Anti-N Cadherin antibody [32/N-Cadherin] - BSA and Azide free
- KO Validated
- Recombinant
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Mouse Recombinant Monoclonal N Cadherin antibody. Carrier free. Suitable for IP, WB and reacts with Human, Rat, Mouse samples.
View Alternative Names
CD325, CDHN, NCAD, CDH2, Cadherin-2, CDw325, Neural cadherin, N-cadherin
- IP
Supplier Data
Immunoprecipitation - Anti-N Cadherin antibody [32/N-Cadherin] - BSA and Azide free (AB280380)
This data was developed using ab280375 the same antibody clone in a different buffer formulation.
N Cadherin was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate with ab280375 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab280375 at 1/1000 dilution. HRP-conjuagted mouse IgG for IP (ab131368) was used at 1/1000 dilution.
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10ug
Lane 2 : ab280375 IP in HeLa whole cell lysate
Lane 3 : Mouse monoclonal IgG1 (ab18443) instead of ab280375 in HeLa whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 23 seconds
The molecular weight observed is consistent with what has been described in the literature (PMID : 22553038)
All lanes:
Immunoprecipitation - Anti-N Cadherin antibody [32/N-Cadherin] (<a href='/en-us/products/primary-antibodies/n-cadherin-antibody-32-n-cadherin-ab280375'>ab280375</a>)
Predicted band size: 99 kDa
false
- WB
Supplier Data
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] - BSA and Azide free (AB280380)
This data was developed using ab280375, the same antibody clone in a different buffer formulation.
Blocking and Diluting buffer and concentration : 5% NFDM/TBST
Exposure time 15 seconds
Lanes 1-2 used the fresh lysates to minimize protein degradation.
All lanes:
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] (<a href='/en-us/products/primary-antibodies/n-cadherin-antibody-32-n-cadherin-ab280375'>ab280375</a>) at 1/5000 dilution
Lane 1:
HepG2 (human hepatocellular carcinoma epithelial cell), whole cell lysate at 10 µg
Lane 2:
293T (human embryonic kidney epithelial cell), whole cell lysate at 10 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Predicted band size: 99 kDa
Observed band size: 140 kDa
false
- WB
Supplier Data
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] - BSA and Azide free (AB280380)
This data was developed using ab280375, the same antibody clone in a different buffer formulation.
Blocking and Diluting buffer and concentration : 5% NFDM/TBST
Exposure time 26 seconds
Negative control : MCF7 (PMID : 9177902)
All lanes:
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] (<a href='/en-us/products/primary-antibodies/n-cadherin-antibody-32-n-cadherin-ab280375'>ab280375</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 10 µg
Lane 2:
MCF7 (human breast adenocarcinoma epithelial cell), whole cell lysate at 10 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Predicted band size: 99 kDa
Observed band size: 140 kDa
false
- WB
Supplier Data
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] - BSA and Azide free (AB280380)
This data was developed using ab280375, the same antibody clone in a different buffer formulation.
Blocking and Diluting buffer and concentration : Intercept® (TBS) Blocking Buffer diluted with an equal volume of 0.1% TBS.
Lanes 1 - 2 : Merged signal (red and green). Green - ab280375 observed at 130 kDa. Red - loading control ab181602 (Rabbit monoclonal [EPR16891] to GAPDH) observed at 36 kDa.
Lanes 1-2 : ab280375 Anti-CDH2 antibody was shown to react with CDH2 in 293T cells in Western blot. Loss of signal was observed when CDH2 knockout sample was used. Wild-type and CDH2 knockout samples were subjected to SDS-PAGE.
ab280375 and Anti-GAPDH antibody [EPR16891] (ab181602) were incubated at 4℃ overnight at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 680CW) (ab216777) and Goat anti-Mouse IgG H&L (IRDye® 800RD) (ab216772) secondary antibodies at 1/10000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] (<a href='/en-us/products/primary-antibodies/n-cadherin-antibody-32-n-cadherin-ab280375'>ab280375</a>) at 1/1000 dilution
Lane 1:
Wild-type 293T (human embryonic kidney epithelial cell), whole cell lysate at 20 µg
Lane 2:
CDH2 knockout 293T (human embryonic kidney epithelial cell), whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Mouse IgG H&L (IRDye® 800CW) (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-800cw-preadsorbed-ab216772'>ab216772</a>) and Goat Anti-Rabbit IgG H&L (IRDye® 680RD) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-680rd-preadsorbed-ab216777'>ab216777</a>) at 1/10000 dilution
Predicted band size: 99 kDa
Observed band size: 140 kDa
false
- WB
Supplier Data
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] - BSA and Azide free (AB280380)
This data was developed using ab280375, the same antibody clone in a different buffer formulation.
Blocking and Diluting buffer and concentration : 5% NFDM/TBST
Exposure time Lanes 1-2 : 15 seconds
Lanes 3 : 10 seconds
Lanes 4-5 : 26 seconds
All lanes:
Western blot - Anti-N Cadherin antibody [32/N-Cadherin] (<a href='/en-us/products/primary-antibodies/n-cadherin-antibody-32-n-cadherin-ab280375'>ab280375</a>) at 1/1000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Mouse kidney lysate at 10 µg
Lane 3:
Rat heart lysate at 10 µg
Lane 4:
C6 (rat glial tumor glial cell), whole cell lysate at 10 µg
Lane 5:
PC-12 (rat adrenal gland pheochromocytoma), whole cell lysate at 10 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Predicted band size: 99 kDa
Observed band size: 140 kDa
false
Related conjugates and formulations (1)
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Anti-N Cadherin antibody [32/N-Cadherin]
Reactivity data
Product details
ab280380 is the carrier-free version of ab280375.
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
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.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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