產(chǎn)品編號 | bs-2806R-Bio |
英文名稱 | Rabbit Anti-DHPR alpha 1/Biotin Conjugated antibody |
中文名稱 | 生物素標記的L-型電壓依賴型鈣通道α抗體 |
別 名 | alpha-1 polypeptide; cardiac muscle; isoform 1; L type; CAC1C_HUMAN; CACH 2; DHPR alpha 1; VDCC-L alpha; CACH2; CACN 2; CACN2; CACNA1C; CACNL1A1; Calcium channel; Calcium channel cardic dihydropyridine sensitive alpha 1 subunit; Calcium channel L type alpha 1 polypeptide isoform 1 cardiac muscle; Calcium channel voltage dependent L type alpha 1C subunit; CaV1.2; CCHL1A1; DHPR alpha 1 subunit; LQT8; TS; Voltage dependent L type calcium channel alpha 1C subunit; Voltage dependent L type calcium channel subunit alpha 1C; Voltage gated calcium channel alpha subunit Cav1.2; Voltage gated calcium channel subunit alpha Cav1.2; Voltage gated L type calcium channel Cav1.2 alpha 1 subunit, splice variant 10*; Voltage-dependent L-type calcium channel subunit alpha-1C; Voltage-gated calcium channel subunit alpha Cav1.2. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領(lǐng)域 | 心血管 免疫學(xué) 神經(jīng)生物學(xué) 通道蛋白 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, ) |
產(chǎn)品應(yīng)用 | ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 IF=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 249kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human DHPR alpha 1 |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
儲 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存條件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
產(chǎn)品介紹 |
background: This gene encodes an alpha-1 subunit of a voltage-dependent calcium channel. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. The alpha-1 subunit consists of 24 transmembrane segments and forms the pore through which ions pass into the cell. The calcium channel consists of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. There are multiple isoforms of each of these proteins, either encoded by different genes or the result of alternative splicing of transcripts. The protein encoded by this gene binds to and is inhibited by dihydropyridine. Alternative splicing results in many transcript variants encoding different proteins. [provided by RefSeq] Function: 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-1C gives rise to L-type calcium currents. Long-lasting (L-type) calcium channels belong to the 'high-voltage activated' (HVA) group. They are blocked by dihydropyridines (DHP), phenylalkylamines, benzothiazepines, and by omega-agatoxin-IIIA (omega-Aga-IIIA). They are however insensitive to omega-conotoxin-GVIA (omega-CTx-GVIA) and omega-agatoxin-IVA (omega-Aga-IVA). Calcium channels containing the alpha-1C subunit play an important role in excitation-contraction coupling in the heart. The various isoforms display marked differences in the sensitivity to DHP compounds. Binding of calmodulin or CABP1 at the same regulatory sites results in an opposit effects on the channel function. Subunit: Voltage-dependent calcium channels are multisubunit complexes, consisting of alpha-1, alpha-2, beta and delta subunits in a 1:1:1:1 ratio. The channel activity is directed by the pore-forming and voltage-sensitive alpha-1 subunit. In many cases, this subunit is sufficient to generate voltage-sensitive calcium channel activity. The auxiliary subunits beta and alpha-2/delta linked by a disulfide bridge regulate the channel activity. Interacts with CACNA2D4. Interacts (via the N-terminus and the C-terminal C and IQ motifs) with CABP1. The binding via the C motif is calcium independent whereas the binding via IQ requires the presence of calcium and is mutually exclusive with calmodulin binding. The binding to the cytoplasmic N-terminal domain is calcium independent but is essential for the channel modulation. Interacts (via C-terminal CDB motif) with CABP5; in a calcium-dependent manner. Subcellular Location: Membrane; Multi-pass membrane protein. Cell membrane. Note=The interaction between RRAD and CACNB2 regulates its trafficking to the cell membrane. Tissue Specificity: Expressed in brain, heart, jejunum, ovary, pancreatic beta-cells and vascular smooth muscle. Overall expression is reduced in atherosclerotic vascular smooth muscle. Post-translational modifications: Phosphorylation by PKA activates the channel. DISEASE: Defects in CACNA1C are the cause of Timothy syndrome (TS) [MIM:601005]. TS is a disorder characterized by multiorgan dysfunction including lethal arrhythmias, webbing of fingers and toes, congenital heart disease, immune deficiency, intermittent hypoglycemia, cognitive abnormalities and autism. Defects in CACNA1C are the cause of Brugada syndrome type 3 (BRGDA3) [MIM:611875]. A heart disease characterized by the association of Brugada syndrome with shortened QT intervals. Brugada syndrome is a tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram (ECG). It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs (called ventricular fibrillation), the individual will faint and may die in a few minutes if the heart is not reset. Similarity: Belongs to the calcium channel alpha-1 subunit (TC 1.A.1.11) family. CACNA1C subfamily. Database links: Entrez Gene: 775 Human Entrez Gene: 12288 Mouse Entrez Gene: 100144322 Rabbit Omim: 114205 Human SwissProt: Q13936 Human SwissProt: Q01815 Mouse SwissProt: P15381 Rabbit Unigene: 118262 Human Unigene: 436656 Mouse Unigene: 9827 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. L型鈣通道廣泛分布于心肌細胞膜上,尤其T管上含量最為豐富,是心肌細胞膜的主要鈣通道類型。L型鈣通道的開閉主要受膜電位變化的影響,是電壓依賴性鈣通道,激活電位-40~-30mV,失活電位-20mV。L型鈣通道開放后持續(xù)的時間長較長,激活占時20~30ms,失活更慢(100~300ms),又稱為慢鈣通道。 |
1、抗體溶解方法 | |
2、抗體修復(fù)方式 | |
3、常用試劑的配制 | |
4、免疫組化操作步驟 | |
5、免疫組化問題解答 | |
6、Western Blotting 操作步驟 | |
7、Western Blotting 問題解答 | |
8、關(guān)于肽鏈的設(shè)計 | |
9、多肽的溶解與保存 | |
10、酶標抗體效價測定程序 | |
| 国产亚洲精品成人a v久久网站 | 国产午夜精品一区二区三区视频 | 91在线精品国产乱码一二三软件 | 97人人添人人澡人人爽亚洲正品 | 黑人玩弄人妻一区二区三区视频 | 四川性BBB搡BBB爽爽爽小说 | 午夜国产A久久片亚洲最大 影音先锋中文字幕在线观看 | 精品人妻伦一二三区久久春菊 | 少妇性BBB搡BBB爽爽爽影院 | 高清无码波多野结衣 | 国产精品第一国产精品 | 韩国国产在线视频 | 国产真实亲子伦脏话对白免费影视 | 婷婷在线观看视频 | 成人AV动漫在线观看 | 国产精品福利视频 | 精品国产一区二区久久伦理 | 红杏成人性A片免费看 | 亚洲精品中文字幕乱码三区 | 亚州精品一区二区三区黄久 | 一级毛片黄久久久免费看A片 | 天天影视色欲综合插插插 | 吉根柚莉爱在线乱码亚洲 | 在线播放偷拍一区精品张丽 | 秋山静香一区二区三区网站 | 日本AⅤ毛片无码 9 2 1 5蜜桃 | 免费看无码一级A片放24小时 | 东北女人无套内谢视频 | 红桃成人网站在线观看 | 国产又粗又猛又爽又 | 真实人妻互换毛片视频 | 特级婬片A片AAA毛片咕噜咕噜 | 黄色视频中文字幕黄色 | 成人无码电影AV一区二区 | 欧美成人精品一区二区三区 | 二区三区日韩成人AV | 伦伦影院午夜理论片痴汉 | 中文字幕高清乱码免费 | 麻豆精品视频免费观看 | 丰满的岳 6699 |