Anti-N Cadherin antibody [EPR29626-10]
Anti-N Cadherin antibody [EPR29626-10]
- 20ul selling size
- Recombinant
- RabMAb
- KO Validated
- 了解详情
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Knockout Tested Rabbit Recombinant Monoclonal N Cadherin antibody. Suitable for I-ELISA, ICC/IF, WB and reacts with Recombinant fragment - Human, Human, Mouse samples.
查看别名
CD325, CDHN, NCAD, CDH2, Cadherin-2, CDw325, Neural cadherin, N-cadherin
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-N Cadherin antibody [EPR29626-10] (AB321897)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% Tween-20 permeabilized CDH2 KO HEK-293T (CDH2 knockout human embryonic kidney epithelial cell) ab255377 cells labelling N Cadherin with ab321897 at 1/50 (9.82 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing membranous staining in wildtype HEK-293T cells showing no staining in CDH2 knockout HEK-293T cells(shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-N Cadherin antibody [EPR29626-10] (AB321897)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% Tween-20 permeabilized A549 (human lung carcinoma epithelial cell) cells labelling N Cadherin with ab321897 at 1/50 (9.82 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing membranous and weak cytoplasmic staining in A549 cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue).
Negative control : MCF7(PMID : 9177902).
Image was taken with a confocal microscope (Leica-Microsystems TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-N Cadherin antibody [EPR29626-10] (AB321897)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% Tween-20 permeabilized C2C12 (mouse myoblast) cells labelling N Cadherin with ab321897 at 1/50 (9.82 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing membranous and weak cytoplasmic staining in C2C12 cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue).
Low expression : 4T1.
Image was taken with a confocal microscope (Leica-Microsystems TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- WB
Supplier Data
Western blot - Anti-N Cadherin antibody [EPR29626-10] (AB321897)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : MCF7 (PMID : 9177902).
Low expression : 4T1.
The molecular weight observed is consistent with what has been described in the literature (PMID : 22553038).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-N Cadherin antibody [EPR29626-10] (ab321897) at 1/1000 dilution
Lane 1:
293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 2:
MCF7 (human breast adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
C2C12 (mouse myoblast) whole cell lysate at 20 µg
Lane 4:
4T1 (mouse mammary gland carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 5:
A549 (human lung carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 6:
Human cerebellum tissue lysate at 20 µg
Lane 7:
Mouse cerebellum tissue lysate at 20 µg
Lane 8:
Mouse brain tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 80-130 kDa,36 kDa
false
Exposure time: 6s
- I-ELISA
Supplier Data
Indirect ELISA - Anti-N Cadherin antibody [EPR29626-10] (AB321897)
Indirect ELISA analysis of ab321897 at 1000-0 ng/ml. The Secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1 : 2500 dilution.
Antigen : Human Cadherin-2,Human Cadherin-4.
Antigen concentration : 1000 ng/ml
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补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
N-Cadherin significantly influences cell-cell interaction and communication facilitating cellular adhesion and signal transduction. It is a vital component of adherens junctions contributing to tissue morphogenesis and stability. N-Cadherin interacts with other cytoplasmic proteins such as catenins forming a complex essential for linking the actin cytoskeleton to the cell membrane. This interaction affects cellular behaviors including migration and differentiation.
Pathways
N-Cadherin plays a significant role in the neural development and epithelial-to-mesenchymal transition (EMT) pathways important for development and cancer progression. It engages with related proteins such as beta-catenin which helps transduce signals within these pathways. N-Cadherin's interactions within these pathways highlight its role in maintaining multicellular structure and signaling processes important for development and pathogenesis.
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