Anti-Pan Cav2 antibody [EPR28073-84]
- BOND RX™ Validated
- 20ul selling size
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal CACNA1A antibody. Suitable for WB, IHC-P, IHC-Fr and reacts with Mouse, Rat, Transfected cell lysate - Mouse samples.
View Alternative Names
Caca1a, Cach4, Cacn3, Cacnl1a4, Ccha1a, Cacna1a, Voltage-dependent P/Q-type calcium channel subunit alpha-1A, Brain calcium channel I, Voltage-gated calcium channel subunit alpha Cav2.1, BI
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling Pan Cav2 with ab315092 at 1/100 (5.16 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on rat liver. The section was incubated with ab315092 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
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Pan Cav2 with ab315092 at 1/100 (5.16 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse liver. The section was incubated with ab315092 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-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse liver (fresh) tissue labeling Pan Cav2 with ab315092 at 1/50 (10.32 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Negative control : confocal image showing no staining on mouse liver. The section was incubated with ab315092 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat liver (fresh) tissue labeling Pan Cav2 with ab315092 at 1/50 (10.32 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Negative control : confocal image showing no staining on rat liver. The section was incubated with ab315092 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling Pan Cav2 with ab315092 at 1/100 (5.16 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse cerebrum. The section was incubated with ab315092 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
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling Pan Cav2 with ab315092 at 1/100 (5.16 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat cerebrum. The section was incubated with ab315092 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
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of paraffin-embedded Mouse cerebellum tissue labeling Pan Cav2 with ab315092 at 1/100 (5.16 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse cerebellum. The section was incubated with ab315092 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-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebellum (fresh) tissue labeling Pan Cav2 with ab315092 at 1/50 (10.32 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Confocal image showing positive staining on mouse cerebellum. The section was incubated with ab315092 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebellum (fresh) tissue labeling Pan Cav2 with ab315092 at 1/50 (10.32 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Confocal image showing positive staining on rat cerebellum. The section was incubated with ab315092 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.
- WB
Supplier Data
Western blot - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : liver, testis(PMID : 8929530)
Lysates were freshly made and used for Western blotting immediately to minimize protein degradation.
Samples are non-boiled as boiling may cause protein aggregation.
The identity of the lower MW band at approximately 100 kDa may represent an N-terminal truncated isoform of CACNA1A (PMID : 7673157).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Pan Cav2 antibody [EPR28073-84] (ab315092) at 1/1000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Mouse liver tissue lysate at 20 µg
Lane 3:
Mouse testis tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 100 kDa,267 kDa,36 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : spleen, liver(PMID : 8929530)
Samples are non-boiled as boiling may cause protein aggregation.
The identity of the lower MW band at approximately 100 kDa may represent an N-terminal truncated isoform of CACNA1A (PMID : 7673157).
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-Pan Cav2 antibody [EPR28073-84] (ab315092) at 1/1000 dilution
Lane 1:
Rat brain tissue lysate at 20 µg
Lane 2:
Rat spleen tissue lysate at 20 µg
Lane 3:
Rat liver tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 100 kDa,267 kDa,124 kDa
false
Exposure time: 103s
- WB
Supplier Data
Western blot - Anti-Pan Cav2 antibody [EPR28073-84] (AB315092)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody reacts with CAV2.2 and CAV2.3.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-6X His tag® antibody [EPR20547] - ChIP Grade (ab213204) staining at 1/5000 dilution.
All lanes:
Western blot - Anti-Pan Cav2 antibody [EPR28073-84] (ab315092) at 1/1000 dilution
Lane 1:
293T cells transfected with an empty vector containing a His-tag, whole cell lysate at 10 µg
Lane 2:
293T cells transfected with a mouse CAV2.1 expression vector containing a His-tag, whole cell lysate at 10 µg
Lane 3:
293T cells transfected with a mouse CAV2.2 expression vector containing a His-tag, whole cell lysate at 10 µg
Lane 4:
293T cells transfected with a mouse CAV2.3 expression vector containing a His-tag, whole cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 100 kDa,110 kDa,120 kDa
false
Exposure time: 10s
Related conjugates and formulations (1)
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Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Cav2 channels play key roles in neurotransmitter release muscle contraction and hormone secretion. These channels form part of multiprotein complexes that involve various auxiliary subunits which modulate their function and localization. Through their regulation of calcium influx Cav2 channels critically impact synaptic transmission and plasticity in neuronal communication. They also contribute to excitation-contraction coupling in muscle cells enabling the precise control of muscle actions.
Pathways
Cav2 channels heavily influence calcium signaling pathways and synaptic plasticity pathways. Within the calcium signaling pathway their activity directly alters intracellular calcium concentrations which modulate downstream signaling cascades. These channels closely interact with proteins such as SNARE proteins and synaptotagmin in neurotransmitter release. In pathways related to synaptic plasticity Cav2 channels influence long-term potentiation impacting learning and memory processes.
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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