- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GluN2D antibody [EPR30355-38] (AB326329)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling GluN2D with ab326329 at 1/500 (1.012 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse cerebrum (PMID : 25164652; PMID : 10216082). The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GluN2D antibody [EPR30355-38] (AB326329)
Immunohistochemical analysis of paraffin-embedded Mouse spinal cord tissue labeling GluN2D with ab326329 at 1/500 (1.012 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse spinal cord. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Lab
Western blot - Anti-GluN2D antibody [EPR30355-38] (AB326329)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : colon, skeletal muscle, liver, spleen.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-GluN2D antibody [EPR30355-38] (ab326329) at 1/1000 dilution
Lane 1:
Mouse P5 brain tissue lysate at 20 µg
Lane 2:
Mouse colon tissue lysate at 20 µg
Lane 3:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 4:
Mouse liver tissue lysate at 20 µg
Lane 5:
Mouse spleen tissue lysate at 20 µg
Lane 6:
Mouse cerebellum 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 1/20000 dilution
Observed band size: 165 kDa,36 kDa
false
Exposure time: 125s
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GluN2D antibody [EPR30355-38] (AB326329)
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling GluN2D with ab326329 at 1/500 (1.012 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 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Lab
Western blot - Anti-GluN2D antibody [EPR30355-38] (AB326329)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with overexpressed human GluN2A, GluN2B or GluN2C by western blot.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
In Western blot, Anti-6X His tag® antibody [EPR20547] - ChIP Grade (ab213204) (1 : 5000) (165KDa).
All lanes:
Western blot - Anti-GluN2D antibody [EPR30355-38] (ab326329) at 1/1000 dilution
Lane 1:
293T (human embryonic kidney epithelial cell) cells transfected with an empty vector containing a myc-His-tag® whole cell lysate at 10 µg
Lane 2:
293T cells transfected with a human GluN2A expression vector containing a myc-His-tag® whole cell lysate at 10 µg
Lane 3:
293T cells transfected with a human GluN2B expression vector containing a myc-His-tag® whole cell lysate at 10 µg
Lane 4:
293T cells transfected with a human GluN2C expression vector containing a myc-His-tag® whole cell lysate at 10 µg
Lane 5:
293T cells transfected with a human GluN2D expression vector containing a myc-His-tag® whole cell lysate at 10 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 1/20000 dilution
Observed band size: 165 kDa,36 kDa
false
Exposure time: 125s
Reactivity 정보
제품 세부 정보
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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