Anti-Lrp2 / Megalin antibody [EPR30413-507]
- RabMAb
- Recombinant
- 20ul selling size
- 각 태그의 뜻
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- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling Lrp2 / Megalin with ab324981 at 1/5000 (0.101 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat kidney (PMID : 7937880). The primary antibody was incubated for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling Lrp2 / Megalin with ab324981 at 1/5000 (0.101 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse kidney. The primary antibody was incubated for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- WB
Lab
Western blot - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : B16-F10, Neuro-2a
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) 1 : 10000 (124Kda).
All lanes:
Western blot - Anti-Lrp2 / Megalin antibody [EPR30413-507] (ab324981) at 1/1000 dilution
Lane 1:
F9 (mouse embryonal carcinoma epithelial cell) whole cell lysate at 40 µg
Lane 2:
B16-F10 (mouse skin melanoma cell) whole cell lysate at 40 µg
Lane 3:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 40 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 519 kDa,124 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : skeletal muscle, liver(PMID : 7937880)
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) 1 : 10000 (124Kda).
Exposure time : Lanes1-2 : 6 seconds, lanes3-6 : 15 seconds
All lanes:
Western blot - Anti-Lrp2 / Megalin antibody [EPR30413-507] (ab324981) at 1/1000 dilution
Lane 1:
Mouse kidney tissue lysate at 20 µg
Lane 2:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 3:
Mouse placenta tissue lysate at 20 µg
Lane 4:
Mouse liver tissue lysate at 20 µg
Lane 5:
Rat kidney tissue lysate at 20 µg
Lane 6:
Rat liver tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 519 kDa,124 kDa
false
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling Lrp2 / Megalin with ab324981 at 1/5000 (0.101 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on rat skeletal muscle (PMID : 7937880). The primary antibody was incubated for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Lrp2 / Megalin with ab324981 at 1/5000 (0.101 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse liver. The primary antibody was incubated for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling Lrp2 / Megalin with ab324981 at 1/5000 (0.101 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse skeletal muscle. The primary antibody was incubated for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Lrp2 / Megalin antibody [EPR30413-507] (AB324981)
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling Lrp2 / Megalin with ab324981 at 1/5000 (0.101 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on rat liver (PMID : 7937880). The primary antibody was incubated for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
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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.
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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