Rabbit Monoclonal Tafazzin / TAZ antibody. Carrier free. Suitable for IP, WB and reacts with Human, Rat, Mouse samples.
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
IP | Flow Cyt (Intra) | ICC/IF | IHC-P | WB | |
---|---|---|---|---|---|
Human | Tested | Not recommended | Not recommended | Not recommended | Tested |
Mouse | Expected | Not recommended | Not recommended | Not recommended | Tested |
Rat | Expected | Not recommended | Not recommended | Not recommended | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat, Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Human, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat, Mouse, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Rat, Mouse | Dilution info - | Notes - |
Acyltransferase which is required to maintain the composition of the phospholipid cardiolipin, a key component of the mitochondrial inner membrane (PubMed:12930833, PubMed:19700766, PubMed:19164547, PubMed:26908608, PubMed:33096711). Required for the initiation of mitophagy (PubMed:33096711). Required to ensure progression of spermatocytes through meiosis (By similarity).Isoform 5Catalytically inactive.Isoform 7Catalytically inactive.
Tafazzin, Protein G4.5, TAZ, G4.5, EFE2, TAFAZZIN
Rabbit Monoclonal Tafazzin / TAZ antibody. Carrier free. Suitable for IP, WB and reacts with Human, Rat, Mouse samples.
Tafazzin, Protein G4.5, TAZ, G4.5, EFE2, TAFAZZIN
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
Yes
EPR26956-58
Affinity purification Protein A
Blue Ice
+4°C
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
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.
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.
This supplementary information is collated from multiple sources and compiled automatically.
Tafazzin also known as TAZ is a mitochondrial phospholipid-lysophospholipid transacylase enzyme. It plays a role in the remodeling of cardiolipin a phospholipid found predominantly in the mitochondrial inner membrane. Tafazzin has a molecular mass of approximately 33 kDa. It is expressed in various tissues with higher expression levels found in tissues with high energy demands such as the heart and skeletal muscles.
Tafazzin is essential for maintaining mitochondrial function and energy production. It is a critical component of the system responsible for cardiolipin metabolism. The enzyme does not work alone; it interacts with other mitochondrial proteins to facilitate the proper composition of cardiolipin species necessary for mitochondrial structural integrity and functionality.
Tafazzin serves an important role in various lipid metabolism pathways. It participates in the phospholipid remodeling pathway where it interacts closely with acyltransferases to modify cardiolipin. This interaction is important for mitochondrial processes such as oxidative phosphorylation and energy conversion affecting proteins like cytochrome c oxidase and ATP synthase complex.
Tafazzin mutations are linked to Barth syndrome a rare genetic condition that affects the heart and muscles. This disorder is marked by symptoms including cardiomyopathy muscle weakness and neutropenia. Tafazzin dysfunction interrupts normal cardiolipin remodeling impacting proteins such as cytochrome c which contributes to abnormal energy metabolism seen in the syndrome. Additionally altered Tafazzin activity has connections to mitochondrial dysfunctions observed in some cardiomyopathies.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148, the same antibody clone in a different buffer formulation.
Tafazzin/TAZ was immunoprecipitated from 0.35 mg SW-13 (human adrenal gland; cortex epithelial cell) whole cell lysate 10 ug with Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution. Lane 1: SW-13 (human adrenal gland; cortex epithelial cell) whole cell lysate 10 ug
Lane 2: ABAB307148 IP in SW-13 whole cell lysate
Lane 3:RABbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148 in SW-13 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 180 seconds
All lanes: Immunoprecipitation - Anti-Tafazzin/TAZ antibody [EPR26956-58] (Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148) at 1/1000 dilution
Lane 1: SW-13 (human adrenal gland; cortex epithelial cell) whole cell lysate 10 μg
Lane 2: SW-13 whole cell lysate
Lane 3: Immunoprecipitation - Rabbit IgG, monoclonal [EPR25A] - Isotype Control (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730)
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution
Observed band size: 30 kDa
Exposure time: 180s
Tafazzin/TAZ was immunoprecipitated from 0.35 mg SW-13 (human adrenal gland; cortex epithelial cell) whole cell lysate 10 ug with Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution. Lane 1: SW-13 (human adrenal gland; cortex epithelial cell) whole cell lysate 10 ug
Lane 2: ABAB307148 IP in SW-13 whole cell lysate
Lane 3:RABbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148 in SW-13 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 180 seconds
This data was developed using 307148, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration:
Lanes 1, 4 and 5: 180 seconds, Lanes 2 and 3: 37 seconds
Exposure time:
All lanes: Western blot - Anti-Tafazzin/TAZ antibody [EPR26956-58] (Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148) at 1/1000 dilution
Lane 1: SW-13 (human adrenal gland; cortex epithelial cell) non-mitochondrial fraction 20 μg
Lane 2: SW-13 mitochondria fraction 20 μg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/50000 dilution
Observed band size: 30 kDa
Exposure time: 180s
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time: Lanes 1, 4 and 5: 180 seconds, Lanes 2 and 3: 37 seconds
This data was developed using 307148, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration:
180 seconds
Exposure time:
All lanes: Western blot - Anti-Tafazzin/TAZ antibody [EPR26956-58] (Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148) at 1/1000 dilution
Lane 1: Human colon cancer tissue lysate 20 μg
Lane 2: Mouse heart tissue lysate 20 μg
Lane 3: Mouse skeletal muscle tissue lysate 20 μg
Lane 4: Rat heart tissue lysate 20 μg
Lane 5: Rat skeletal muscle tissue lysate 20 μg
Lane 6: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate 20 μg
Lane 7: RAW 264.7 (mouse elson murine leukemia virus-induced tumor macrophage) whole cell lysate 20 μg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/50000 dilution
Observed band size: 30 kDa
Exposure time: 180s
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time: 180 seconds
This data was developed using 307148, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: This blot was developed using a high sensitivity ECL substrate.
180 seconds
Exposure time:
All lanes: Western blot - Anti-Tafazzin/TAZ antibody [EPR26956-58] (Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148) at 1/1000 dilution
Lane 1: HeLa (human cervical adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate 20 μg
Lane 2: HeLa transfected with siRNA specifically targeti Tafazzin/TAZ whole cell lysate 20 μg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/50000 dilution
Developed using the ECL technique.
Observed band size: 30 kDa
Exposure time: 180s
Blocking and diluting buffer and concentration: 5% NFDM/TBSTThis blot was developed using a high sensitivity ECL substrate.
Exposure time: 180 seconds
This data was developed using 307148, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: This blot was developed using a high sensitivity ECL substrate.
180 seconds
Exposure time:
All lanes: Western blot - Anti-Tafazzin/TAZ antibody [EPR26956-58] (Anti-Tafazzin/TAZ antibody [EPR26956-58] ab307148) at 1/1000 dilution
All lanes: HEK-293 (human embryonic kidney epithelial cell) whole cell lysate 20 μg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/50000 dilution
Developed using the ECL technique.
Observed band size: 30 kDa
Exposure time: 180s
Blocking and diluting buffer and concentration: 5% NFDM/TBSTThis blot was developed using a high sensitivity ECL substrate.
Exposure time: 180 seconds
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