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Discovery Antibodies/A23187/5 mg/A-600-5 mg
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Cat #: AGP-001 Alternative Name Voltage-dependent L-type calcium channel subunit α1CLyophilized Powder Lyophilized PowderThis product is freeze dried. All water molecules have been removed.Antigen Incl. Antigen Incl.This antibody is shipped with its antigen FREE of charge!Type: PolyclonalHost: Guinea pigReactivity: h, m, r Immunogen - + Peptide (C)TTKINMDDLQPSENEDKS, corresponding to amino acid residues 848-865 of rat CaV1.2 (Accession P22002). Intracellular loop between domains II and III.Accession (Uniprot) Number P22002Gene ID 24239Peptide confirmation Confirmed by amino acid analysis and mass spectrometry.Homology Mouse - identical; guinea pig - 17/18 amino acid residues identical; human, rabbit - 16/18 amino acid residues identical. RRID AB_11219156.Purity Affinity purified on immobilized antigen.Form Lyophilized powder. Reconstituted antibody contains phosphate buffered saline (PBS), pH 7.4, 1% BSA, 0.05% NaN3.Isotype Guinea pig total IgG.Storage before reconstitution The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C.Reconstitution 25 µl, 50 µl or 0.2 ml double distilled water (DDW), depending on the sample size.Antibody concentration after reconstitution 0.8 mg/ml.Storage after reconstitution The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods, small aliquots should be stored at -20°C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).Negative control antigen storage before reconstitution Lyophilized powder can be stored intact at room temperature for 2 weeks. For longer periods, it should be stored at -20°C.Negative control antigen reconstitution 100 µl double distilled water (DDW).Negative control antigen storage after reconstitution -20°C.Preadsorption Control 1 µg peptide per 1 µg antibody.Standard quality control of each lot Western blot analysis.Applications: if, ih, wbMay also work in: ic*, ifc*, ip* Western blot - + Western blot analysis of rat brain membrane:1. Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001), (1:200).2. Guinea pig Anti-CaV1.2 (CACNA1C) Antibody, preincubated with the negative control antigen.Western blot analysis of CaV1.2-transfected Xenopus oocytes (lane 1) and non-transfected oocytes lysates (lane 2):1. Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001), (1:200) in CaV1.2 (CACNA1C) Channel Overexpressed Membrane Fractions (LX-104).2. Guinea pig Anti-CaV1.2 (CACNA1C) Antibody in non-transfected oocytes. Immunohistochemistry - + Immuno-colocalization of CaV1.2 and GABA(A) α1 Receptor in rat cerebellumImmunohistochemical staining of rat cerebellum using Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001) and Anti-GABA(A) α1 Receptor (extracellular)-ATTO-488 Antibody (#AGA-001-AG). A. CaV1.2 (red) is detected mostly in Purkinje cells (arrow). B. In the same section, GABA(A) α1 Receptor (green) is observed in the granule layer. C. Merge of the two images suggests some colocalization between CaV1.2 and GABA(A) α1 Receptor in the rat granule layer but only CaV1.2 appears in Purkinje cells.Expression of CaV1.2 in human atriaImmunohistochemical staining of human left atrium using Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001), (1:100).The picture was kindly provided by Dr. Van Wagoner, D.R. from the Department of Molecular Cardiology, Cleveland Clinic, Cleveland, Ohio, USA. Lovano, B. and Peterson, J. collected the data.Expression of CaV1.2 in rat heartImmunohistochemical staining of rat heart paraffin embedded sections using Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001). A. CaV1.2 staining (green) appears mainly in the cardiac muscle, and in a lesser intensity in the tunica intima layer of the smooth muscle of the muscular arteries. B. Nuclear staining using DAPI as the counter stain. C. Merged images of A and B.Expression of CaV1.2 in mouse hippocampusImmunohistochemical staining of mouse dentate gyrus using Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001). A. CaV1.2 (green) appeared in the outer molecular layer of the dentate gyrus and in the granule layer. B. Counterstain with DAPI (blue) outlines the granule layer of the dentate gyrus. References1. Bauer, C.S. et al. (2010) Curr. Opin. Neurobiol. 20, 563.2. Arikkath, J. et al. (2003) Curr. Opin. Neurobiol. 13, 298.3. Catterall, W.A. (2000) Annu. Rev. Cell. Dev. Biol. 16, 521.4. Davies, A. et al. (2007) Trends Pharmacol. Sci. 28, 220.5. Dai, S. et al. (2009) Physiol. Rev. 89, 411.6. Zuccotti, A. et al. (2011) Trends Pharmacol. Sci. 32, 366.7. Hell, J.W. et al. (1996) Proc. Natl. Acad. Sci. U.S.A. 93, 3362.8. De Jongh, K.S. et al. (1996) Biochemistry 35, 10392.9. Gao, T. et al. (2001) J. Biol. Chem. 276, 21089.10. Liao, P. et al. (2010) Pflugers. Arch. 460, 353. Scientific background - + Voltage-gated Ca2+ channels (CaV), enable the passage of Ca2+ ions in a voltage dependent manner. These heteromeric entities are formed in part by the pore-forming α1 subunit which determines the biophysical and pharmacological properties of the channel1.L-type Ca2+ channels make up one of three voltage-gated Ca2+ channel families. Four different α1 isoforms (CaV1.1 to CaV1.4) belong to the L-type subfamily. Structurally, each α1 subunit has four homologous domains (I-IV) and each domain has a six transmembrane section. Like many other voltage-gated channels, L-type Ca2+ channels have auxiliary subunits which are responsible for modulating the surface expression and properties of the channels2-5.CaV1.1 is mostly expressed in the skeletal muscle, while CaV1.4 is mainly detected in the retina. The expression of both CaV1.2 and CaV1.3 is more extensive and includes neurons, heart, smooth muscle, inner ear, retina and pancreas6. L-type Ca2+ channels are involved in and modulate a variety of physiological functions such as muscle contraction, hormone secretion, neuronal excitability and gene expression5.CaV1.2 undergoes various post-translational modifications. For example, it can undergo proteolytic cleavage at its C-terminal. This cleavage has been shown to take place in neurons following the activation of NMDA receptors5,7 and in the heart5,8,9. The cleaved moiety can still interact with the channel and its general purpose is to modulate channel activity5. Other postranslation modifications of the channel include phosphorylation of CaV1.2 by a number of kinases such as PKA, PKC, Src and CaMKII5. In addition, it is not surprising that phosphatases also regulate channel activity, as they are required to antagonize the activity of the various kinases known to phosphorylate CaV1.2 5.The fact that CaV1.2 plays a prominent role in proper cardiac function has prompted endless studies regarding its regulation. Such studies have concluded that dysregulation of the channel leads to anomalies in heart contraction and thus heart failure5. Likewise, CaV1.2 defects have been detected in autism and bipolar disorder10.Application key: CBE- Cell-based ELISA, FC- Flow cytometry, ICC- Immunocytochemistry, IE- Indirect ELISA, IF- Immunofluorescence, IFC- Indirect flow cytometry, IHC- Immunohistochemistry, IP- Immunoprecipitation, LCI- Live cell imaging, N- Neutralization, WB- Western blotSpecies reactivity key: H- Human, M- Mouse, R- RatLyophilized PowderNegative Control Antigen IncludedClick here to receive a 25 µl free trial sample! Certificate of Analysis MSDSImage & Title: Immuno-colocalization of CaV1.2 and GABA(A) α1 Receptor in rat and mouse hippocampusImmunohistochemical staining of mouse and rat hippocampal dentate gyrus using Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001) and Anti-GABA(A) α1 Receptor (extracellular)-ATTO-488 Antibody (#AGA-001-AG) in the same section. Both CaV1.2 (red) and GABA(A) α1 Receptor (green) are detected in neuron-shaped cells (arrows). Staining suggests partial colocalization between CaV1.2 and GABA(A) α1 Receptor in a sub-population of dentate gyrus neurons. A. Mouse hippocampus. B. Rat hippocampus.Last update: 21/11/2019Guinea pig Anti-CaV1.2 (CACNA1C) Antibody (#AGP-001), raised in guinea pigs, is a highly specific antibody directed against an epitope of the rat protein. The antibody can be used in western blot and immunohistochemistry applications. It and has been designed to recognize CaV1.2 from mouse, rat and human samples. The antigen used to immunize guinea pigs is the same as Anti-CaV1.2 (CACNA1C) Antibody (#ACC-003) raised in rabbit. Our line of guinea pig antibodies enables more flexibility with our products such as immuno-colocalization studies, immunoprecipitation, etc.For research purposes only, not for human use

Discovery®抗体是剑桥生物化学研究所(CRB)的新目录抗体业务。



CRB是世界上第二大多肽公司,也是抗体研究市场的领跑者,从目录业务到现在已有22年的休息期(1994-2016年),现在是第37年(2017年),CRB推出了一个全新的现成抗体业务,名为Discovery®抗体。



Discovery®抗体将专注于研究抗体(早期药物“Discovery”),并将补充我们非常成功和长期的定制抗体业务(www.crbdiscovery.com网站). 我们以新颖、复杂、稀有和翻译后修饰的特异性抗体而闻名,这些备受追捧的目标将出现在我们的发现®抗体目录范围内。



我们于2017年2月推出了我们的发现®抗体,一年后发现®肽,大约240年后,詹姆斯·库克船长(他那个时代最伟大的探险家)于1776年从英国乘“发现”号船出发,包租全球的新水域和“发现”新大陆。因此,“发现”这个名字似乎适合东北部的一家制造商——詹姆斯·库克的家乡。



在17世纪末对世界各地新发现的土地的探索和2000年医学研究的新“发现”以及人类基因组的绘制之间产生了进一步的相似之处。



有关更多详情,请参阅我们发布的Discovery®抗体的新闻稿



剑桥研究生物化学(www.crbdiscovery.com网站)是一家领先的定制肽和抗体工具的独立生产商,为全球制药、生命科学和学术领域的研究人员提供服务。其产品的主要用途是作为定制的实验室级试剂,用于证明早期药物发现中的主要研究,并支持临床研究中的生物标记物方案。该公司生产各种口味的肽,从简单到改性,稳定,从毫克到克标到最高纯度的染料标签。

Discovery®抗体是剑桥生物化学研究所(CRB)的新抗体目录业务

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