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proteintech rabbit polyclonal txnl6  (Proteintech)


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    Structured Review

    Proteintech proteintech rabbit polyclonal txnl6
    Ethidium bromide stained agarose gels show Panel A - <t>TXNL6,</t> Panel B - Trx 1, Panel C - Trx 2 and Panel D GAPDH (control) transcript from 200 ng of RNA obtained from human tissues - 1. Lens epithelium, 2. Lens Fiber, 3. Retina, 4. Stomach, 5. Kidney, 6.Heart, 7. Colon, and 8. Spleen.
    Proteintech Rabbit Polyclonal Txnl6, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/proteintech rabbit polyclonal txnl6/product/Proteintech
    Average 93 stars, based on 2 article reviews
    proteintech rabbit polyclonal txnl6 - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens"

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0015421

    Ethidium bromide stained agarose gels show Panel A - TXNL6, Panel B - Trx 1, Panel C - Trx 2 and Panel D GAPDH (control) transcript from 200 ng of RNA obtained from human tissues - 1. Lens epithelium, 2. Lens Fiber, 3. Retina, 4. Stomach, 5. Kidney, 6.Heart, 7. Colon, and 8. Spleen.
    Figure Legend Snippet: Ethidium bromide stained agarose gels show Panel A - TXNL6, Panel B - Trx 1, Panel C - Trx 2 and Panel D GAPDH (control) transcript from 200 ng of RNA obtained from human tissues - 1. Lens epithelium, 2. Lens Fiber, 3. Retina, 4. Stomach, 5. Kidney, 6.Heart, 7. Colon, and 8. Spleen.

    Techniques Used: Staining

    SDS-PAGE and immunoblotting of microdissected lens epithelium (Epi) and lens fiber cell total protein extracts (20 µg) with a TXNL6-specific antibody.
    Figure Legend Snippet: SDS-PAGE and immunoblotting of microdissected lens epithelium (Epi) and lens fiber cell total protein extracts (20 µg) with a TXNL6-specific antibody.

    Techniques Used: SDS Page, Western Blot

    SDS-PAGE and immunoblotting of Panel A - TXNL6, Panel B - MsrA, Panel C - Trx 1, and Panel D -Trx 2 in 5 µg of protein extracts from the cytoplasm and mitochondria of HLE-B3 lens epithelial cells using specific antibodies.
    Figure Legend Snippet: SDS-PAGE and immunoblotting of Panel A - TXNL6, Panel B - MsrA, Panel C - Trx 1, and Panel D -Trx 2 in 5 µg of protein extracts from the cytoplasm and mitochondria of HLE-B3 lens epithelial cells using specific antibodies.

    Techniques Used: SDS Page, Western Blot

    Co-localization of Panel A - TXNL6 (green), Panel B - Trx 1 (green) and Panel C - Trx 2 (green), mitotracker red – a specific mitochondrial marker and merging of the two images (orange/yellow) in HLE-B3 lens epithelial cells by immunofluoresence microscopy.
    Figure Legend Snippet: Co-localization of Panel A - TXNL6 (green), Panel B - Trx 1 (green) and Panel C - Trx 2 (green), mitotracker red – a specific mitochondrial marker and merging of the two images (orange/yellow) in HLE-B3 lens epithelial cells by immunofluoresence microscopy.

    Techniques Used: Marker, Microscopy

    A. Ethidium bromide stained agarose gels showing TXNL6 and control GAPDH transcript levels in 200 ng RNA isolated from HLE-B3 human lens epithelial cells at 0, 30 min, 6 h and 16 h recovery following a 2 h exposure to 200 µM H 2 O 2 . B. Western blot showing TXNL6 protein levels in 5 µg of total protein extract isolated from HLE-B3 lens epithelial cells at 0, 6 h, 16 h and 24 h recovery following a 2 h exposure to 200 µM H 2 O 2 . The coomassie blue stained SDS-PAGE gel is shown as a control for equal protein loading.
    Figure Legend Snippet: A. Ethidium bromide stained agarose gels showing TXNL6 and control GAPDH transcript levels in 200 ng RNA isolated from HLE-B3 human lens epithelial cells at 0, 30 min, 6 h and 16 h recovery following a 2 h exposure to 200 µM H 2 O 2 . B. Western blot showing TXNL6 protein levels in 5 µg of total protein extract isolated from HLE-B3 lens epithelial cells at 0, 6 h, 16 h and 24 h recovery following a 2 h exposure to 200 µM H 2 O 2 . The coomassie blue stained SDS-PAGE gel is shown as a control for equal protein loading.

    Techniques Used: Staining, Isolation, Western Blot, SDS Page

    Representative graph (from 3 independent experiments) of cytochrome c (cyt c) mediated peroxidase activity. The graph shows mean values for an N of 3 ± SD. Cyt c oxidized (cyt c ox) (incubated for 15 min with a 4∶1 molar ratio of HOCl) is 100% peroxidase activity, all other activities are expressed as a percentage of the cyt c ox activity. The untreated cyt c protein has 16% cyt c peroxidase activity compared to cyt c ox. Cyt c ox incubated with MsrA in the absence of a reducing system has 91% activity of the oxidized. Treatment of the cyt c ox (291 µM) with MsrA (1.9 µM for 2 h at 37°C) and TXNL6 (1.39 µM) with thioredoxin reductase (TxrR) and NADPH leads to a statistically significant (p<0.001) 48% decrease in peroxidase activity. Similarly treatment of cyt c ox with MsrA and either Trx 1 or Trx 2 (both 1.39 µM) with TxrR/NADPH also significantly (p<0.001) decreased both peroxidase activities by 52% and 54% respectively. Incubation of cyt c ox with MsrA and TXNL6 in the absence of TxrR/NADPH resulted in just a 14% decrease in cyt c peroxidase activity while incubation of cyt c ox with TXNL6 and TxrR/NADPH in the absence of MsrA resulted in 19% decrease in cyt c peroxidase activity. p values were obtained using Tukey's test following one-way ANOVA.
    Figure Legend Snippet: Representative graph (from 3 independent experiments) of cytochrome c (cyt c) mediated peroxidase activity. The graph shows mean values for an N of 3 ± SD. Cyt c oxidized (cyt c ox) (incubated for 15 min with a 4∶1 molar ratio of HOCl) is 100% peroxidase activity, all other activities are expressed as a percentage of the cyt c ox activity. The untreated cyt c protein has 16% cyt c peroxidase activity compared to cyt c ox. Cyt c ox incubated with MsrA in the absence of a reducing system has 91% activity of the oxidized. Treatment of the cyt c ox (291 µM) with MsrA (1.9 µM for 2 h at 37°C) and TXNL6 (1.39 µM) with thioredoxin reductase (TxrR) and NADPH leads to a statistically significant (p<0.001) 48% decrease in peroxidase activity. Similarly treatment of cyt c ox with MsrA and either Trx 1 or Trx 2 (both 1.39 µM) with TxrR/NADPH also significantly (p<0.001) decreased both peroxidase activities by 52% and 54% respectively. Incubation of cyt c ox with MsrA and TXNL6 in the absence of TxrR/NADPH resulted in just a 14% decrease in cyt c peroxidase activity while incubation of cyt c ox with TXNL6 and TxrR/NADPH in the absence of MsrA resulted in 19% decrease in cyt c peroxidase activity. p values were obtained using Tukey's test following one-way ANOVA.

    Techniques Used: Activity Assay, Incubation

    Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized cyt c (5 µg). Lane 1 untreated cyt c cleaved with CNBr. Lane 2 Oxidized cyt c (0.2 mM oxidized with 0.8 mM HOCl; a 4∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.
    Figure Legend Snippet: Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized cyt c (5 µg). Lane 1 untreated cyt c cleaved with CNBr. Lane 2 Oxidized cyt c (0.2 mM oxidized with 0.8 mM HOCl; a 4∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.

    Techniques Used: Staining, SDS Page

    Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized α-crystallin (5 µg). Lane 1 untreated α-crystallin cleaved with CNBr. Lane 2 Oxidized α-crystallin (9.09 µM oxidized with 909 µm HOCl; a 100∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. Lane 5 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (20 µg; 2.78 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.
    Figure Legend Snippet: Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized α-crystallin (5 µg). Lane 1 untreated α-crystallin cleaved with CNBr. Lane 2 Oxidized α-crystallin (9.09 µM oxidized with 909 µm HOCl; a 100∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. Lane 5 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (20 µg; 2.78 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.

    Techniques Used: Staining, SDS Page



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    Proteintech proteintech rabbit polyclonal txnl6
    Ethidium bromide stained agarose gels show Panel A - <t>TXNL6,</t> Panel B - Trx 1, Panel C - Trx 2 and Panel D GAPDH (control) transcript from 200 ng of RNA obtained from human tissues - 1. Lens epithelium, 2. Lens Fiber, 3. Retina, 4. Stomach, 5. Kidney, 6.Heart, 7. Colon, and 8. Spleen.
    Proteintech Rabbit Polyclonal Txnl6, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/proteintech rabbit polyclonal txnl6/product/Proteintech
    Average 93 stars, based on 1 article reviews
    proteintech rabbit polyclonal txnl6 - by Bioz Stars, 2026-02
    93/100 stars
      Buy from Supplier

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    Ethidium bromide stained agarose gels show Panel A - TXNL6, Panel B - Trx 1, Panel C - Trx 2 and Panel D GAPDH (control) transcript from 200 ng of RNA obtained from human tissues - 1. Lens epithelium, 2. Lens Fiber, 3. Retina, 4. Stomach, 5. Kidney, 6.Heart, 7. Colon, and 8. Spleen.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: Ethidium bromide stained agarose gels show Panel A - TXNL6, Panel B - Trx 1, Panel C - Trx 2 and Panel D GAPDH (control) transcript from 200 ng of RNA obtained from human tissues - 1. Lens epithelium, 2. Lens Fiber, 3. Retina, 4. Stomach, 5. Kidney, 6.Heart, 7. Colon, and 8. Spleen.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: Staining

    SDS-PAGE and immunoblotting of microdissected lens epithelium (Epi) and lens fiber cell total protein extracts (20 µg) with a TXNL6-specific antibody.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: SDS-PAGE and immunoblotting of microdissected lens epithelium (Epi) and lens fiber cell total protein extracts (20 µg) with a TXNL6-specific antibody.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: SDS Page, Western Blot

    SDS-PAGE and immunoblotting of Panel A - TXNL6, Panel B - MsrA, Panel C - Trx 1, and Panel D -Trx 2 in 5 µg of protein extracts from the cytoplasm and mitochondria of HLE-B3 lens epithelial cells using specific antibodies.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: SDS-PAGE and immunoblotting of Panel A - TXNL6, Panel B - MsrA, Panel C - Trx 1, and Panel D -Trx 2 in 5 µg of protein extracts from the cytoplasm and mitochondria of HLE-B3 lens epithelial cells using specific antibodies.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: SDS Page, Western Blot

    Co-localization of Panel A - TXNL6 (green), Panel B - Trx 1 (green) and Panel C - Trx 2 (green), mitotracker red – a specific mitochondrial marker and merging of the two images (orange/yellow) in HLE-B3 lens epithelial cells by immunofluoresence microscopy.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: Co-localization of Panel A - TXNL6 (green), Panel B - Trx 1 (green) and Panel C - Trx 2 (green), mitotracker red – a specific mitochondrial marker and merging of the two images (orange/yellow) in HLE-B3 lens epithelial cells by immunofluoresence microscopy.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: Marker, Microscopy

    A. Ethidium bromide stained agarose gels showing TXNL6 and control GAPDH transcript levels in 200 ng RNA isolated from HLE-B3 human lens epithelial cells at 0, 30 min, 6 h and 16 h recovery following a 2 h exposure to 200 µM H 2 O 2 . B. Western blot showing TXNL6 protein levels in 5 µg of total protein extract isolated from HLE-B3 lens epithelial cells at 0, 6 h, 16 h and 24 h recovery following a 2 h exposure to 200 µM H 2 O 2 . The coomassie blue stained SDS-PAGE gel is shown as a control for equal protein loading.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: A. Ethidium bromide stained agarose gels showing TXNL6 and control GAPDH transcript levels in 200 ng RNA isolated from HLE-B3 human lens epithelial cells at 0, 30 min, 6 h and 16 h recovery following a 2 h exposure to 200 µM H 2 O 2 . B. Western blot showing TXNL6 protein levels in 5 µg of total protein extract isolated from HLE-B3 lens epithelial cells at 0, 6 h, 16 h and 24 h recovery following a 2 h exposure to 200 µM H 2 O 2 . The coomassie blue stained SDS-PAGE gel is shown as a control for equal protein loading.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: Staining, Isolation, Western Blot, SDS Page

    Representative graph (from 3 independent experiments) of cytochrome c (cyt c) mediated peroxidase activity. The graph shows mean values for an N of 3 ± SD. Cyt c oxidized (cyt c ox) (incubated for 15 min with a 4∶1 molar ratio of HOCl) is 100% peroxidase activity, all other activities are expressed as a percentage of the cyt c ox activity. The untreated cyt c protein has 16% cyt c peroxidase activity compared to cyt c ox. Cyt c ox incubated with MsrA in the absence of a reducing system has 91% activity of the oxidized. Treatment of the cyt c ox (291 µM) with MsrA (1.9 µM for 2 h at 37°C) and TXNL6 (1.39 µM) with thioredoxin reductase (TxrR) and NADPH leads to a statistically significant (p<0.001) 48% decrease in peroxidase activity. Similarly treatment of cyt c ox with MsrA and either Trx 1 or Trx 2 (both 1.39 µM) with TxrR/NADPH also significantly (p<0.001) decreased both peroxidase activities by 52% and 54% respectively. Incubation of cyt c ox with MsrA and TXNL6 in the absence of TxrR/NADPH resulted in just a 14% decrease in cyt c peroxidase activity while incubation of cyt c ox with TXNL6 and TxrR/NADPH in the absence of MsrA resulted in 19% decrease in cyt c peroxidase activity. p values were obtained using Tukey's test following one-way ANOVA.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: Representative graph (from 3 independent experiments) of cytochrome c (cyt c) mediated peroxidase activity. The graph shows mean values for an N of 3 ± SD. Cyt c oxidized (cyt c ox) (incubated for 15 min with a 4∶1 molar ratio of HOCl) is 100% peroxidase activity, all other activities are expressed as a percentage of the cyt c ox activity. The untreated cyt c protein has 16% cyt c peroxidase activity compared to cyt c ox. Cyt c ox incubated with MsrA in the absence of a reducing system has 91% activity of the oxidized. Treatment of the cyt c ox (291 µM) with MsrA (1.9 µM for 2 h at 37°C) and TXNL6 (1.39 µM) with thioredoxin reductase (TxrR) and NADPH leads to a statistically significant (p<0.001) 48% decrease in peroxidase activity. Similarly treatment of cyt c ox with MsrA and either Trx 1 or Trx 2 (both 1.39 µM) with TxrR/NADPH also significantly (p<0.001) decreased both peroxidase activities by 52% and 54% respectively. Incubation of cyt c ox with MsrA and TXNL6 in the absence of TxrR/NADPH resulted in just a 14% decrease in cyt c peroxidase activity while incubation of cyt c ox with TXNL6 and TxrR/NADPH in the absence of MsrA resulted in 19% decrease in cyt c peroxidase activity. p values were obtained using Tukey's test following one-way ANOVA.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: Activity Assay, Incubation

    Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized cyt c (5 µg). Lane 1 untreated cyt c cleaved with CNBr. Lane 2 Oxidized cyt c (0.2 mM oxidized with 0.8 mM HOCl; a 4∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized cyt c (5 µg). Lane 1 untreated cyt c cleaved with CNBr. Lane 2 Oxidized cyt c (0.2 mM oxidized with 0.8 mM HOCl; a 4∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized cyt c (291 µM) treated with MsrA (1.9 µM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: Staining, SDS Page

    Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized α-crystallin (5 µg). Lane 1 untreated α-crystallin cleaved with CNBr. Lane 2 Oxidized α-crystallin (9.09 µM oxidized with 909 µm HOCl; a 100∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. Lane 5 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (20 µg; 2.78 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.

    Journal: PLoS ONE

    Article Title: TXNL6 Is a Novel Oxidative Stress-Induced Reducing System for Methionine Sulfoxide Reductase A Repair of α-Crystallin and Cytochrome C in the Eye Lens

    doi: 10.1371/journal.pone.0015421

    Figure Lengend Snippet: Coomassie staining of a Tricine-SDS-PAGE gel following CNBr cleavage of oxidized α-crystallin (5 µg). Lane 1 untreated α-crystallin cleaved with CNBr. Lane 2 Oxidized α-crystallin (9.09 µM oxidized with 909 µm HOCl; a 100∶1 Molar ratio) cleaved with CNBr. Lane 3 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and DTT (15 mM) for 2 h at 37°C and cleaved with CNBr. Lane 4 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (10 µg; 1.39 µM) for 2 h at 37°C and cleaved with CNBr. Lane 5 Oxidized α-crystallin (6.4 µM) treated with MsrA (100 nM) and TXNL6 (20 µg; 2.78 µM) for 2 h at 37°C and cleaved with CNBr. RA - reducing agent/system.

    Article Snippet: The resulting TXNL6 protein was examined by SDS-PAGE and western blot analysis using the ProteinTech rabbit polyclonal TXNL6-specific antibody for purity and identity.

    Techniques: Staining, SDS Page