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Merck

LSKMAGN04

PureProteome NHS FlexiBind Magnetic Bead System

NHS FlexiBind beads are suitable for Immunoprecipitations, purifying nucleic acids, isolating cells and organelles, performing protein-protein interaction studies and many other applications.

同義詞:

Magnetic Bead System, NHS FlexiBind Bead System

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分類程式碼代碼:
41116133
eCl@ss:
32160405
NACRES:
NA.56

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形狀

liquid

包裝

pkg of 2 mL

製造商/商標名

PureProteome

技術

protein purification: suitable

粒徑

10 μm

容量

>17 μmol/mL, settled beads binding capacity (NHS)

運輸包裝

wet ice

儲存溫度

2-8°C

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本產品
LSKMAG1CBXLSKMAG03CBXLSKMAGH
form

liquid

form

slurry

form

slurry

form

liquid

packaging

pkg of 2 mL

packaging

pkg of 2 × 1 mL

packaging

pkg of 2 × 1 mL

packaging

pkg of 10 mL

manufacturer/tradename

PureProteome

manufacturer/tradename

PureProteome

manufacturer/tradename

PureProteome

manufacturer/tradename

PureProteome

technique(s)

protein purification: suitable

technique(s)

protein purification: suitable

technique(s)

protein purification: suitable

technique(s)

protein purification: suitable (histidine tagged recombinant protein)

particle size

10 μm

particle size

1 μm

particle size

0.3 μm

particle size

10 μm

capacity

>17 μmol/mL, settled beads binding capacity (NHS)

capacity

97–114 μmol/g, settled beads binding capacity (carboxylic acid

carboxylic acid

carboxylic acid)

capacity

89–175 μmol/g, settled beads binding capacity (carboxylic acid)

capacity

1-5.5 mg/mL, bead suspension binding capacity (protein)

一般說明

{TM="PureProteome"] NHS (N-Hydroxysuccinimide) FlexiBind Magnetic Beads provide researchers flexibility in binding the ligand of their choice. The only prerequisite is that the molecule must contain a primary free amine group. NHS FlexiBind beads are being used for the generation of custom affinity beads for binding to target ligands and protein purification.

應用

PureProteome NHS FlexiBind Magnetic Bead System has been used in co-immunoprecipitation[1] and affinity purification.[2]

法律資訊

PureProteome is a trademark of Merck KGaA, Darmstadt, Germany

象形圖

FlameExclamation mark

訊號詞

Danger

危險聲明

危險分類

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

標靶器官

Central nervous system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

53.6 °F - closed cup

閃點(°C)

12.0 °C - closed cup


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

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您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Ling Liu et al.
European journal of pharmacology, 858, 172520-172520 (2019-07-07)
The metabolic disorder of succinate in myocardial tissue during ischemia-reperfusion can lead to the myocardial oxidative injury. The activation of succinate dehydrogenase (SDH) plays a vital role in the process. Silent information regulator 5 (Sirt5), a nicotinamide adenine dinucleotide (NAD)-dependent
Zakhar O Shenkarev et al.
Journal of neurochemistry, 155(1), 45-61 (2020-03-31)
Lynx1 is a GPI-tethered protein colocalized with nicotinic acetylcholine receptors (nAChRs) in the brain areas important for learning and memory. Previously, we demonstrated that at low micromolar concentrations the water-soluble Lynx1 variant lacking GPI-anchor (ws-Lynx1) acts on α7-nAChRs as a

相關內容

Immunoprecipitation (IP) is a powerful technique for proteomic screening, biomarker discovery, and signaling network elucidation. It is frequently used to enrich target proteins from complex samples such as cell lysates or extracts. Traditional IP protocols use Protein A, Protein G or a mixture of Protein A and G coupled to a solid support resin, such as agarose beads, to capture an antigen/antibody complex in solution. As the number of samples increase, the traditional, manual IP method can be time-consuming. Processing of multiple IP reactions in parallel can introduce complexity, variability and pipetting errors, which may affect reproducibility.

Purification of recombinant proteins expressed in E.coli requires many time-consuming steps. To liberate the protein of interest, traditional bacterial lysis relies on the addition of lysozyme and a combination of sonication and repeated freeze/thaw cycles to break the bacterial cell wall. Disruption of the cell is accompanied by an increase in the viscosity of the suspension, due to the release of DNA. An endonuclease is added to digest the DNA, thus reducing the viscosity of the lysate. Finally, to render the lysate compatible with traditional purification methods, insoluble cell debris must be removed by centrifugation.

Traditionally, protein purification from E. coli consists of four distinct phases: harvest, bacterial cell lysis, lysate clarification and protein purification. Bacterial lysis typically requires several time-consuming, hands-on steps, such as freeze/thaw cycles and sonication. These harsh lysis techniques may negatively impact protein quality and contribute to sample-to-sample variability. To maintain protein activity and integrity, detergent-based lysis buffers are routinely used to avoid mechanical protein extraction methods. Regardless of the lysis method used, centrifugation is traditionally required to pellet unwanted cell debris and permit recovery of the clarified lysate. The final step, purification, is frequently performed using affinity media specific for expressed epitope tags. Agarose-based media have typically been used, either as a slurry in microcentrifuge tubes or packed into gravity-driven or spin columns. While easier to manipulate, columns are greatly affected by lysate consistency and carryover of cell debris, which can lead to clogging of the column frits.

PureProteome™ NHS FlexiBind magnetic beads offer you flexibility in binding your target ligand. The kit contains everything you need, and offers high binding capacities (NHS density > 17 μmoles/mL of settled beads) with high specificity due to covalent linkages. NHS FlexiBind is perfect for applications involving targets that do not have affinity for common preconjugated magnetic beads.

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