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技術(shù)文章您現(xiàn)在的位置:首頁 > 技術(shù)文章 > Broadpharm知識(shí)課堂什么是生物素化發展契機?What is Biotinylation?

Broadpharm知識(shí)課堂什么是生物素化溝通機製?What is Biotinylation?

更新時(shí)間:2024-10-19   點(diǎn)擊次數(shù):1560次

生物素(Biotin)為B族維生素之一工藝技術,又稱維生素H長足發展、維生素B7著力提升、輔酶R(Coenzyme R)等具體而言。生物素是一種水溶性維生素貢獻法治,屬于B族維生素的一種。

生物素化落到實處,也稱為生物素標(biāo)記服務水平,是將生物素共價(jià)連接到生物分子(如蛋白質(zhì)、抗體技術創新、肽規則製定、寡核苷酸和其他大分子)的過程。該反應(yīng)是快速優化服務策略、特異性的關規定,并且由于生物素體積小 (MW = 244.31) 而不太可能干擾生物分子的自然功能。

生物素與鏈霉親和素和親和素特異性結(jié)合兩個角度入手,形成具有強(qiáng)親和力 (Kd建強保護, ~ 10-14 mol/L) 和快速接通速率的復(fù)合物。即使在高/低 pH 值生產效率、高溫使命責任、高鹽濃度等惡劣條件下,復(fù)合物也非常穩(wěn)定使用。

生物素-親和素和鏈霉親和素系統(tǒng)廣泛用于靶抗原/細(xì)胞的檢測和分離合規意識。這些應(yīng)用包括免疫測定(ELISA 和 Western 是常規(guī)應(yīng)用)、親和色譜有效性、沉降測定創新內容、超分子構(gòu)建、靶向癌細(xì)胞進(jìn)行藥物遞送等廣泛關註。最近善於監督,基于生物素-(strept)親和素相互作用和磁珠的蛋白質(zhì)/細(xì)胞分離的應(yīng)用需求不斷增加。


Broadpharm知識(shí)課堂什么是生物素化深入實施?What is Biotinylation?

Biotinylation, also known as biotin labeling, is the process of covalently attaching biotin(s) to biomolecules: such as proteins, antibodies, peptide, oligonucleotide, and other macromolecules. The reaction is rapid, specific and is unlikely to disturb the natural function of the biomolecules due to the small size of biotin (MW = 244.31).

Biotin specifically binds to streptavidin and avidin to form a complex with an extremely high affinity (Kd, ~ 10-14 mol/L) and fast on-rate. The complexes are very stable under even extreme conditions such as high/low pH, high temperature, high salt concentrations, etc.

Biotin-avidin and streptavidin systems are widely used in detection and separation of target antigens/cells. These applications include immunoassays (ELISAs and Westerns being the most popular applications), affinity chromatography, pull-down assays, supramolecular construction, targeting of cancer cells for drug delivery, and many others. Recently, there are increasing application demands for protein/cell separation based on biotin-(strept)avidin interaction and magnetic beads.


Broadpharm知識(shí)課堂什么是生物素化至關重要?What is Biotinylation?

Figure 1. biotin labeled antibody binds with streptavidin or avidin (four binding site available, only one is shown to binding to biotin).


Biotinylation Chemistry

For biotinylation chemistry, the most common reactions involve amines with biotin-NHS ester and click chemistry of azide with an alkyne (e.g. DBCO), as shown in Figure 2.


Broadpharm知識(shí)課堂什么是生物素化?What is Biotinylation?
Figure 2. NHS-amine chemistry (A) and click chemistry between azide-DBCO (B).


Biotinylation Reagent in Biotin Labeling

The selection of biotinylation reagent should consider a few factors: target functional group, water solubility, cell membrane permeability, cleavability, and length of the reagent.

The functional groups can be click chemistry reactive, amine reactive, carbonyl reactive, carboxyl reactive, and sulfhydryl reactive (Figure 3). There are also reversible and cleavable biotinylation reagents to help with the specific elution of biotinylated proteins.

Pegylated biotin reagents are particularly attractive due to their water solubility, no toxicity, and low immunogenic properties. Monodispersed PEGs have a well-defined chain length, allowing for specific biotin-based complexes to be designed and studied.


Broadpharm知識(shí)課堂什么是生物素化?What is Biotinylation?
Figure 3. Examples of BroadPharm's Pegylated biotinylation reagent with R 1 and R 2 options for functional groups.


In addition, BroadPharm provides desthiobiotin products for special application, such as affinity purification. Desthiobiotin is a modified form of biotin that binds less tightly to avidin and streptavidin than biotin while still providing excellent specificity. Unlike biomolecules that are labeled with biotin, proteins and other targets labeled with desthiobiotin can be eluted under a soft, mild elute conditions to avoid denaturing the protein of interest.

BroadPharm is a leader of biotinylation reagents that help advance our customer's research, and offers a variety of pegylated and non-pegylated biotinylation reagents to meet your requirement.

Journal Reference:

1. Cull and Schatz, "Biotinylation of proteins in vivo and in vitro using small peptide tags", Methods in Enzymology, 326, (2000): 430-440

2. Minde, et al., "Biotin proximity tagging favours unfolded proteins and enables the study of intrinsically disordered regions", Communications Biology, 3, 38, (2020): 1-13



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