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anti tom20  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti tom20
    Anti Tom20, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 255 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tom20/BNIP3L%2FNix+Rabbit+mAb/pmc13049664-189-26-27
    Average 96 stars, based on 255 article reviews
    anti tom20 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Incubation:

    Article Title: COX5A induces M2 macrophage polarization in chronic rhinosinusitis with nasal polyps through ROS generation
    Article Snippet: For HE staining, the tissues were stained with the commercial HE kit (Beyotime, C0105M) according to the manufacturer’s instructions. .. After boiling in a citric acid buffer (Servicebio, G1202) for antigen recovery, the tissue sections were blocked with 5% Bovine Serum Albumin (BSA) (Beyotime, P0023B) in TBST (Servicebio, G0001) and then incubated with primary antibodies against CD206(1:400,Cell Signaling Technology (CST), 24595), COX5A (1:500, ABclonal, A6437), and TOM20 (1:400, CST, 42406), followed by secondary antibody incubationThe slides were then washed, counterstained with DAPI. .. For multiplex tissue fluorescence, slides were incubated with detection reagent (AFIHC034, AIFang biological) in a humidified, light-protected environment for 30 minutes.

    Article Title: Blockade of T-type Ca2+ channels disrupts mitochondrial function and follicle development by inhibiting the PI3K/AKT pathway.
    Article Snippet: Calcium (Ca2+) function as critical secondary messengers in cellular signaling, essential for maintaining ovarian function and promoting oocyte maturation.. However, the contribution of T-type voltage-gated calcium channels (VGCCs) to ovarian follicle development remains unclear.. To investigate this, we administered flunarizine (FNZ), a potent T-type VGCCs antagonist, to 4-6-week-old female mice via intraperitoneal injection at doses of 0, 3, or 30 mg/kg/day for 7 days.

    Article Title: Onconase Induces Apoptosis in Dabrafenib-Resistant Melanoma Cell Lines Through Dysregulation of ROS Homeostasis, Antioxidant Protein Expression, and Mitochondrial Dynamics.
    Article Snippet: Protein extracts were separated by SDS–PAGE using 8.5–14% polyacrylamide gels, and subsequently transferred onto polyvinylidene difluoride (PVDF) membranes (Merck Millipore, Milan, Italy), blocked for 1 h at RT in TBST buffer (10 mM Tris-HCl, pH 7.5; 100 mM NaCl; 0.1% Tween 20) containing 5% non-fat milk. .. Membranes were then incubated overnight at 4 ◦C with gentle agitation in 5% bovine serum albumin (BSA) containing the following primary antibodies: FTH1 (A19544); p(Ser40)-NRF2 (AP1133); HO-1 (A19062); GCLM (A11444); SLC7A11 (A2413); GSTP1 (A19061); FSP1 (A22278); cleaved PARP (A19612); LC3B (AA19665); p(T161)CDK1 (AP0324); p(Thr160)CDK2 (AP1364); p(Thr172)CDK4 (AP1364); p(ser616)-DRP1 (AP1353); FIS1 (A19666); PINK1 (A24745); ATPB (A11214); pERK1/2 (AP0974); ERK1/2 (A16686); UQCRC1 (A26343); (Abclonal, Woburn, MA, USA); ATG3 (GTX128065); Beclin1 (GTX133555); SOD2 (GTX630559); Glutathione reductase (GTX114199); COX4 (GTX114330); c-Myc (GTX103436); (GeneTex, Irvine, CA, USA); Mitofusin-1 (#14739); Mitofusin-2 (#11925); DRP1 (#8570); OPA1 (#80471); TOM20 (#42406); GAPDH (#2118); p(Tyr605)-STAT3 (#9145); p(Ser536)P65-NF-kB (#3033); cleaved Caspase 9 (#9509) (Cell Signaling Technology, Danvers, MA, USA); PGC1α (PA5-38022) (Invitrogen, Life Technologies, Monza, Italy); γ-H2AX (29380-1); Survivin (66495-1-Ig); and β-actin (66031-1) (Proteintech, Manchester, UK). .. After primary antibody incubation, membranes were washed three times for 10 min each with TBST and then incubated for 1 h at RT with horseradish peroxidase (HRP)-conjugated anti-rabbit or anti-mouse secondary https://doi.org/10.3390/ijms27041638 antibodies (Cell Signaling Technology, Danvers, MA, USA).

    Article Title: COX5A induces M2 macrophage polarization in chronic rhinosinusitis with nasal polyps through ROS generation.
    Article Snippet: For HE staining, the tissues were stained with the commercial HE kit (Beyotime, C0105M) according to the manufacturer’s instructions. .. Immunofluorescence(mIF) After boiling in a citric acid buffer (Servicebio, G1202) for antigen recovery, the tissue sections were blocked with 5% Bovine Serum Albumin (BSA) (Beyotime, P0023B) in TBST (Servicebio, G0001) and then incubated with primary antibodies against CD206(1:400,Cell Signaling Technology (CST), 24595), COX5A (1:500, ABclonal, A6437), and TOM20 (1:400, CST, 42406), followed by secondary antibody incubationThe slides were then washed, counterstained with DAPI. .. For multiplex tissue fluorescence, slides were incubated with detection reagent (AFIHC034, AIFang biological) in a humidified, light-protected environment for 30 minutes.

    Western Blot:

    Article Title: Parkinson's disease-associated PLA2G6 protects IP3R1 protein to control ER-mitochondria tethering and Ca 2+ transfer.
    Article Snippet: Immunoblotting signals were detected using a chemiluminescence reagent (Invitrogen, 32106) and quantified via ImageJ. .. The antibodies used for immunoblotting included PLA2G6 (Abcam, ab259950, 1:1000), GRP75 (Santa Cruz, sc-133137, 1:500), VDAC1 (Proteintech, 55259-1-AP, 1:1000), Sigma1R (CST, 61994, 1:1000), COX IV (ABclonal, A11631, 1:1000), Calreticulin (ABclonal, A20986, 1:1000), IP3R1 (ABclonal, A21471, 1:1000), MFN2 (Abcam, ab124773, 1:1000), TOM40 (ABclonal, A3213, 1:1000), TOM20 (CST, 42406S, AR TI CL E IN P RE SS 1:1000), TIM23 (Proteintech, 11123-1-AP, 1:1000), ubiquitin (Santa Cruz, sc-8017, 1:500), ERLIN2 (ABclonal, A0781, 1:1000), NDUFA9 (ABclonal, A3196, 1:1000), pS129 (CST, 23706, 1:1000), GSK3β (ABclonal, A2081, 1:1000), DJ-1 (Proteintech, 68915-6-Ig, 1:1000), GFP (HUABIO, ET1607-31, 1:2000), LAMP1 (Santa Cruz, sc-20011, 1:500) and GAPDH (Proteintech, 60004-1-Ig, 1:5000). .. For Co-IP assays, proteins were extracted from cells and mouse ventral midbrains using 1% NP-40 lysis buffer (Beyotime, P0013F) supplemented with a protease inhibitor cocktail (MCE, HY-K0010) on ice for 30 minutes.

    Article Title: ER-localized ceramide accumulation contributes to replicative senescence.
    Article Snippet: Article ER-localized ceramide accumulation contributes to replicative senescence

    Ubiquitin Proteomics:

    Article Title: Parkinson's disease-associated PLA2G6 protects IP3R1 protein to control ER-mitochondria tethering and Ca 2+ transfer.
    Article Snippet: Immunoblotting signals were detected using a chemiluminescence reagent (Invitrogen, 32106) and quantified via ImageJ. .. The antibodies used for immunoblotting included PLA2G6 (Abcam, ab259950, 1:1000), GRP75 (Santa Cruz, sc-133137, 1:500), VDAC1 (Proteintech, 55259-1-AP, 1:1000), Sigma1R (CST, 61994, 1:1000), COX IV (ABclonal, A11631, 1:1000), Calreticulin (ABclonal, A20986, 1:1000), IP3R1 (ABclonal, A21471, 1:1000), MFN2 (Abcam, ab124773, 1:1000), TOM40 (ABclonal, A3213, 1:1000), TOM20 (CST, 42406S, AR TI CL E IN P RE SS 1:1000), TIM23 (Proteintech, 11123-1-AP, 1:1000), ubiquitin (Santa Cruz, sc-8017, 1:500), ERLIN2 (ABclonal, A0781, 1:1000), NDUFA9 (ABclonal, A3196, 1:1000), pS129 (CST, 23706, 1:1000), GSK3β (ABclonal, A2081, 1:1000), DJ-1 (Proteintech, 68915-6-Ig, 1:1000), GFP (HUABIO, ET1607-31, 1:2000), LAMP1 (Santa Cruz, sc-20011, 1:500) and GAPDH (Proteintech, 60004-1-Ig, 1:5000). .. For Co-IP assays, proteins were extracted from cells and mouse ventral midbrains using 1% NP-40 lysis buffer (Beyotime, P0013F) supplemented with a protease inhibitor cocktail (MCE, HY-K0010) on ice for 30 minutes.

    Article Title: USP30 alleviates intestinal ischemia-reperfusion injury by deubiquitinating MFN2 mediating the mitochondrial endoplasmic reticulum pathway.
    Article Snippet: Intestinal ischemia-reperfusion (IIR) injury can cause intestinal barrier damage, systemic inflammatory response, and high mortality.. The key mechanism is the disorder of the mitochondrial-endoplasmic reticulum network.. Ubiquitin-specific peptidase 30 (USP30), located on the outer mitochondrial membrane, can reverse the partial ubiquitination of Parkin substrates or completely remove the ubiquitin chain to maintain mitochondrial function.

    Membrane:

    Article Title: Blockade of T-type Ca2+ channels disrupts mitochondrial function and follicle development by inhibiting the PI3K/AKT pathway.
    Article Snippet: Calcium (Ca2+) function as critical secondary messengers in cellular signaling, essential for maintaining ovarian function and promoting oocyte maturation.. However, the contribution of T-type voltage-gated calcium channels (VGCCs) to ovarian follicle development remains unclear.. To investigate this, we administered flunarizine (FNZ), a potent T-type VGCCs antagonist, to 4-6-week-old female mice via intraperitoneal injection at doses of 0, 3, or 30 mg/kg/day for 7 days.

    Gentle:

    Article Title: Onconase Induces Apoptosis in Dabrafenib-Resistant Melanoma Cell Lines Through Dysregulation of ROS Homeostasis, Antioxidant Protein Expression, and Mitochondrial Dynamics.
    Article Snippet: Protein extracts were separated by SDS–PAGE using 8.5–14% polyacrylamide gels, and subsequently transferred onto polyvinylidene difluoride (PVDF) membranes (Merck Millipore, Milan, Italy), blocked for 1 h at RT in TBST buffer (10 mM Tris-HCl, pH 7.5; 100 mM NaCl; 0.1% Tween 20) containing 5% non-fat milk. .. Membranes were then incubated overnight at 4 ◦C with gentle agitation in 5% bovine serum albumin (BSA) containing the following primary antibodies: FTH1 (A19544); p(Ser40)-NRF2 (AP1133); HO-1 (A19062); GCLM (A11444); SLC7A11 (A2413); GSTP1 (A19061); FSP1 (A22278); cleaved PARP (A19612); LC3B (AA19665); p(T161)CDK1 (AP0324); p(Thr160)CDK2 (AP1364); p(Thr172)CDK4 (AP1364); p(ser616)-DRP1 (AP1353); FIS1 (A19666); PINK1 (A24745); ATPB (A11214); pERK1/2 (AP0974); ERK1/2 (A16686); UQCRC1 (A26343); (Abclonal, Woburn, MA, USA); ATG3 (GTX128065); Beclin1 (GTX133555); SOD2 (GTX630559); Glutathione reductase (GTX114199); COX4 (GTX114330); c-Myc (GTX103436); (GeneTex, Irvine, CA, USA); Mitofusin-1 (#14739); Mitofusin-2 (#11925); DRP1 (#8570); OPA1 (#80471); TOM20 (#42406); GAPDH (#2118); p(Tyr605)-STAT3 (#9145); p(Ser536)P65-NF-kB (#3033); cleaved Caspase 9 (#9509) (Cell Signaling Technology, Danvers, MA, USA); PGC1α (PA5-38022) (Invitrogen, Life Technologies, Monza, Italy); γ-H2AX (29380-1); Survivin (66495-1-Ig); and β-actin (66031-1) (Proteintech, Manchester, UK). .. After primary antibody incubation, membranes were washed three times for 10 min each with TBST and then incubated for 1 h at RT with horseradish peroxidase (HRP)-conjugated anti-rabbit or anti-mouse secondary https://doi.org/10.3390/ijms27041638 antibodies (Cell Signaling Technology, Danvers, MA, USA).

    Immunofluorescence:

    Article Title: COX5A induces M2 macrophage polarization in chronic rhinosinusitis with nasal polyps through ROS generation.
    Article Snippet: For HE staining, the tissues were stained with the commercial HE kit (Beyotime, C0105M) according to the manufacturer’s instructions. .. Immunofluorescence(mIF) After boiling in a citric acid buffer (Servicebio, G1202) for antigen recovery, the tissue sections were blocked with 5% Bovine Serum Albumin (BSA) (Beyotime, P0023B) in TBST (Servicebio, G0001) and then incubated with primary antibodies against CD206(1:400,Cell Signaling Technology (CST), 24595), COX5A (1:500, ABclonal, A6437), and TOM20 (1:400, CST, 42406), followed by secondary antibody incubationThe slides were then washed, counterstained with DAPI. .. For multiplex tissue fluorescence, slides were incubated with detection reagent (AFIHC034, AIFang biological) in a humidified, light-protected environment for 30 minutes.



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    The origin of the sperm, control, or oligoasthenospermic influence the mitochondrial area. (A) Representative images obtained by immunofluorescence staining of spermatozoa with typical morphology. (B) An example of atypical morphology of spermatozoa with defects in the head and middle piece. Mitochondria were immunostained by <t>anti‐TOM20</t> antibodies (orange), scale bar = 1 µm. (C) Representative images of the probes MitoTracker Green, the blue dots delimited the head of the spermatozoon, scale bar = 1 µm. (D) Mitochondrial area assessed by TOM20. Results are presented with a box‐and‐whiskers plot, each box represents the interquartile range (25th–75th percentile), with the horizontal line indicating the median. Whiskers extend to the maximum from the minimum. Total control (Ct) n = 760 spermatozoa; Total oligoasthenospermic (OA) n = 612; Typical Ct n = 179; Atypical Ct n = 581; Typical OA n = 118; Atypical OA n = 494. The p‐ value of the two‐sided permutation t‐test is represented as * p < 0.05; ** p ≤ 0.01; *** p ≤ 0.001.
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    The origin of the sperm, control, or oligoasthenospermic influence the mitochondrial area. (A) Representative images obtained by immunofluorescence staining of spermatozoa with typical morphology. (B) An example of atypical morphology of spermatozoa with defects in the head and middle piece. Mitochondria were immunostained by <t>anti‐TOM20</t> antibodies (orange), scale bar = 1 µm. (C) Representative images of the probes MitoTracker Green, the blue dots delimited the head of the spermatozoon, scale bar = 1 µm. (D) Mitochondrial area assessed by TOM20. Results are presented with a box‐and‐whiskers plot, each box represents the interquartile range (25th–75th percentile), with the horizontal line indicating the median. Whiskers extend to the maximum from the minimum. Total control (Ct) n = 760 spermatozoa; Total oligoasthenospermic (OA) n = 612; Typical Ct n = 179; Atypical Ct n = 581; Typical OA n = 118; Atypical OA n = 494. The p‐ value of the two‐sided permutation t‐test is represented as * p < 0.05; ** p ≤ 0.01; *** p ≤ 0.001.
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    Image Search Results


    The origin of the sperm, control, or oligoasthenospermic influence the mitochondrial area. (A) Representative images obtained by immunofluorescence staining of spermatozoa with typical morphology. (B) An example of atypical morphology of spermatozoa with defects in the head and middle piece. Mitochondria were immunostained by anti‐TOM20 antibodies (orange), scale bar = 1 µm. (C) Representative images of the probes MitoTracker Green, the blue dots delimited the head of the spermatozoon, scale bar = 1 µm. (D) Mitochondrial area assessed by TOM20. Results are presented with a box‐and‐whiskers plot, each box represents the interquartile range (25th–75th percentile), with the horizontal line indicating the median. Whiskers extend to the maximum from the minimum. Total control (Ct) n = 760 spermatozoa; Total oligoasthenospermic (OA) n = 612; Typical Ct n = 179; Atypical Ct n = 581; Typical OA n = 118; Atypical OA n = 494. The p‐ value of the two‐sided permutation t‐test is represented as * p < 0.05; ** p ≤ 0.01; *** p ≤ 0.001.

    Journal: Molecular Reproduction and Development

    Article Title: High‐Resolution Imaging Reveals Mitochondrial Protein Imbalance in Sperm of Oligoasthenospermic Men

    doi: 10.1002/mrd.70110

    Figure Lengend Snippet: The origin of the sperm, control, or oligoasthenospermic influence the mitochondrial area. (A) Representative images obtained by immunofluorescence staining of spermatozoa with typical morphology. (B) An example of atypical morphology of spermatozoa with defects in the head and middle piece. Mitochondria were immunostained by anti‐TOM20 antibodies (orange), scale bar = 1 µm. (C) Representative images of the probes MitoTracker Green, the blue dots delimited the head of the spermatozoon, scale bar = 1 µm. (D) Mitochondrial area assessed by TOM20. Results are presented with a box‐and‐whiskers plot, each box represents the interquartile range (25th–75th percentile), with the horizontal line indicating the median. Whiskers extend to the maximum from the minimum. Total control (Ct) n = 760 spermatozoa; Total oligoasthenospermic (OA) n = 612; Typical Ct n = 179; Atypical Ct n = 581; Typical OA n = 118; Atypical OA n = 494. The p‐ value of the two‐sided permutation t‐test is represented as * p < 0.05; ** p ≤ 0.01; *** p ≤ 0.001.

    Article Snippet: The resulting surface accurately reflected the size and shape of the TOM20 immunolabeling intensity distribution as detected by Imaris.

    Techniques: Control, Immunofluorescence, Staining