Anti-IRS2 抗体 [EPR904(2)]
Anti-IRS2 antibody [EPR904(2)]
- RabMAb
- Recombinant
- KO Validated
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(30 Publications)
Rabbit Recombinant Monoclonal IRS2 antibody. Suitable for IHC-P, WB, ICC/IF, Flow Cyt (Intra) and reacts with Rat, Human, Mouse samples. Cited in 30 publications.
別名を表示する
Insulin receptor substrate 2, IRS-2, IRS2
- WB
Lab
Western blot - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Blocking/Diluting buffer and concentration : 5% NFDM/TBST.
Exposure time :
Left image : 180 seconds
Right image : 40 seconds
Although some papers support the expression in liver (PMID : 30202052), A549 (PMID : 30988063), NCI-H1299 (PMID : 30988063), LADMAC (PMID : 29115630), MDA-MB-231 (PMID : 29685905) and MEF (PMID : 30679431), ab134101 can't detect the target band in these samples, even at the dilution of 1 : 200.
All lanes:
Western blot - Anti-IRS2 antibody [EPR904(2)] (ab134101) at 1/1000 dilution
Lane 1:
Rat liver lysates at 20 µg
Lane 2:
Human liver lysates at 20 µg
Lane 3:
A375 (human malignant melanoma epithelial cell) whole cell lysates at 20 µg
Lane 4:
A549 (human lung carcinoma epithelial cell) whole cell lysates at 20 µg
Lane 5:
NCI-H1299 (human lung carcinoma epithelial cell) whole cell lysates at 20 µg
Lane 6:
LADMAC (Mouse bone marrow monocyte macrophage) whole cell lysates at 20 µg
Lane 7:
MDA-MB-231 (human breast adenocarcinoma epithelial cell) whole cell lysates at 20 µg
Lane 8:
MEF (Mouse embryonic fibroblast) whole cell lysates at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 137 kDa
Observed band size: 170-185 kDa
true
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Immunocytochemistry/Immunofluorescence analysis of SH-SY5Y cells labelling IRS2 with purified ab134101 at 1/300. Cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/1000) was used as the secondary antibody. DAPI (blue) was used as the nuclear counterstain. ab7291, a mouse anti-tubulin (1/1000) and ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/1000) were also used.
Control 1 : primary antibody (1/300) and secondary antibody, ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/1000).
Control 2 : ab7291 (1/1000) and secondary antibody, ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/1000).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Intracellular Flow Cytometry analysis of HeLa cells labelling IRS2 with purified ab134101 at 1/120 (red). Cells were fixed with 2% paraformaldehyde. A FITC-conjugated goat anti-rabbit IgG (1/500) was used as the secondary antibody. Black - Isotype control, rabbit monoclonal IgG. Blue - Unlabelled control, cells without incubation with primary and secondary antibodies.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human muscle tissue labelling IRS2 with unpurified ab134101 at a dilution of 1/50.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-IRS2 antibody [EPR904(2)] (AB134101)
ab134101 staining IRS2 in wild-type HEK293 cells (top panel) and IRS2 knockout HEK293 cells (bottom panel). The cells were fixed with 4% paraformaldehyde (10 min) permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated with ab134101 at 1/500 and ab7291 (Mouse monoclonal to alpha Tubulin) at 1/1000 dilution overnight at +4°C, followed by a further incubation at room temperature for 1h with a goat secondary antibody to rabbit IgG (Alexa Fluor® 488) (ab150081) at 2 μg/ml (shown in green) and a goat secondary antibody to mouse IgG (Alexa Fluor® 594) (ab150120) at 2 μg/ml (shown in red). Nuclear DNA was labelled in blue with DAPI.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast tissue labelling IRS2 with unpurified ab134101 at a dilution of 1/50.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of rat kidney tissue labelling IRS2 with purified ab134101 at 1/500. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. ab97051, a HRP-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/500). Negative control using PBS instead of primary antibody. Counterstained with hematoxylin.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Overlay histogram showing HeLa cells stained with unpurified ab134101 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (unpurified ab134101, 1/1000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1μg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human kidney tissue labelling IRS2 with purified ab134101 at 1/500. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. ab97051, a HRP-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/500). Negative control using PBS instead of primary antibody. Counterstained with hematoxylin.
- WB
Lab
Western blot - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Lanes 1 - 4 : Merged signal (red and green). Green - ab134101 observed at 160 kDa. Red - loading control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) observed at 55kDa.
ab134101 was shown to react with IRS2 in wild-type HEK-293 cells in western blot with loss of signal observed in IRS2 knockout sample. Wild-type and IRS2 knockout HEK-293 cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1% Tween®) before incubation with ab134101 and ab7291 (Mouse anti-Alpha Tubulin [DM1A]) overnight at 4°C at a 1 in 1000 Dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-IRS2 antibody [EPR904(2)] (ab134101) at 1/1000 dilution
Lane 1:
Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
IRS2 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
Western blot - Human IRS2 knockout HEK-293 cell line (<a href='/products/cell-lines/human-irs2-knockout-hek-293-cell-line-ab264013'>ab264013</a>)
Lane 3:
A-375 cell lysate at 20 µg
Lane 4:
A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Predicted band size: 137 kDa,25 kDa
Observed band size: 160 kDa
false
- WB
Lab
Western blot - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-IRS2 antibody [EPR904(2)] (ab134101) at 1/5000 dilution
All lanes:
NIH/3T3 whole cell lysate - treated with insulin at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 137 kDa
Observed band size: 170-185 kDa
false
- WB
Lab
Western blot - Anti-IRS2 antibody [EPR904(2)] (AB134101)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-IRS2 antibody [EPR904(2)] (ab134101) at 20 µg
Lane 1:
HEK293 whole cell lysate - untreated at 20 µg
Lane 2:
HEK293 whole cell lysate - treated with insulin at 20 µg
Lane 3:
SH-SY5Y whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 137 kDa
Observed band size: 170-185 kDa
false
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APC Anti-IRS2 antibody [EPR904(2)]
Reactivity data
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補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
IRS2 acts in signal transduction and is a part of the insulin and insulin-like growth factor signaling pathways. IRS2 does not function alone but interacts with other molecules to propagate signals that regulate cellular processes. It is essential for glucose homeostasis and lipid metabolism playing a critical role in maintaining energy balance within the organism. IRS2 also mediates other biological processes like cell growth and differentiation.
Pathways
With regards to pathways IRS2 is involved in the insulin signaling and mTOR pathways. It serves as an important junction between metabolic and growth-promoting signals. Activation of IRS2 through insulin receptors leads to downstream signaling involving PI3K and Akt essential for mediating metabolic actions of insulin. It also interacts with mTOR a central protein in cell growth regulation. These pathways illustrate the integration of IRS2 in broader cellular responses to growth signals and energy availability.
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ターゲットの情報
文献 (30)
Recent publications for all applications. Explore the full list and refine your search
Journal of pineal research 75:e12897 PubMed37391878
2023
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Liver international : official journal of the International Association for the Study of the Liver 43:2560-2570 PubMed37337778
2023
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Cancers 15: PubMed36900240
2023
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Clinical and experimental pharmacology & physiology 49:1307-1318 PubMed35986631
2022
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PloS one 17:e0270830 PubMed35816477
2022
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International journal of environmental research and public health 18: PubMed34948750
2021
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Chinese medicine 16:128 PubMed34857022
2021
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Metabolism: clinical and experimental 127:154936 PubMed34801581
2021
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Molecular and cellular biology 42:e0032721 PubMed34694913
2021
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Cell & bioscience 11:141 PubMed34294142
2021
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