.coli-based system. The DNM1L gene fragment has been modified by fusing the N-terminal 10xHis tag and C-terminal Myc tag, providing convenience in detecting and purifying the recombinant DNM1L protein during the following stages.Human dynamin-1-like protein (DNM1L) is a critical regulator of mitochondrial dynamics. It plays a central role in mitochondrial fission, a process essential for maintaining mitochondrial morphology, distribution, and function. DNM1L facilitates the division of mitochondria into smaller units, allowing for their proper distribution during cell division and ensuring mitochondrial quality control. Dysregulation of mitochondrial dynamics, often associated with abnormal DNM1L activity, is implicated in various diseases, including neurodegenerative disorders and cancer. Understanding the intricate role of DNM1L in mitochondrial dynamics is crucial for unraveling its implications in health and disease and exploring potential therapeutic interventions targeting mitochondrial function.

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Specifications


Cat.No ACP02416 Target NameDNM1L
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range1-710aaMol Weight84.4 kDa
Protein LengthFull Length of Isoform 2PurityGreater than 85% as determined by SDS-PAGE.
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDO00429
Background Information
  • Uniprot Id

    O00429

  • Target Species

    Human

  • Target Name

    DNM1L

  • Target Full Name

    Dynamin-1-like protein

  • Target Function

    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. The specific recruitment at scission sites is mediated by membrane receptors like MFF, MIEF1 and MIEF2 for mitochondrial membranes. While the recruitment by the membrane receptors is GTP-dependent, the following hydrolysis of GTP induces the dissociation from the receptors and allows DNM1L filaments to curl into closed rings that are probably sufficient to sever a double membrane. Acts downstream of PINK1 to promote mitochondrial fission in a PRKN-dependent manner. Plays an important role in mitochondrial fission during mitosis. 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. 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. Rhythmic control of its activity following phosphorylation at Ser-637 is essential for the circadian control of mitochondrial ATP production.; Inhibits peroxisomal division when overexpressed.; Inhibits peroxisomal division when overexpressed.

  • Target Involvement

    Encephalopathy due to defective mitochondrial and peroxisomal fission 1 (EMPF1)

  • Target Subcellular Location

    Cytoplasm, cytosol. Golgi apparatus. Endomembrane system; Peripheral membrane protein. Mitochondrion outer membrane; Peripheral membrane protein. Peroxisome. Membrane, clathrin-coated pit. Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane.

  • Target Protein Families

    TRAFAC class dynamin-like GTPase superfamily, Dynamin/Fzo/YdjA family

  • Target Tissue Specificity

    Ubiquitously expressed with highest levels found in skeletal muscles, heart, kidney and brain. Isoform 1 is brain-specific. Isoform 2 and isoform 3 are predominantly expressed in testis and skeletal muscles respectively. Isoform 4 is weakly expressed in b

  • Target Research Area

    Cancer

  • Target Synonyms

    DLP1; dnm1l; DNM1L_HUMAN; Dnm1p/Vps1p-like protein; dnml1; DRP1; DVLP; Dymple; Dynamin 1 like; Dynamin family member proline-rich carboxyl-terminal domain less; Dynamin like protein; Dynamin related protein 1; Dynamin-1-like protein; Dynamin-like protein 4; Dynamin-like protein; Dynamin-like protein IV; Dynamin-related protein 1; DYNIV 11; EMPF; EMPF1; FLJ41912; HdynIV; VPS1

  • Target Background

    This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.

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