Anti-DRP1 (phospho S616) antibody [EPR27387-57] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal DRP1 phospho S616 antibody. Carrier free. Suitable for WB, Dot and reacts with Human, Mouse, Rat, Transfected cell lysate - Human, Synthetic peptide samples. Cited in 1 publication.
View Alternative Names
DLP1, DRP1, DNM1L, Dynamin-1-like protein, Dnm1p/Vps1p-like protein, Dynamin family member proline-rich carboxyl-terminal domain less, Dynamin-like protein, Dynamin-like protein 4, Dynamin-like protein IV, Dynamin-related protein 1, DVLP, Dymple, HdynIV
- WB
Supplier Data
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] - BSA and Azide free (AB314756)
This data was developed using ab314755, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The identity of the lower MW band at approximately 20 kDa is unknown.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 19436752).
ab184247 was used as the loading control at a 1/1000 dilution.
All lanes:
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] (<a href='/en-us/products/primary-antibodies/drp1-phospho-s616-antibody-epr27387-57-ab314755'>ab314755</a>) at 1/1000 dilution
Lane 1:
Untreated HAP1 (human chronic myelogenous leukemia near-haploid cell line) whole cell lysate (untreated membrane) at 20 µg
Lane 2:
HAP1 treated with 100 ng/ml nocodazole for 16 hours whole cell lysate (untreated membrane) at 20 µg
Lane 3:
Untreated HAP1 (human chronic myelogenous leukemia near-haploid cell line) whole cell lysate (phosphatase treated membrane) at 20 µg
Lane 4:
HAP1 treated with 100 ng/ml nocodazole for 16 hours whole cell lysate (phosphatase treated membrane) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 82 kDa
Observed band size: 83 kDa
false
Exposure time: 92s
- WB
Supplier Data
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] - BSA and Azide free (AB314756)
This data was developed using ab314755, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. In western blot, anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution. In western blot, anti-DRP1 antibody [EPR19274] - Total protein Control (ab184247) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] (<a href='/en-us/products/primary-antibodies/drp1-phospho-s616-antibody-epr27387-57-ab314755'>ab314755</a>) at 1/1000 dilution
Lane 1:
PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate (untreated membrane) at 20 µg
Lane 2:
PC-12 whole cell lysate (phosphatase treated membrane) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 83 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] - BSA and Azide free (AB314756)
This data was developed using ab314755, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. The identity of the lower MW band at approximately 20 kDa (in lane 2) is unknown. In western blot, anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution. In western blot, anti-DRP1 antibody [EPR19274] - Total protein Control (ab184247) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] (<a href='/en-us/products/primary-antibodies/drp1-phospho-s616-antibody-epr27387-57-ab314755'>ab314755</a>) at 1/1000 dilution
Lane 1:
Untreated NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 2:
NIH/3T3 treated with /ml nocodazole for 17 hours whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 83 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] - BSA and Azide free (AB314756)
This data was developed using ab314755, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Immunoprecipitation experiments were performed with an anti-6X His tag® antibody (ab213204) at 1 : 5000 dilution. In western blot, anti-DRP1 antibody [EPR19274] - Total protein Control (ab184247) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] (<a href='/en-us/products/primary-antibodies/drp1-phospho-s616-antibody-epr27387-57-ab314755'>ab314755</a>) at 1/1000 dilution
Lane 1:
Untreated 293T cells transfected with a human DRP1 expression vector containi a myc-His-tag® lysate at 20 µg
Lane 2:
293T cells transfected with a human DRP1 expression vector containing a myc-His-tag®. Overexpressi cells were treated with 100/ml nocodazole for 17 hours whole cell lysate at 20 µg
Lane 3:
Untreated 293T cells transfected with a human DRP1(S616A mutant ) expression vector containi a myc-His-tag® lysate at 20 µg
Lane 4:
293T cells transfected with a human DRP1(S616A mutant) expression vector containing a myc-His-tag®. Overexpressi cells were treated with 100/ml nocodazole for 17 hours whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 83 kDa
false
Exposure time: 3s
- Dot
Supplier Data
Dot Blot - Anti-DRP1 (phospho S616) antibody [EPR27387-57] - BSA and Azide free (AB314756)
This data was developed using ab314755, the same antibody clone in a different buffer formulation. Dot blot analysis of DRP1 (phospho S616) using ab314755 at 1 : 1000 (0.514 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution. Exposure time : 180 seconds. Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Related conjugates and formulations (1)
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Anti-DRP1 (phospho S616) antibody [EPR27387-57]
Reactivity data
Product details
ab314756 is the carrier-free version of ab314755.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
DRP1 regulates mitochondrial morphology by controlling mitochondrial division. This process is essential in maintaining the balance between mitochondrial fission and fusion which affects mitochondrial distribution and function. DRP1 also associates with protein complexes involved in this dynamic balance including MFF (mitochondrial fission factor) and FIS1 (fission 1 protein). Phosphorylation state of DRP1 influences its activity; different phosphorylation sites either activate or inhibit its function.
Pathways
The mechanical action of DRP1 integrates closely into the mitochondrial quality control and apoptosis pathways. Mitochondrial fission driven by DRP1 is necessary for the removal of damaged mitochondria through mitophagy. It also influences the apoptotic pathway where DRP1 translocates to mitochondria under pro-apoptotic signals often in interaction with proteins such as Bax and Bak that promote cytochrome c release. This relationship affects cell survival and energy homeostasis.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Clinical and translational medicine 15:e70197 PubMed39968698
2025
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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