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微管蛋白α (乙酰化Lys40)多克隆抗體
| 貨號(hào) | 品牌 | CAS | 規(guī)格 | 銷售價(jià)(RMB) | 折扣價(jià)(RMB) | 備注 | 數(shù)量 |
| ABP50115-100 μL | Abbkine | 無(wú) | 100μL | 1616 | 1616 | 無(wú) | |
| ABP50115-30μL | Abbkine | 無(wú) | 30μL | 739 | 739 | 無(wú) | |
| ABP50115-100μL | Abbkine | 無(wú) | 100μL | 1616 | 1616 | 無(wú) |
商品信息
| 產(chǎn)品英文名稱 | Tubulin α (Acetyl Lys40) Polyclonal Antibody |
| 免疫原 | 合成多肽：人源蛋白Tubulin α，乙?；嚯模行陌被釣镵40. |
| 宿主 | 兔 |
| 反應(yīng)性 | 人, 大鼠, 小鼠 |
| 應(yīng)用 | ELISA, IHC-P, WB |
| 實(shí)驗(yàn)建議 | 最佳的工作稀釋比例需要客戶摸索優(yōu)化。建議的起始嘗試的稀釋比為：WB：1:500-1:2000，IHC-p：1:100-300，ELISA：1:20000。 尚未在其他應(yīng)用中測(cè)試。 |
| 克隆性 | 多克隆 |
| 純化工藝 | 使用表位特異性的免疫原，通過(guò)親和層析，從兔抗血清中親和純化抗體。 |
商品屬性
| 產(chǎn)品形式 | 液體溶液 |
| 濃度 | 1 mg/ml |
| 儲(chǔ)存緩沖液 | 含有50％甘油，0.5％BSA和0.02％疊氮化鈉的PBS緩沖液。 |
| 保存建議 | 自發(fā)貨之日起，-20°C可穩(wěn)定保存1年。為最大限度的避免損失，請(qǐng)?jiān)诖蜷_管蓋之前融化抗體并離心。我們建議使用前分裝以避免反復(fù)凍融。 |
| 運(yùn)輸條件 | 藍(lán)冰運(yùn)輸 |
| 警告 | 本文列出的產(chǎn)品僅供研究使用，不適用于人類或臨床診斷。我們產(chǎn)品所推薦應(yīng)用，不是建議使用我們的產(chǎn)品去違反任何專利或許可證。對(duì)于使用本產(chǎn)品可能發(fā)生的專利侵權(quán)或其他違規(guī)行為，我們不承擔(dān)任何責(zé)任。 |
附加信息
| 背景 | Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulins. The genes encoding these microtubule constituents belong to the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes, which are highly conserved among species. TUBA1A encodes alpha tubulin and is highly similar to the mouse and rat Tuba1 genes. Northern blotting studies have shown that TUBA1A expression is predominantly found in morphologically differentiated neurologic cells. TUBA1A is one of three alpha-tubulin genes in a cluster on chromosome 12q. Mutations in TUBA1A cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly, mental retardation, and early-onset epilepsy and caused by defective neuronal migration. Alternative splicing results in multiple transcript variants encoding distinct isoforms. |
| 基因ID | 7846 |
| 別名 | TUBA1A; TUBA3; Tubulin alpha-1A chain; Alpha-tubulin 3; Tubulin B-alpha-1; Tubulin alpha-3 chain; TUBA1B; Tubulin alpha-1B chain; Alpha-tubulin ubiquitous; Tubulin K-alpha-1; Tubulin alpha-ubiquitous chain; TUBA1C; TUBA6;Tubulin alpha-6 chain; TUBA3C; TUBA2; TUBA3D; Tubulin alpha-3C/D chain; Alpha-tubulin 2; Alpha-tubulin 3C/D; Tubulin alpha-2 chain; TUBA4A; TUBA1; Tubulin alpha-4A chain; Alpha-tubulin 1; Testis-specific alpha-tubulin; |
| 其它 | 該抗體可檢測(cè)內(nèi)源蛋白 |
| 蛋白質(zhì)ID | Q71U36 |
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