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AB315093

重组Anti-Pan Cav2抗体[EPR28073-84] - BSA and Azide free

Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free

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Rabbit Recombinant Monoclonal CACNA1A antibody. Carrier free. Suitable for WB, IHC-P, IHC-Fr and reacts with Mouse, Rat, Transfected cell lysate - Mouse samples.

查看别名

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

12 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-Fr

Supplier Data

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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.

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-Fr

Supplier Data

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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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.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-Fr

Supplier Data

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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.

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • IHC-Fr

Supplier Data

Immunohistochemistry (Frozen sections) - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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.

Western blot - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • WB

Supplier Data

Western blot - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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] (<a href='/products/primary-antibodies/pan-cav2-antibody-epr28073-84-ab315092'>ab315092</a>) 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='/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

Western blot - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • WB

Supplier Data

Western blot - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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] (<a href='/products/primary-antibodies/pan-cav2-antibody-epr28073-84-ab315092'>ab315092</a>) 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='/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

Western blot - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)
  • WB

Supplier Data

Western blot - Anti-Pan Cav2 antibody [EPR28073-84] - BSA and Azide free (AB315093)

This data was developed using ab315092, the same antibody clone in a different buffer formulation.

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] (<a href='/products/primary-antibodies/pan-cav2-antibody-epr28073-84-ab315092'>ab315092</a>) 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='/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

不同偶联物与剂型 (1)

关键信息

宿主种属

Rabbit

克隆

Monoclonal

克隆号

EPR28073-84

亚型

IgG

不含载体蛋白

Yes

反应种属

Mouse, Rat

应用

IHC-Fr, WB, IHC-P

applications

免疫原

The exact immunogen used to generate this antibody is proprietary information.

反应性数据

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产品详情

ab315093 is the carrier-free version of ab315092.

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.

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.

性能和储存信息

形式
Liquid
纯化工艺
Affinity purification Protein A
存储溶液
pH: 7.2 - 7.4 Constituents: PBS
运输条件
Blue Ice
推荐的短期储存条件
+4°C
推荐的长期储存条件
+4°C

补充信息

This supplementary information is collated from multiple sources and compiled automatically.

Pan Cav2 also known as Cav2 channels or voltage-gated calcium channels of the Cav2 family function mechanically to facilitate the influx of calcium ions through cellular membranes in response to membrane depolarization. These channels are important for converting electrical signals into calcium signals which play a big role in various cellular processes. Cav2 channels typically compose of the α1 subunit and several auxiliary subunits. The α1 subunit has an approximate mass of 190-250 kDa. Cav2 channels express widely throughout the nervous system including in neurons of the brain and spinal cord and also in cardiac and skeletal muscle cells.
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.

Cav2 channel dysfunction associates with neurological disorders such as migraine and epilepsy. Aberrant expression or mutation of Cav2 channel components disrupts normal neural excitation leading to these disorders. The channels also connect with auxiliary proteins such as α2δ subunits that can alter pain pathways implicating them in certain pain disorders. Moreover irregularities in Cav2 channel function may link to cardiac arrhythmias through interactions with cardiac proteins responsible for proper heartbeat rhythm.

产品实验方案

For this product, it's our understanding that no specific protocols are required. You can visit:

靶点信息

Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. The isoform alpha-1A gives rise to P and/or Q-type calcium currents. P/Q-type calcium channels belong to the 'high-voltage activated' (HVA) group and are specifically blocked by the spider omega-agatoxin-IVA (AC P54282) (By similarity). They are however insensitive to dihydropyridines (DHP).
See full target information Cacna1a

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