Cell Biology Antibodies 8

Anti-DRP1 Antibody (CAB2586)

(No reviews yet) Write a Review
SKU:
CAB2586
Product Type:
Antibody
Reactivity:
Human
Reactivity:
Mouse
Reactivity:
Rat
Host Species:
Rabbit
Isotype:
IgG
Research Area:
Cell Biology

Description

system_update_altDatasheetsystem_update_altMSDS
Antibody Name:Anti-DRP1 Antibody
Antibody SKU:CAB2586
Antibody Size:20uL, 50uL, 100uL
Application:WB IF
Reactivity:Human, Mouse, Rat
Host Species:Rabbit
Immunogen:Recombinant fusion protein containing a sequence corresponding to amino acids 411-710 of human DRP1 (NP_036193.2).
Application:WB IF
Recommended Dilution:WB 1:500 - 1:2000 IF 1:50 - 1:200
Reactivity:Human, Mouse, Rat
Positive Samples:Mouse brain, Rat brain
Immunogen:Recombinant fusion protein containing a sequence corresponding to amino acids 411-710 of human DRP1 (NP_036193.2).
Purification Method:Affinity purification
Storage Buffer:Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Isotype:IgG
Sequence:VSFE LLVK RQIK RLEE PSLR CVEL VHEE MQRI IQHC SNYS TQEL LRFP KLHD AIVE VVTC LLRK RLPV TNEM VHNL VAIE LAYI NTKH PDFA DACG LMNN NIEE QRRN RLAR ELPS AVSR DKLI QDSR RETK NVAS GGGG VGDG VQEP TTGN WRGM LKTS KAEE LLAE EKSK PIPI MPAS PQKG HAVN LLDV PVPV ARKL SARE QRDC EVIE RLIK SYFL IVRK NIQD SVPK AVMH FLVN HVKD TLQS ELVG QLYK SSLL DDLL TESE DMAQ RRKE AADM LKAL QGAS QIIA EIRE THLW
Gene ID:10059
Uniprot:O00429
Cellular Location:Cytoplasm, Cytoplasmic vesicle, Endomembrane system, Golgi apparatus, Membrane, Mitochondrion outer membrane, Peripheral membrane protein, Peroxisome, clathrin-coated pit, cytosol, secretory vesicle, synaptic vesicle membrane
Calculated MW:60kDa/78kDa/79kDa/80kDa/81kDa/82kDa/83kDa
Observed MW:78KDa
Synonyms:DNM1L, DLP1, DRP1, DVLP, DYMPLE, EMPF, EMPF1, HDYNIV
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.
UniProt Protein Function:DRP1: Functions in mitochondrial and peroxisomal division. Mediates membrane fission through oligomerization into ring-like structures which wrap around the scission site to constict and sever the mitochondrial membrane through a GTP hydrolysis- dependent mechanism. Required for normal brain development. Facilitates developmentally-regulated apoptosis during neural tube development. Required for a normal rate of cytochrome c release and caspase activation during apoptosis. Also required for mitochondrial fission during mitosis. May be involved in vesicle transport. Homotetramer; dimerizes through the N-terminal GTP-middle region of one molecule binding to the GED domain of another DNM1L molecule. Can self-assemble in multimeric ring-like structures. Interacts with BCL2L1; the interaction stimulates the GTPase activity of DMN1L in synapses and increases the number of axonal mitochondria and the size and number of synaptic vesicle clusters. Interacts with FIS1. Interacts with GSK3B and MARCH5. Interacts (via the GTPase and B domains) with UBE2I; the interaction promotes sumoylation of DNM1L, mainly in ite B domain. Interacts with PPP3CA; the interaction dephosphorylates DNM1L and regulates its transition to mitochondria. Interacts witn MID49 and MID51. 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 brain, heart and kidney. Isoform 5 is dominantly expressed in liver, heart and kidney. Isoform 6 is expressed in neurons. Belongs to the dynamin family. 6 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Endoplasmic reticulum; Mitochondrial; Microtubule-binding; EC 3.6.5.5; Apoptosis; Hydrolase; Motor

Chromosomal Location of Human Ortholog: 12p11.21

Cellular Component: Golgi apparatus; microtubule; protein complex; intracellular membrane-bound organelle; synaptic vesicle membrane; mitochondrion; coated pit; cytosol; mitochondrial outer membrane; membrane; perinuclear region of cytoplasm; cytoplasm; peroxisome; cell junction

Molecular Function:GTPase activity; identical protein binding; protein binding; protein homodimerization activity; GTP binding; ubiquitin protein ligase binding; lipid binding

Biological Process: peroxisome fission; mitochondrial fission; release of cytochrome c from mitochondria; positive regulation of protein secretion; positive regulation of apoptosis; apoptosis; metabolic process; regulation of protein oligomerization; endocytosis; mitochondrial fragmentation during apoptosis; cell structure disassembly during apoptosis; protein homotetramerization

Disease: Encephalopathy, Lethal, Due To Defective Mitochondrial And Peroxisomal Fission

NCBI Summary: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 Code:O00429
NCBI GenInfo Identifier:125987821
NCBI Gene ID:10059
NCBI Accession:O00429.2
UniProt Secondary Accession:O00429,O14541, O60709, Q59GN9, Q7L6B3, Q8TBT7, Q9BWM1 Q9Y5J2, A8K4X9, B4DGC9, B4DSU8, J3KPI2,
UniProt Related Accession:O00429
Molecular Weight:736
NCBI Full Name:Dynamin-1-like protein
NCBI Synonym Full Names:dynamin 1-like
NCBI Official Symbol:DNM1L  
NCBI Official Synonym Symbols:DLP1; DRP1; DVLP; EMPF; DYMPLE; HDYNIV  
NCBI Protein Information:dynamin-1-like protein; dynamin-like protein 4; dynamin-like protein IV; Dnm1p/Vps1p-like protein; dynamin-related protein 1; dynamin family member proline-rich carboxyl-terminal domain less
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
Protein Family:Dynamin-1-like protein
UniProt Gene Name:DNM1L  
UniProt Entry Name:DNM1L_HUMAN
Anti-DRP1 Antibody (CAB2586)Western blot analysis of extracts of various cell lines, using DRP1 Rabbit pAb (CAB2586) at 1:8000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 1s.
Anti-DRP1 Antibody (CAB2586)Immunofluorescence analysis of HeLa cells using DRP1 antibody (CAB2586). Blue: DAPI for nuclear staining.
View AllClose

0 Reviews

View AllClose

Related Products

DRP1 Monoclonal Antibody

DRP1 Monoclonal Antibody

OverviewProduct Name:DRP1 Monoclonal AntibodyProduct Code:CAB21968Reactivity:Human, Mouse, RatApplications:Western blotting, Immu
DRP1 Polyclonal Antibody

DRP1 Polyclonal Antibody

OverviewProduct Name:DRP1 Polyclonal AntibodyProduct Code:CAB21310Reactivity:Human, RatApplications:Western blotting, Immunofluor