生物素抗体标记试剂盒（Sulfo-NHS-LC-Biotin）专为高效可靠的抗体标记而设计，仅需60分钟即可获得即用型标记抗体，且操作时间极短。试剂盒包含抗体标记所需的所有必要试剂，包括 Sulfo-NHS-LC-生物素试剂、缓冲液及离心式脱盐柱。盒内提供的 Sulfo-NHS-LC- 生物素试剂是一种中等长度、水溶性的生物素化试剂，适用于标记含有伯胺基的抗体、蛋白质及其他分子。NHS活化生物素可在pH 7–9的缓冲液中与伯氨基（-NH2）高效反应，形成稳定的酰胺键（图1）。试剂盒中的 离心式脱盐柱 用于从过量生物素试剂中纯化生物素化抗体，回收率达70–95%。本试剂盒所含试剂足以完成10次、每次100 μg抗体的生物素化反应。生物素化抗体可通过亲和素或链霉亲和素探针，应用于ELISA、Western Blot、免疫荧光/免疫细胞化学（IF/ICC）或流式细胞术等检测。Aladdin提供一系列高性能链霉亲和素偶联物，用于检测生物素化抗体的性能。
图1 Sulfo-NHS-LC-Biotin标记抗体原理图
Sulfo-NHS-LC-Biotin 特点
- 蛋白质标记——对抗体进行生物素化，便于通过链霉亲和素树脂或探针进行固定、纯化或检测
- 细胞表面标记——仅标记完整细胞的表面蛋白；因该带负电荷试剂无法穿透细胞膜
- 胺基反应性——可与伯氨基（-NH2）（如赖氨酸侧链或多肽氨基末端）发生反应
- 水溶性——带电荷的磺基NHS基团相比普通NHS酯类化合物提高了试剂的水溶性
- 不可逆结合——形成永久性酰胺键；间隔臂不可断裂
- 中等长度——间隔臂（添加至目标分子的总长度）为22.4埃；在足够长度（减少生物素结合的位阻效应）与适度分子量之间实现优异平衡
其他所需试剂
1. 离心机
2. 用于标记的所需抗体（不含BSA或任何载体蛋白）。
3. PBS缓冲液（pH 7.2-7.4）。
重要须知
1. 纯化的抗体缓冲液中不得含有铵离子或者伯胺组分，例如Tris、甘氨酸、乙醇胺、三乙胺、谷胱甘肽或咪唑，所有这些物质都会显著抑制蛋白质标记。
2. 用于标记的抗体需经过纯化，不含有BSA或明胶等稳定剂。
3. 抗体浓度1-2mg/mL最佳，浓度低于1mg/mL, 标记效率可能会降低，浓度过高，抗体体积会过少，不利于纯化回收。
4. 脱盐柱建议一次性使用。
5. 试剂盒使用之前，需将所有组分恢复至室温。
6. 荧光染料均存在淬灭问题，请尽量注意避光，以减缓荧光的淬灭。
使用说明
1. 缓冲液配制：
a) 1M NaHCO₃的配制。根据样品量配制适量的1M NaHCO₃溶液，如称取42mg NaHCO₃，加入0.5mL超纯水即得1M NaHCO₃溶液。NaHCO₃可维持标记反应体系的pH在7-9之间，提高标记效率。注：NaHCO₃溶液须现用现配。
2. 抗体标记
a) 如果待标记的抗体浓度≥1mg/mL，并且在适当的缓冲液中，则将其稀释至1mg/mL，并加入10%抗体体积的1M NaHCO₃缓冲液。如果抗体是从适当的缓冲液中冻干的粉末，通过向抗体中加入适量的0.1M NaHCO₃缓冲液来制备1mg/mL的抗体溶液。用去离子水将1M溶液稀释10倍，制备0.1M NaHCO₃缓冲液。
b) 将100μL抗体溶液转移到生物素试剂管中。盖上管盖，轻轻翻转几次，使生物素试剂完全溶解。
注意：为确保染料完全溶解，请将标签从生物素试剂管上撕下。
c) 将反应管室温避光反应1h。反应可以在振荡器或混合器上进行，建议上下翻转速度为25rpm。如果在反应过程中不使用混合仪器，则应每10分钟将反应溶液倒置混合一次。
注意：反应进行期间，可提前进行步骤3的操作，完成脱盐柱的平衡。
3. 脱盐柱预平衡
a) 松开脱盐柱盖子，折断柱子下端堵头，将脱盐柱置于配套的2mL收集管中。1000xg离心2分钟，丢弃离心下来的保存溶液，并将脱盐柱放回收集管中。
注意：使用非水平转头的情况下，由于离心会使树脂压实形成一个向上的斜面，该斜面的方向宜在后续步骤中保持，所以在脱盐柱外壳上的斜面向上位置做标记，在随后的离心步骤中需要调整好离心管的放入方向，确保离心后斜面的方向和位置不会改变。
b) 向脱盐柱树脂顶部加入500μL PBS，轻轻拧上脱盐柱上盖，1000×g离心2分钟，丢弃溶液，重复此步骤3次。
4. 生物素化抗体纯化
a) 将平衡后的脱盐柱转移至新的收集管中。小心的将反应管中的反应液加入脱盐柱中，盖上脱盐柱盖子，注意盖子轻轻拧上即可。
b) 脱盐柱1000xg离心2分钟，收集管中的流出即为所需收集的生物素化抗体。
5. 测定蛋白浓度（可选）
通过检测280nm吸光度检测抗体浓度。
6. 保存
a) 向标记后的蛋白中加入 0.05~0.2 % Proclin 300 或 0.05 %叠氮化钠，及蛋白稳定剂 (如 0.1 % BSA)，于 2~8°C 避光保存，可稳定保存半年。或加入等体积甘油于-20°C 存 储，可稳定保存半年。
The Sulfo-NHS-LC-Biotinylation Kit is designed for efficiency and reliability, delivering ready-to-use labeled antibody in just 60 minutes, with minimal hands-on time. The kit include all necessary reagents for antibody labeling, including Sulfo-NHS-LC-Biotin, buffer, and purification columns. The Sulfo-NHS-LC-Biotin reagent included in the kit is an intermediate-length, water-soluble biotinylation reagent for labeling antibodies, proteins, and other molecules that have primary amines. NHS-activated biotins react efficiently with primary amino groups (-NH2) in pH 7-9 buffers to form stable amide bonds (Fig 1). Spin columns included in the kit are used for purifying the biotinylated antibody from excess biotin reagent with yields of 70–95%. The kit contains sufficient reagents for 10 biotinylation reactions of 100 μg of antibody. The biotinylated antibody can be detected in ELISA, Western Blot, IF/ICC or Flow Cytometry application using avidin or streptavidin probes. Aladdin offers a series of high-performance streptavidin conjugates designed for detecting the performance of biotinylated antibodies.
Figure 1 Reaction of Sulfo-NHS-LC-Biotin with antibody
Features of Sulfo-NHS-LC-Biotin:
- Protein labeling—biotinylate antibodies to facilitate immobilization, purification or detection using streptavidin resins or probes
- Cell surface labeling—biotinylates only surface proteins of whole cells because the negatively charged reagent does not permeate cell membranes
- Amine-reactive—reacts with primary amines (-NH2), such as lysine side-chains, or the amino-termini of polypeptides
- Soluble—charged sulfo-NHS group increases reagent water solubility compared to ordinary NHS-ester compounds
- Irreversible—forms permanent amide bonds; spacer arm cannot be cleaved
- Medium length—spacer arm (total length added to target) is 22.4 angstroms; provides excellent balance between adequate length (minimal steric hindrance for biotin binding) and modest mass
Required materials not supplied
1. Microcentrifuge capable of 1,000 xg.
2. Desired antibody for labeling (free of BSA or any carrier protein).
3. PBS buffer (pH 7.2-7.4).
Important
1. The purified antibody should be in a buffer that does not contain primary amines (for example, ammonium ions, Tris, glycine, ethanolamine, triethylamine, glutathione) or imidazole. All of these substances significantly inhibit protein labeling.
2. Impure antibodies or antibodies stabilized with bovine serum albumin (BSA) or gelatin will not be labeled well.
3. Concentrate the antibody to ≥1 mg/mL.
4. Do not reuse the purification resin.
5. Before opening the vials, warm all components to room temperature.
6. The reactive dyes should be protected from prolonged exposure to light.
Instructions for Use
1. Prepare the reagents
a) Prepare a 1 M sodium bicarbonate solution—Prepare an appropriate amount of 1M NaHCO₃ solution based on the sample volume. For example, weigh 42mg of NaHCO₃ and add 0.5mL of ultrapure water to obtain a 1M NaHCO₃ solution. NaHCO₃ can maintain the pH of the labeling reaction system between 7-9, thereby improving labeling efficiency. Note: The NaHCO₃ solution must be prepared fresh before each use.
2. Label the antibody
a) If the antibody to be labeled has a concentration of ≥1 mg/mL and is in an appropriate buffer, dilute it to 1 mg/mL, and add a 10% volume of 1 M sodium bicarbonate buffer. If the antibody is a powder lyophilized from an appropriate buffer, prepare a 1 mg/mL solution of the antibody by adding an appropriate amount of 0.1 M sodium bicarbonate buffer to the antibody. Prepare 0.1 M sodium bicarbonate buffer by diluting the 1 M solution 10-fold with deionized water.
b) Transfer 100 μL of the antibody solution to the vial of biotin reagent. Cap the vial and gently invert it a few times to fully dissolve the biotin reagent.
Note: To visually ensure that the dye has fully dissolved, peel the label off the vial of biotin reagent.
c) Incubate the solution for 60 minutes at room temperature. The reaction can be carried out on a shaker or mixer, recommended speed for flipping up and down is 25rpm. If a mixing instrument is not used during the reaction process, the reaction solution should be mixed upside down every 10 minutes.
Note: During the incubation period, proceed to steps 3 below, to prepare a spin column for the purification of the labeled protein.
3. Prepare the spin column
a) Loosen the cap on a spin column, twist the tab off of the bottom, then place the column into a collection tube.
b) Centrifuge the column‑tube assembly at 1,000 x g for 2 minutes to remove the storage solution.
Note: When using a fixed-angle rotor, place a mark on the side of the column that faces away from the rotor center. For all subsequent centrifugation steps, place the column in the microcentrifuge with the mark facing away from the rotor center.
c) Discard the flowthrough, then place the column back into the collection tube.
d) Add 500 μL of PBS Buffer, then centrifuge the column‑tube assembly at 1,000 x g for 2 minutes to equilibrate the column. Repeat this step d) 3 times, discarding the buffer from the collection tube each time.
4. Purification with Desalting Column
a) Transfer the equilibrated column into a new collection tube.
b) Carefully pipette the entire reaction mixture onto the center of the column.
c) Centrifuge the column‑tube assembly at 1,000 × g for 2 minutes. The purified antibody conjugate is in the collection tube.
5. Determine the antibody concentration (Optional)
Determination of antibody concentration by measuring absorption at 280 nm.
6. Strorage
Add 0.05–0.2% Proclin 300 or 0.05% sodium azide, along with a protein stabilizer (such as 0.1% BSA), to the labeled protein. Store protected from light at 2–8°C for stable preservation up to six months. Alternatively, add an equal volume of glycerol and store at -20°C for stable preservation up to six months.
F2610352
危险品化学品经营许可证（带存储）