Anti-GST抗体[3G10/1B3]
Anti-GST antibody [3G10/1B3]
- Lab Essentials
- 了解详情
5
(3 Reviews)
|
(42 Publications)
Mouse Monoclonal GST antibody. Carrier free. Suitable for IP, WB and reacts with Tag samples. Cited in 42 publications. Immunogen corresponding to Recombinant Full Length Protein corresponding to Schistosoma japonicum Glutathione S-transferase class-mu 26 kDa isozyme.
查看别名
Glutathione S-transferase class-mu 26 kDa isozyme, GST 26, Sj26 antigen, SjGST
- WB
Lab
Western blot - Anti-GST antibody [3G10/1B3] (AB92)
Western blot : Anti-FOXA2 antibody [EPR22919-71] - ChIP Grade ab256493 staining at 1/1000 dilution, shown in green; anti-GST antibody [3G10/1B3] ab92 staining at 1 g/mL, shown in magenta. A band was observed at 78 kDa. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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-Rabbit 800CW and Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-FOXA2 antibody [EPR22919-71] - ChIP Grade (<a href='/products/primary-antibodies/foxa2-antibody-epr22919-71-chip-grade-ab256493'>ab256493</a>) at 1/1000 dilution
Lane 1:
FOXA1 Recombinant Protein (GST Tag) at 0.1 µg
Lane 2:
FOXA2 Recombinant Protein (GST Tag) at 0.1 µg
Lane 3:
FOXA3 Recombinant Protein (GST Tag) at 0.1 µg
Secondary
All lanes:
Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 78 kDa
Observed band size: 78 kDa
false
- WB
Lab
Western blot - Anti-GST antibody [3G10/1B3] (AB92)
Western blot : Anti-FOXA2 antibody [EPR4466] ab108422 staining at 1/1000 dilution, shown in green; [LOADING CONTROL] loading control staining at 1/[DILUTION] dilution, shown in magenta. A band was observed at 78 kDa. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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-Rabbit 800CW and Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-FOXA2 antibody [EPR4466] (<a href='/products/primary-antibodies/foxa2-antibody-epr4466-ab108422'>ab108422</a>) at 1/1000 dilution
Lane 1:
FOXA1 Recombinant Protein (GST Tag) at 0.1 µg
Lane 2:
FOXA2 Recombinant Protein (GST Tag) at 0.1 µg
Lane 3:
FOXA3 Recombinant Protein (GST Tag) at 0.1 µg
Secondary
All lanes:
Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 78 kDa
Observed band size: 78 kDa
false
- WB
Lab
Western blot - Anti-GST antibody [3G10/1B3] (AB92)
Western blot : Anti-FOXA1 antibody ab23738 staining at 0.7 µg/mL, shown in green; Mouse anti GST ab92 loading control staining at 1/1000 dilution, shown in magenta. A band was observed at 76 kDa. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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-Rabbit 800CW and Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-FOXA1 + FOXA2 antibody (<a href='/products/primary-antibodies/foxa1-antibody-ab23738'>ab23738</a>) at 0.7 µg/mL
Lane 1:
FOXA1 Recombinant Protein at 0.1 µg
Lane 2:
FOXA2 Recombinant Protein at 0.1 µg
Lane 3:
FOXA3 Recombinant Protein at 0.1 µg
Secondary
All lanes:
Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 52 kDa
Observed band size: 76 kDa
false
- WB
Lab
Western blot - Anti-GST antibody [3G10/1B3] (AB92)
Anti-FOXA1 + FOXA2 + FOXA3 antibody [RM1119] ab317046 staining at 1/1000 dilution, shown in green; Mouse anti GST (ab92) loading control staining at 1/200 dilution, shown in magenta. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-FOXA1 + FOXA2 + FOXA3 antibody [RM1119] (<a href='/products/primary-antibodies/foxa1-antibody-rm1119-ab317046'>ab317046</a>) at 1/1000 dilution
Lane 1:
FOXA1 Recombinant Protein (GST Tag) at 0.1 µg
Lane 2:
FOXA2 Recombinant Protein (GST Tag) at 0.1 µg
Lane 3:
FOXA3 Recombinant Protein (GST Tag) at 0.1 µg
Secondary
All lanes:
Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 52 kDa,50 kDa,37 kDa
Observed band size: 78 kDa,76 kDa,63 kDa
false
反应性数据
产品详情
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
GST enzymes participate in critical cellular detoxification processes enhancing the solubility of toxins. As part of these processes GST enzymes do not function as part of a larger complex but are individual actors within the cell. They facilitate the conjugation reactions fundamental to cellular metabolism and detoxification making them essential for maintaining cellular health.
Pathways
GST enzymes contribute significantly to the metabolic breakdown pathways like the xenobiotic metabolism pathway. This pathway involves proteins such as cytochrome P450 enzymes which often function upstream to modify compounds for further GST action. GSTs are important for efficiently detoxifying potentially harmful substances preventing cellular damage.
产品实验方案
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靶点信息
文献 (42)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 16:5892 PubMed40603292
2025
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The New phytologist 245:2726-2743 PubMed39887382
2025
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Nature communications 15:9689 PubMed39516491
2024
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The Journal of cell biology 223: PubMed39514288
2024
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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11:e2405459 PubMed39206796
2024
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Frontiers in immunology 15:1379175 PubMed39086481
2024
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Cell genomics 4:100550 PubMed38697125
2024
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Nature communications 14:7838 PubMed38030598
2023
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Plant communications 5:100673 PubMed37596786
2023
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Insect science 30:1607-1621 PubMed36915030
2023
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