Anti-MIRO1 antibody [CL1083] (ab188029) is a mouse monoclonal antibody that is used to detect MIRO1 in Western Blot, IHC-P. Suitable for Human samples.
- Specificity confirmed with MIRO1 knockout cell line validation
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine)
IHC-P | WB | |
---|---|---|
Human | Tested | Tested |
Mouse | Predicted | Predicted |
Rat | Predicted | Predicted |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/200.00000 - 1/500.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/500.00000 - 1/1000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
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Mitochondrial GTPase involved in mitochondrial trafficking (PubMed:12482879, PubMed:16630562, PubMed:22396657). Probably involved in control of anterograde transport of mitochondria and their subcellular distribution (PubMed:12482879, PubMed:16630562, PubMed:22396657). Promotes mitochondrial fission during high calcium conditions (PubMed:27716788).
ARHT1, RHOT1, Mitochondrial Rho GTPase 1, MIRO-1, hMiro-1, Rac-GTP-binding protein-like protein, Ras homolog gene family member T1
Anti-MIRO1 antibody [CL1083] (ab188029) is a mouse monoclonal antibody that is used to detect MIRO1 in Western Blot, IHC-P. Suitable for Human samples.
- Specificity confirmed with MIRO1 knockout cell line validation
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine)
MIRO1 also known as RhoT1 is a mitochondrial Rho GTPase with a molecular mass of approximately 69 kDa. It functions as a pivotal component in mitochondrial transport and dynamics. This protein localizes to the outer mitochondrial membrane and is highly expressed in various tissues particularly in the brain and muscles. MIRO1 facilitates the anchoring of mitochondria to microtubule motors enabling their movement within the cell which is essential for maintaining proper energy distribution.
MIRO1 plays a significant role in regulating mitochondrial trafficking along the cytoskeleton. It forms part of a protein complex with TRAK1/2 kinesin and dynein motor proteins. MIRO1's presence in this complex allows it to modulate mitochondrial distribution and dynamics which are essential for neural development and function. It also influences mitochondrial shape and interaction with the endoplasmic reticulum impacting intracellular calcium homeostasis.
MIRO1 is an integral component of pathways involving mitochondrial transport and cellular energy homeostasis. It actively participates in the regulation of calcium signaling pathways alongside related proteins like TRAK1. Additionally MIRO1's involvement in the maintenance of mitochondrial dynamics links it to mitophagy pathways. These pathways regulate the removal of damaged mitochondria a vital process for cellular health and longevity.
MIRO1 has connections to neurodegenerative conditions such as Parkinson's disease and Alzheimer's disease. These conditions correlate with impaired mitochondrial trafficking and dynamics. MIRO1 interacts with proteins such as PINK1 and Parkin which contribute to mitochondrial quality control and are involved in the pathogenesis of these diseases. The disruption of MIRO1 function can lead to mitochondrial dysfunction and energy deficits which are underlying factors in these neurodegenerative processes.
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False colour image of Western blot: Anti-MIRO1 antibody [CL1083] staining at 1/500 dilution, shown in green; Rabbit Anti-GAPDH antibody [EPR16891] (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab188029 was shown to bind specifically to MIRO1. A band was observed at 71 kDa in wild-type HeLa cell lysates with no signal observed at this size in RHOT1 knockout cell line Human RHOT1 (MIRO1) knockout HeLa cell line ab265792 (knockout cell lysate Human RHOT1 (MIRO1) knockout HeLa cell lysate ab258635). To generate this image, wild-type and RHOT1 knockout HeLa cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4°C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Mouse IgG H&L (IRDye® 800CW) preabsorbed (Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772) and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed (Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777) at 1/20000 dilution.
All lanes: Western blot - Anti-MIRO1 antibody [CL1083] (ab188029) at 1/500 dilution
Lane 1: Wild-type HeLa cell lysate at 40 µg
Lane 2: RHOT1 knockout HeLa cell lysate at 40 µg
Lane 2: Western blot - Human RHOT1 (MIRO1) knockout HeLa cell line (Human RHOT1 (MIRO1) knockout HeLa cell line ab265792)
Lane 3: HEK-293 cell lysate at 20 µg
Lane 4: A431 cell lysate at 20 µg
Performed under reducing conditions.
Predicted band size: 71 kDa
Observed band size: 71 kDa
All lanes: Western blot - Anti-MIRO1 antibody [CL1083] (ab188029) at 1/500 dilution
All lanes: Human cerebral cortex tissue
Predicted band size: 71 kDa
Immunohistochemical analysis of paraffin-embedded Human cerebellum tissue, labeling MIRO1 using ab188029 at a 1/200 dilution.
Immunohistochemical analysis of paraffin-embedded Human cerebral cortex tissue, labeling MIRO1 using ab188029 at a 1/200 dilution.
Immunohistochemical analysis of paraffin-embedded Human small intestine tissue, labeling MIRO1 using ab188029 at a 1/200 dilution.
Immunohistochemical analysis of paraffin-embedded Human liver tissue, labeling MIRO1 using ab188029 at a 1/200 dilution.
Immunohistochemical analysis of paraffin-embedded Human testis tissue, labeling MIRO1 using ab188029 at a 1/200 dilution.
Immunohistochemical analysis of paraffin-embedded Human breast cancer tissue, labeling MIRO1 using ab188029 at a 1/200 dilution.
Immunohistochemical analysis of paraffin-embedded Human stomach cancer tissue, labeling MIRO1 using ab188029 at a 1/200 dilution.
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