Anti-NCX1 antibody (ab151608)
Key features and details
- Rabbit polyclonal to NCX1
- Suitable for: WB, IHC-P
- Reacts with: Mouse, Rat
- Isotype: IgG
Overview
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Product name
Anti-NCX1 antibody
See all NCX1 primary antibodies -
Description
Rabbit polyclonal to NCX1 -
Host species
Rabbit -
Tested Applications & Species
See all applications and species dataApplication Species IHC-P MouseWB MouseRat -
Immunogen
Synthetic peptide corresponding to Mouse NCX1 aa 650-750 conjugated to keyhole limpet haemocyanin.
Database link: P70414 -
Positive control
- This antibody gave a positive signal in both Mouse and Rat Heart tissue lysate within WB. IHC-P (FFPE): Mouse Kidney (Normal)
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 or -80°C. Avoid freeze / thaw cycle. -
Storage buffer
pH: 7.40
Preservative: 0.02% Sodium azide
Constituent: PBS
Batches of this product that have a concentrationConcentration information loading...Purity
Immunogen affinity purifiedClonality
PolyclonalIsotype
IgGResearch areas
Associated products
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Compatible Secondaries
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Isotype control
Applications
The Abpromise guarantee
Our Abpromise guarantee covers the use of ab151608 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
GuaranteedTested applications are guaranteed to work and covered by our Abpromise guarantee.
PredictedPredicted to work for this combination of applications and species but not guaranteed.
IncompatibleDoes not work for this combination of applications and species.
Application Species IHC-P MouseWB MouseRatAll applications RabbitHorseApplication Abreviews Notes WB Use a concentration of 1 µg/ml. Detects a band of approximately 120 kDa (predicted molecular weight: 108 kDa).IHC-P Use a concentration of 1 µg/ml. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.Notes WB
Use a concentration of 1 µg/ml. Detects a band of approximately 120 kDa (predicted molecular weight: 108 kDa).IHC-P
Use a concentration of 1 µg/ml. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.Target
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Function
Rapidly transports Ca(2+) during excitation-contraction coupling. Ca(2+) is extruded from the cell during relaxation so as to prevent overloading of intracellular stores. -
Tissue specificity
Expressed in cardiac sarcolemma, brain, kidney, liver, pancreas, skeletal muscle, placenta and lung. -
Sequence similarities
Belongs to the sodium/potassium/calcium exchanger family. SLC8 subfamily.
Contains 2 Calx-beta domains. -
Cellular localization
Cell membrane. - Information by UniProt
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Database links
- Entrez Gene: 20541 Mouse
- Entrez Gene: 100328570 Rabbit
- Entrez Gene: 29715 Rat
- SwissProt: P70414 Mouse
- SwissProt: Q01728 Rat
- Unigene: 265834 Mouse
- Unigene: 118972 Rat
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Alternative names
- CNC antibody
- DKFZp779F0871 antibody
- MGC119581 antibody
see all
Images
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All lanes : Anti-NCX1 antibody (ab151608) at 1 µg/ml
Lane 1 : Heart (Mouse) Tissue Lysate (ab27255)
Lane 2 : Heart (Rat) Tissue Lysate (ab54976)
Lysates/proteins at 25 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/10000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 108 kDa
Observed band size: 120 kDa why is the actual band size different from the predicted?
Additional bands at: 30 kDa (possible non-specific binding), 68 kDa (possible non-specific binding)
Exposure time: 30 secondsThis blot was produced using a 10% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 5% Bovine Serum Albumin before being incubated with ab151608 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution.
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IHC image of ab151608 staining in Mouse Kidney formalin fixed paraffin embedded tissue section, performed on a Leica Bond system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab151608, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Protocols
Datasheets and documents
References (4)
ab151608 has been referenced in 4 publications.
- Neubert P et al. NCX1 represents an ionic Na+ sensing mechanism in macrophages. PLoS Biol 18:e3000722 (2020). PubMed: 32569301
- Hadipour-Lakmehsari S et al. Nanoscale reorganization of sarcoplasmic reticulum in pressure-overload cardiac hypertrophy visualized by dSTORM. Sci Rep 9:7867 (2019). PubMed: 31133706
- Bai T et al. Resveratrol protects against lipopolysaccharide-induced cardiac dysfunction by enhancing SERCA2a activity through promoting the phospholamban oligomerization. Am J Physiol Heart Circ Physiol 311:H1051-H1062 (2016). PubMed: 27591219
- Long Z et al. The reverse-mode NCX1 activity inhibitor KB-R7943 promotes prostate cancer cell death by activating the JNK pathway and blocking autophagic flux. Oncotarget 7:42059-42070 (2016). PubMed: 27275542
Images
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All lanes : Anti-NCX1 antibody (ab151608) at 1 µg/ml
Lane 1 : Heart (Mouse) Tissue Lysate (ab27255)
Lane 2 : Heart (Rat) Tissue Lysate (ab54976)
Lysates/proteins at 25 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/10000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 108 kDa
Observed band size: 120 kDa why is the actual band size different from the predicted?
Additional bands at: 30 kDa (possible non-specific binding), 68 kDa (possible non-specific binding)
Exposure time: 30 secondsThis blot was produced using a 10% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 5% Bovine Serum Albumin before being incubated with ab151608 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution.
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IHC image of ab151608 staining in Mouse Kidney formalin fixed paraffin embedded tissue section, performed on a Leica Bond system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab151608, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.