Full Product Name
Phospho-DRP1 (Ser637) Antibody
Product Gene Name
anti-DRP1 antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for O00429
Other Notes
Small volumes of anti-DRP1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Western Blot (WB) of anti-DRP1 antibody
Western blot analysis Phospho-DRP1 (Ser637) using 293 whole cell lysates

NCBI/Uniprot data below describe general gene information for DRP1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001265392.1
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NCBI GenBank Nucleotide #
NM_001278463.1
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UniProt Primary Accession #
O00429
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UniProt Secondary Accession #
O14541; O60709; Q59GN9; Q7L6B3; Q8TBT7; Q9BWM1; Q9Y5J2; A8K4X9; B4DGC9; B4DSU8; J3KPI2[Other Products]
UniProt Related Accession #
O00429[Other Products]
Molecular Weight
82,057 Da
NCBI Official Full Name
dynamin-1-like protein isoform 4
NCBI Official Synonym Full Names
dynamin 1 like
NCBI Official Symbol
DNM1L [Similar Products]
NCBI Official Synonym Symbols
DLP1; DRP1; DVLP; EMPF; OPA5; EMPF1; DYMPLE; HDYNIV
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NCBI Protein Information
dynamin-1-like protein
UniProt Protein Name
Dynamin-1-like protein
UniProt Synonym Protein Names
Dnm1p/Vps1p-like protein; DVLP; Dynamin family member proline-rich carboxyl-terminal domain less; Dymple; Dynamin-like protein; Dynamin-like protein 4; Dynamin-like protein IV; HdynIV; Dynamin-related protein 1
UniProt Gene Name
DNM1L [Similar Products]
UniProt Synonym Gene Names
DLP1; DRP1; DVLP; Dymple; HdynIV [Similar Products]
NCBI Summary for DRP1
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. [provided by RefSeq, Jun 2013]
UniProt Comments for DRP1
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. Plays an important role in mitochondrial fission during mitosis (PubMed:26992161). 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.
Research Articles on DRP1
1. Results uncovered a novel mechanism of Drp1-mediated mitochondrial fragmentation in senecionine-induced liver injury.
Precautions
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