Anti-MARVELD2/Tricellulin antibody [54H19L38] (ab203567)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [54H19L38] to MARVELD2/Tricellulin
- Suitable for: WB, ICC/IF, IP
- Reacts with: Dog, Human
Overview
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Product name
Anti-MARVELD2/Tricellulin antibody [54H19L38]
See all MARVELD2/Tricellulin primary antibodies -
Description
Rabbit monoclonal [54H19L38] to MARVELD2/Tricellulin -
Host species
Rabbit -
Tested Applications & Species
See all applications and species dataApplication Species ICC/IF HumanIP HumanWB Human -
Immunogen
Recombinant fragment corresponding to Human MARVELD2/Tricellulin aa 350 to the C-terminus.
Database link: Q8N4S9 -
Positive control
- ICC/IF: Caco 2 cells; WB: Caco 2, HeLa, PANC1, MCF-7 and MDCK cell lysates IP: HeLa cells
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General notes
This product was previously labelled as MARVELD2
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. -
Storage buffer
Preservative: 0.09% Sodium azide
Constituent: 99% PBS -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
54H19L38 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-MARVELD2/Tricellulin antibody [54H19L38] (ab203567) at 2 µg
Lane 1 : Untransfected HeLa cells
Lane 2 : HeLa cells transfected with scrambled SiRNA
Lane 3 : HeLa cells transfected with MARVELD2/Tricellulin siRNA.
Secondary
All lanes : Goat anti-Rabbit IgG (H+L) secondary antibody at 1/40000 dilution
Predicted band size: 64 kDa
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All lanes : Anti-MARVELD2/Tricellulin antibody [54H19L38] (ab203567) at 1 µg/ml
Lane 1 : HeLa cell lysate
Lane 2 : PANC1 cell lysate
Lane 3 : MCF-7 cell lysate
Lysates/proteins at 30 µg per lane.
Secondary
All lanes : Goat anti-rabbit HRP conjugated at 1/2500 dilution
Predicted band size: 64 kDa
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Tricellulin was immunoprecipitated using 5 µg of ab203567 from lysate of HeLa (Lane 3). Normal Rabbit IgG was used as a Isotype control (Lane 2). 10 % input represents the cell extract used for immunoprecipitation (Lane 1). Western blot analysis was performed using ab203567 and Goat anti-Rabbit IgG (H+L) Secondary Antibody, HRP conjugate at 1:2500 dilution. Chemiluminescent detection was performed using ECL Western Blotting Substrate.
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Immunofluorescence analysis of Tricellulin was done on 90% confluent log phase Caco-2 cells. The cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilized with 0.25% Triton™ X-100 for 10 minutes, and blocked with 5% BSA for 1 hour at room temperature. The cells were labeled with ab203567 at 1 µg/mL in 1% BSA and incubated for 3 hours at room temperature and then labeled with Goat anti-Rabbit IgG (H+L) Secondary Antibody, Alexa Fluor® 488 conjugate at a dilution of 1/2000 for 45 minutes at room temperature (Panel a: green). Nuclei (Panel b: blue) were stained with DAPI. F-actin (Panel c: red) was stained with Alexa Fluor® 555 Rhodamine Phalloidin at 1/300. Panel d is a merged image showing cell junctional localization. Panel e is a no primary antibody control. The images were captured at 60X magnification.
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Immunofluorescent analysis of Caco 2 cells labeling MARVELD2/Tricellulin using ab203567 at 8 μg/mL. Alexa Fluor® 488 goat anti-rabbit at 1/1000 was used as secondary antibody (green). DAPI staining of nucleus (top left, blue), cell-cell junctions were labeled using a anti- Occludin antibody (top right, red). Bottom right: merged image.
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All lanes : Anti-MARVELD2/Tricellulin antibody [54H19L38] (ab203567) at 3 µg/ml
Lane 1 : Caco 2 cell lysate
Lane 2 : MDCK cell lysate
Predicted band size: 64 kDa
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