Aptamers
(核酸适配体)
Aptamers are short single-stranded DNA or RNA that can bind to variety of targets, such as proteins, peptides, carbohydrates, and other molecules, by virtue of their tertiary structure, rather than their sequence. The aptamers have a high affinity to target protein similar to antibodies. Compared to antibodies, however, aptamers are small in size and have additional advantages, including improved transport into the cells and lower cost.
Cat. No. |
Product Name |
CAS No. |
Purity |
Chemical Structure |
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- HY-147080
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Avacincaptad pegol sodium
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1491144-00-3 |
98.53% |
Avacincaptad pegol (ARC1905) sodium 是一种偶联了 40 KDa PEG 的核酸适配体。Avacincaptad pegol sodium 靶向 补体因子5 (C5) ,抑制 C5 剪切为 C5a 和 C5b,限制炎症刺激和补体膜攻击复合物 (MAC),且被用于研究与年龄相关的黄斑变性 (AMD)。Avacincaptad pegol sodium 通过靶向补体级联中的下游因子,限制了不规则细胞凋亡,同时保留了补体系统的早期步骤。Avacincaptad pegol sodium 可治疗 Geographic atrophy (GA) 小鼠。
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Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA ((2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-Gm-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-Am-Gm-Gm-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-A-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-Gm-(3′→3′)-dT) 5′-[6-[[(2,3-dihydroxypropoxy)carbonyl]amino]hexyl hydrogen phosphate], sodium salt (2:1:39)
Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA ((2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-Gm-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-Am-Gm-Gm-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-A-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-Gm-(3′→3′)-dT) 5′-[6-[[(2,3-dihydroxypropoxy)carbonyl]amino]hexyl hydrogen phosphate], sodium salt (2:1:39)
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- HY-147081
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AS 1411
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301636-59-9 |
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AS 1411 (AGRO-100) 是一种靶向核蛋白的寡核苷酸适配体。AS 1411 通过影响含核蛋白复合物的活性抑制肿瘤细胞增殖,并可作为载体将纳米颗粒、寡核苷酸及小分子精准递送至癌细胞。AS 1411 在 DU145 前列腺癌细胞中,减少 PRMT5 表达以抑制肿瘤生长。AS 1411 在 MCF-7 乳腺癌细胞中,则通过阻断核蛋白与 bcl-2 mRNA 的结合发挥作用。AS 1411 偶联金纳球能在体外抑制乳腺癌细胞增殖,也可以在小鼠模型中抑制乳腺癌细胞增殖,具备穿越血脑屏障的能力且组织毒性低。
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DNA, d(G-G-T-G-G-T-G-G-T-G-G-T-T-G-T-G-G-T-G-G-T-G-G-T-G-G)
DNA, d(G-G-T-G-G-T-G-G-T-G-G-T-T-G-T-G-G-T-G-G-T-G-G-T-G-G)
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- HY-147081A
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DNA, d(G-G-T-G-G-T-G-G-T-G-G-T-T-G-T-G-G-T-G-G-T-G-G-T-G-G), sodium salt
DNA, d(G-G-T-G-G-T-G-G-T-G-G-T-T-G-T-G-G-T-G-G-T-G-G-T-G-G), sodium salt
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- HY-109561
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Pegaptanib sodium
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222716-86-1 |
98.09% |
Pegaptanib sodium 是一种靶向血管内皮生长因子 (VEGF)-165 的 RNA适配体。 Pegaptanib 可用于新生血管型老年性黄斑变性的研究。
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Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ester with RNA ((2′-deoxy-2′-fluoro)C-Gm-Gm-A-A-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-Am-Gm-(2′-deoxy-2′-fluoro)U-Gm-Am-Am-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)C-Am-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-Gm-(3′→3′)-dT) 5′-[5-[[2,6-bis(carboxyamino)-1-oxohexyl]amino]pentyl hydrogen phosphate] (2:1), sodium salt
Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ester with RNA ((2′-deoxy-2′-fluoro)C-Gm-Gm-A-A-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-Am-Gm-(2′-deoxy-2′-fluoro)U-Gm-Am-Am-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)C-Am-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-Gm-(3′→3′)-dT) 5′-[5-[[2,6-bis(carboxyamino)-1-oxohexyl]amino]pentyl hydrogen phosphate] (2:1), sodium salt
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- HY-153999
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BT200
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BT200 是偶联聚乙二醇的核酸适配体 BT100,可抑制 von Willebrand Factor(VWF) 与血小板糖蛋白GPIb的结合,预防动脉血栓形成。
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PEG40K‐NH‐mGmCmCmAmGmGmGmAmCmCmUmAmAmGmAmCmAmCmAmUmGmUmCmCmCmUmGmGmC‐idT
PEG40K‐NH‐mGmCmCmAmGmGmGmAmCmCmUmAmAmGmAmCmAmCmAmUmGmUmCmCmCmUmGmGmC‐idT
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- HY-153785
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NH2-C6-ARC186 sodium
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NH2-C6-ARC186 sodium 是一种可以偶联到其他肽或分子的、带 NH2-C6 接头的 ARC186 (HY-153098)。ARC186 是一种适体和高效补体抑制剂,通过阻断转化酶催化的 C5 活化起作用。
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NH2-C6-fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGfUfCfUmGmAmGfUfUfUAfCfCfUmGfCmG-3T, sodium salt
NH2-C6-fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGfUfCfUmGmAmGfUfUfUAfCfCfUmGfCmG-3T, sodium salt
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- HY-148100A
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Emapticap pegol sodium
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Emapticap pegol sodium 是促炎趋化因子 C-C 基序配体 2 (CCL2) 的抑制剂。Emapticap pegol sodium 是一种 40 个核苷酸的寡核苷酸适体,在人 (NOX-E36) 和小鼠 (mNOX-E36) 中具有不同的 Spiegelmers (L-RNA 适配子) 形式。
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Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA β-L-(G-C-A-C-G-U-C-C-C-U-C-A-C-C-G-G-U-G-C-A-A-G-U-G-A-A-G-C-C-G-U-G-G-C-U-C-U-G-C-G) 5′-[6-[[2-[(2-hydroxyacetyl)(2-hydroxyethyl)amino]acetyl]amino]hexyl hydrogen phosphate] (2:1), sodium salt
Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA β-L-(G-C-A-C-G-U-C-C-C-U-C-A-C-C-G-G-U-G-C-A-A-G-U-G-A-A-G-C-C-G-U-G-G-C-U-C-U-G-C-G) 5′-[6-[[2-[(2-hydroxyacetyl)(2-hydroxyethyl)amino]acetyl]amino]hexyl hydrogen phosphate] (2:1), sodium salt
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- HY-153480A
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ARC19499 sodium
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ARC19499 sodium 是一种核酸适配体, 与组织因子通路抑制剂(TFPI)特异性结合,阻断 TFPI 对 factor Xa 和 TF/factor VIIa 复合物的抑制作用。ARC19499 sodium 纠正血友病A和B血浆中的凝血酶生成,并恢复凝血。
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RNA, (Gm-Gm-Am-Am-Um-Am-Um-Am-dC-Um-Um-Gm-Gm-dC-Um-dC-Gm-Um-Um-Am-Gm-Gm-Um-Gm-dC-Gm-Um-Am-Um-Am-Um-Am-(3′→3′)-dT), 5′-(6-aminohexyl hydrogen phosphate), sodium salt
RNA, (Gm-Gm-Am-Am-Um-Am-Um-Am-dC-Um-Um-Gm-Gm-dC-Um-dC-Gm-Um-Um-Am-Gm-Gm-Um-Gm-dC-Gm-Um-Am-Um-Am-Um-Am-(3′→3′)-dT), 5′-(6-aminohexyl hydrogen phosphate), sodium salt
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- HY-153098
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ARC186
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ARC186 是一种未偶联 40KDa PEG 的核酸适配体,其核酸序列与 Avacincaptad pegol (ARC1905) 的一致。Avacincaptad pegol 是高效的补体抑制剂,通过阻断转化酶催化的C5 激活发挥作用。
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fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGfUfCfUmGmAmGfUfUfUAfCfCfUmGfCmG-3T
fCmGfCfCGfCmGmGfUfCfUfCmAmGmGfCGfCfUmGmAmGfUfCfUmGmAmGfUfUfUAfCfCfUmGfCmG-3T
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- HY-148457
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Avacincaptad pegol
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1613641-69-2 |
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Avacincaptad pegol 是一种核酸适配体,可用作 C5 补体抑制剂,减少炎症相关的视网膜色素上皮 (RPE) 损伤。Avacincaptad pegol caqn 可用于研究 stargardt 黄斑营养不良 (STGD1) 和地理萎缩 (GA)。
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Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA ((2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-Gm-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-Am-Gm-Gm-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-A-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-Gm-(3′→3′)-dT) 5′-[6-[[(2,3-dihydroxypropoxy)carbonyl]amino]hexyl hydrogen phosphate] (2:1)
Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA ((2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-Gm-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-Am-Gm-Gm-(2′-deoxy-2′-fluoro)C-G-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-Am-Gm-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-(2′-deoxy-2′-fluoro)U-A-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-Gm-(3′→3′)-dT) 5′-[6-[[(2,3-dihydroxypropoxy)carbonyl]amino]hexyl hydrogen phosphate] (2:1)
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- HY-147079
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Egaptivon pegol
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934868-74-3 |
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Egaptivon pegol (ARC1779) 是一种核酸适配体,阻碍 von Willebrand Factor(VWF)与血小板 GPIb 受体结合。Egaptivon pegol具有抗血栓作用。
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Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ester with RNA (Gm-Cm-Gm-Um-dG-dC-dA-Gm-Um-Gm-Cm-Cm-Um-Um-Cm-Gm-Gm-Cm-dC-Gm-sp-dT-Gm-dC-dG-dG-dT-Gm-Cm-dC-Um-dC-dC-Gm-Um-dC-Am-Cm-Gm-Cm-(3′→3′)-dT) 5′-[6-(carboxyamino)hexyl hydrogen phosphate]
Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ester with RNA (Gm-Cm-Gm-Um-dG-dC-dA-Gm-Um-Gm-Cm-Cm-Um-Um-Cm-Gm-Gm-Cm-dC-Gm-sp-dT-Gm-dC-dG-dG-dT-Gm-Cm-dC-Um-dC-dC-Gm-Um-dC-Am-Cm-Gm-Cm-(3′→3′)-dT) 5′-[6-(carboxyamino)hexyl hydrogen phosphate]
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- HY-153480
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ARC19499
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1350667-54-7 |
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ARC19499 是一种核酸适配体, 与组织因子通路抑制剂(TFPI)特异性结合,阻断 TFPI 对 factor Xa 和 TF/factor VIIa 复合物的抑制作用。ARC19499 纠正血友病A和B血浆中的凝血酶生成,并恢复凝血。
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RNA, (Gm-Gm-Am-Am-Um-Am-Um-Am-dC-Um-Um-Gm-Gm-dC-Um-dC-Gm-Um-Um-Am-Gm-Gm-Um-Gm-dC-Gm-Um-Am-Um-Am-Um-Am-(3′→3′)-dT), 5′-(6-aminohexyl hydrogen phosphate)
RNA, (Gm-Gm-Am-Am-Um-Am-Um-Am-dC-Um-Um-Gm-Gm-dC-Um-dC-Gm-Um-Um-Am-Gm-Gm-Um-Gm-dC-Gm-Um-Am-Um-Am-Um-Am-(3′→3′)-dT), 5′-(6-aminohexyl hydrogen phosphate)
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- HY-160049
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BC15 aptamer sodium
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BC15 aptamer sodium 是靶向癌性肝组织中高表达的、细胞内蛋白 hnRNP A1 的 ssDNA 适体。BC15 aptamer sodium 特异性识别乳腺癌细胞,可用于探测其他病理类型乳腺癌组织中的癌细胞。
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DNA, 5'-GCAATGGTACGGTACTTCCTGTGGCGAGGTAGGTGGGGTGTGTGTGTATCCAAAAGTGCACGCTACTTTGCTAA-3', sodium salt
DNA, 5'-GCAATGGTACGGTACTTCCTGTGGCGAGGTAGGTGGGGTGTGTGTGTATCCAAAAGTGCACGCTACTTTGCTAA-3', sodium salt
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- HY-160060
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MA3 aptamer sodium
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MA3 aptamer sodium 是靶向粘蛋白 MUC1、86 个碱基长度的 DNA 适体。MA3 aptamer sodium 可与粘蛋白 1 (MUC1) 的肽表位结合,Kd 为 38.3 nM,与白蛋白的交叉反应性极小。
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DNA, 5'-AACCGCCCAAATCCCTAAGAGTCGGACTGCAACCTATGCTATCGTTGATGTCTGTCCAAGCAACACAGACACACTACACACGCACA-3', sodium salt
DNA, 5'-AACCGCCCAAATCCCTAAGAGTCGGACTGCAACCTATGCTATCGTTGATGTCTGTCCAAGCAACACAGACACACTACACACGCACA-3', sodium salt
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- HY-148100
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Emapticap pegol
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1390630-22-4 |
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Emapticap pegol 是促炎趋化因子 C-C 基序配体 2 (CCL2) 的抑制剂。Emapticap pegol 是一种 40 个核苷酸的寡核苷酸适体,在人 (NOX-E36) 和小鼠 (mNOX-E36) 中具有不同的 Spiegelmers (L-RNA 适配子) 形式。
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Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA β-L-(G-C-A-C-G-U-C-C-C-U-C-A-C-C-G-G-U-G-C-A-A-G-U-G-A-A-G-C-C-G-U-G-G-C-U-C-U-G-C-G) 5′-[6-[[2-[(2-hydroxyacetyl)(2-hydroxyethyl)amino]acetyl]amino]hexyl hydrogen phosphate] (2:1)
Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ether with RNA β-L-(G-C-A-C-G-U-C-C-C-U-C-A-C-C-G-G-U-G-C-A-A-G-U-G-A-A-G-C-C-G-U-G-G-C-U-C-U-G-C-G) 5′-[6-[[2-[(2-hydroxyacetyl)(2-hydroxyethyl)amino]acetyl]amino]hexyl hydrogen phosphate] (2:1)
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- HY-153834
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GTI 2040
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236391-66-5 |
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GTI-2040 是一种硫代寡核苷酸,靶向人核糖核苷酸还原酶 R2 (ribonucleotide reductase R2) mRNA。GTI-2040 在体外通过下调 核糖核苷酸还原酶 R2 表达抑制癌细胞增殖,并在小鼠人类癌症异种移植模型中显著抑制肿瘤生长。
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DNA, d(P-thio)(G-G-C-T-A-A-A-T-C-G-C-T-C-C-A-C-C-A-A-G)
DNA, d(P-thio)(G-G-C-T-A-A-A-T-C-G-C-T-C-C-A-C-C-A-A-G)
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- HY-153836
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Anivamersen
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959716-29-1 |
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Anivamersen 是一种 RNA 核酸适配体,可逆转凝血因子 factor Ixa 抑制剂 pegnivacogin 的抗凝作用。Pegnivacogin(一种凝血因子IXa的RNA适体抑制剂)和 Anivamersen (一种互补序列反转寡核苷酸)构成了一种新型抗凝系统REG1。
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RNA, (Cm-Gm-Cm-Gm-Gm-Um-Am-Um-Am-Gm-Um-Cm-Cm-Am-Cm)
RNA, (Cm-Gm-Cm-Gm-Gm-Um-Am-Um-Am-Gm-Um-Cm-Cm-Am-Cm)
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- HY-153835
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Pegnivacogin
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959716-28-0 |
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Pegnivacogin 是一种新型的 RNA 核酸适配体,靶向凝血因子 factor IXa 的抑制剂,具有抗凝作用。Pegnivacogin 和 Anivamersen(是 Pegnivacogin 的互补序列寡核苷酸)组成新型抗凝系统REG1。
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Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ester with RNA (Gm-Um-Gm-Gm-Am-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)U-Am-Am-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-Um-G-Cm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Cm-Cm-Am-Cm-(3′→3′)-dT) 5′-[6-[[2,6-bis(carboxyamino)-1-oxohexyl]amino]hexyl hydrogen phosphate] (2:1)
Poly(oxy-1,2-ethanediyl), α-hydro-ω-methoxy-, 5′-ester with RNA (Gm-Um-Gm-Gm-Am-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)U-Am-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)C-Gm-(2′-deoxy-2′-fluoro)U-Am-Am-(2′-deoxy-2′-fluoro)U-Gm-(2′-deoxy-2′-fluoro)C-Um-G-Cm-(2′-deoxy-2′-fluoro)C-(2′-deoxy-2′-fluoro)U-Cm-Cm-Am-Cm-(3′→3′)-dT) 5′-[6-[[2,6-bis(carboxyamino)-1-oxohexyl]amino]hexyl hydrogen phosphate] (2:1)
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- HY-160042
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AFP aptamer sodium
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AFP aptamer sodium 是特异性靶向肝癌生物标志物甲胎蛋白 (AFP) 的核酸适体。AFP aptamer sodium 可作为 AFP 的识别分子,线性检测范围为 12.5-800 ng/mL。
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DNA, 5'-GGCAGGAAGACAAACAAGCTTGGCGGCGGGAAGGTGTTTAAATTCCCGGGTCTGCGTGGTCTGTGGTGCTGT-3', sodium salt
DNA, 5'-GGCAGGAAGACAAACAAGCTTGGCGGCGGGAAGGTGTTTAAATTCCCGGGTCTGCGTGGTCTGTGGTGCTGT-3', sodium salt
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- HY-160043
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AL6 aptamer sodium
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AL6 aptamer sodium 是体外化学合成的短链核酸适体。AL6 aptamer sodium 可特异性靶向 血管生成素 (Ang),用于 Ang 的特异性检测。AL6 aptamer 与 Ang 结合,使 AL6 aptamer 上荧光团的旋转运动变得更慢。通过检测 AL6 aptamer/Ang 的各向异性可定量待测液中 Ang 的浓度。
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DNA, 5'-CGGACGAATGCTTTGATGTTGTGCTGGATCCAGCGTTCATTCTCA-3', sodium salt
DNA, 5'-CGGACGAATGCTTTGATGTTGTGCTGGATCCAGCGTTCATTCTCA-3', sodium salt