Rabbit Recombinant Monoclonal TIM44 antibody. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Rat samples. Cited in 1 publication.
View Alternative Names
MIMT44, TIM44, TIMM44, Mitochondrial import inner membrane translocase subunit TIM44
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-TIM44 antibody [EPR16821-26] (AB201453)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HepG2 (Human liver hepatocellular carcinoma) cells labeling TIM44 with ab201453 at 1/500 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing cytoplasm staining on HepG2 cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab201453 at 1/500 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-TIM44 antibody [EPR16821-26] (AB201453)
Intracellular Flow Cytometry analysis of HepG2 (human hepatocellular carcinoma) labelling TIM44 with purified ab201453 at 1/500 (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Alexa Fluor® 488 goat anti-rabbit IgG (1/2000) was used as the secondary antibody. Black - Isotype control, rabbit monoclonal IgG. Blue - Unlabelled control, cells without incubation with primary and secondary antibodies.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-TIM44 antibody [EPR16821-26] (AB201453)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized K562 (Human chronic myelogenous leukemia cells from bone marrow) cells labeling TIM44 with ab201453 at 1/500 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing cytoplasm staining on K562 cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab201453 at 1/500 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- WB
Supplier Data
Western blot - Anti-TIM44 antibody [EPR16821-26] (AB201453)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-TIM44 antibody [EPR16821-26] (ab201453) at 1/10000 dilution
All lanes:
Human fetal liver lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 51 kDa
Observed band size: 45 kDa
false
Exposure time: 3min
- IP
Supplier Data
Immunoprecipitation - Anti-TIM44 antibody [EPR16821-26] (AB201453)
TIM44 was immunoprecipitated from 1mg of K562 (Human chronic myelogenous leukemia cells from bone marrow) whole cell lysate with ab201453 at 1/120 dilution. Western blot was performed from the immunoprecipitate using ab201453 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/1500 dilution.
Lane 1 : K562 whole cell lysate 10 μg (Input). Lane 2 : ab201453 IP in K562 whole cell lysate. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab201453 in K562 whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 1 second.
All lanes:
Immunoprecipitation - Anti-TIM44 antibody [EPR16821-26] (ab201453)
Predicted band size: 51 kDa
false
- WB
Supplier Data
Western blot - Anti-TIM44 antibody [EPR16821-26] (AB201453)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-TIM44 antibody [EPR16821-26] (ab201453) at 1/2000 dilution
Lane 1:
K562 (Human chronic myelogenous leukemia cells from bone marrow) cell lysate at 20 µg
Lane 2:
HepG2 (Human liver hepatocellular carcinoma) cell lysate at 20 µg
Lane 3:
Daudi (Human Burkitt's lymphoma cell line) cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 51 kDa
Observed band size: 45 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-TIM44 antibody [EPR16821-26] (AB201453)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-TIM44 antibody [EPR16821-26] (ab201453) at 1/2000 dilution
Lane 1:
C6 (Rat glial tumor cells) cell lysate at 10 µg
Lane 2:
PC-12 (Rat adrenal gland pheochromocytoma) cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 51 kDa
Observed band size: 45 kDa
false
Exposure time: 3min
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
TIM44 functions in conjunction with other components of the TIM23 complex which includes proteins like TIM23 and TIM17. The main role of TIM44 involves connecting the translocase complex to mitochondrial heat shock protein 70 (mtHsp70) facilitating ATP-dependent translocation of polypeptides. This process supports the import of precursor proteins synthesized in the cytosol into the mitochondria ensuring proper mitochondrial function and energy production.
Pathways
TIM44 influences the mitochondrial protein import pathway and the maintenance of mitochondrial function. As part of the protein import machinery it connects closely to the chaperone-mediated folding pathway aided by mtHsp70. The TIM23 complex participates in the translocation of proteins with mitochondrial targeting sequences linking TIM44 to pathways essential for mitochondrial biogenesis and function.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
The Journal of biological chemistry 300:107958 PubMed39510176
2024
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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