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当前位置: 首页 > 产品中心 > peptide > Qiagen/Ni-NTA超流药筒/5个预先填充5 ml Ni-NTA超流的药筒:用于使用液相色谱系统自动纯化His标记的蛋白质/30761
商品详细Qiagen/Ni-NTA超流药筒/5个预先填充5 ml Ni-NTA超流的药筒:用于使用液相色谱系统自动纯化His标记的蛋白质/30761
Qiagen/Ni-NTA超流药筒/5个预先填充5 ml Ni-NTA超流的药筒:用于使用液相色谱系统自动纯化His标记的蛋白质/30761
Qiagen/Ni-NTA超流药筒/5个预先填充5 ml Ni-NTA超流的药筒:用于使用液相色谱系统自动纯化His标记的蛋白质/30761
商品编号: 30761
品牌: Qiagen
市场价: ¥12880.00
美元价: 7728.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Ni-NTA Superflow Cartridges

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For His-tagged protein purification using liquid chromatography systems

  • Most robust one-step purification over the widest range of conditions
  • High yields of high-purity protein, with up to 50 mg/ml
  • Fast, easy, and reproducible processing on any LC system

Ni-NTA Superflow, the most-cited resin used for purification of His-tagged proteins, is available in pre-filled 1 ml and 5 ml cartridges for automated purification on liquid chromatography systems such as the FPLC, ÄkTA, and BioLogic systems, or manual purification using a syringe.

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Cat No./ID:30761
Ni-NTA Superflow Cartridges (5 x 5 ml)
$644.00
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5 cartridges pre-filled with 5 ml Ni-NTA Superflow: for automated purification of His-tagged proteins using liquid chromatography systems
Cat No./ID:30765
Ni-NTA Superflow Cartridges (100 x 5 ml)
$9,969.00
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100 cartridges pre-filled with 5 ml Ni-NTA Superflow: for automated purification of His-tagged proteins using liquid chromatography systems
Ni-NTA Superflow Cartridges are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.

Product Details

9
Highly reproducible and reliable purification.
His-tagged pGAPase was purified in 10 sequential purification procedures. Column load was 10 ml aliquots of cleared E. coli cell lysate containing 30 mg spiked protein. Between purification runs the column was cleaned in place using 0.5 M NaOH. Groups of three samples show column load, flow-through, and peak elution fraction. M: markers.
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The extra coordination site (arrowed) in Ni-NTA binds nickel more tightly than IDA (the ligand used in many competitor resins).
9
Scalable purification of nanogram to gram amounts of His-tagged proteins.

See table "Micro to large-scale purification of IL-1β for a biopharmaceutical project."

9
Efficient one-step purification of His-tagged proteins using buffers containing a wide variety of additives.
The indicated protein was purified in buffers containing  [A]  reducing agent (10 mM DTT) and  [B]  detergent (1% n-dodecyl-β-D-maltoside)  [C]  Human GBP1 expressed in S. cerevisiae (data kindly provided by Julia Fres, Center for Molecular Medicine, Cologne University, Germany). M:markers; C: cleared lysate; F: flow-through; W: wash; L: lysate; S: soluble fraction; P: pellet; E: elution fractions.
9
Ni-NTA outperforms other resins to deliver high yields of high-purity protein.
Ni-NTA outperforms other resins to deliver high yields of high-purity protein. ERK2 was purified using a Ni-NTA Superflow Cartridge or the indicated resin from another supplier, according to manufacturer"s instructions. M: markers; C: cleared lysate; F: flow-through; W: wash; E: elution fractions.
9
An independent study shows that Ni-NTA loses less nickel than any other tested resin.
An independent study shows that Ni-NTA loses less nickel than any other tested resin. Fifty column volumes of buffer containing various additives was passed through a small column containing 100 μl resin from QIAGEN, Supplier G, S, or I. The flowthrough was pooled and a sample sent for analysis by inductively coupled plasma mass spectrometry (ICP-MS) at Dr.Weßling Laboratories, Bochum, Germany according to DIN EN ISO 17025. Native buffer: 50 mM Na phosphate; 300 mM NaCl; 10 mM imidazole, pH 8.0. Denaturing buffer: 100 mM Na phosphate; 10 mM Tris·Cl; 8 M urea.
Performance

Ni-NTA gives superior performance in delivering high yields of highly purified protein, in comparison to other resins (see figure Ni-NTA outperforms other resins to deliver high yields of high-purity proteins). An independent comparison with other commercially available nickel resins demonstrated that Ni-NTA Superflow shows the lowest level of nickel leaching (see figure An independent study shows that Ni-NTA loses less nickel than any other tested resin). The significance here is that if nickel is leached from the resin, the remaining charged ligands act as an ion exchanger and bind non-tagged proteins that will contaminate elution fractions. The higher stability of Ni-NTA means that even in the presence of 10 mM DTT it can be used to obtain fully active, high-purity proteins (see figure The extra coordination site in Ni-NTA binds nickel ion more tightly than IDA).

As shown in the table, purities are consistently high over all purification scales. Ni-NTA Superflow Cartridges form part of the comprehensive and complementary solutions for His-tagged protein offered by QIAGEN (see figure Scalable purification of nanogram to gram amounts of His-tagged proteins).

Micro- to large-scale purification of IL-1β for a biopharmaceutical project
MatrixMatrix volume Culture volume YieldRecovery (%)Purity*
Ni-NTA Magnetic Agarose Beads (micro-scale)100 μl 1 ml 33 μg ~90%~97%
Ni-NTA Superflow (small-scale) 500 μl 320 ml 6 mg ~80%~96%
Ni-NTA Superflow (medium-scale)10 ml 1.7 l109 mg ~80%~98%
Ni-NTA Superflow (large-scale)100 ml 18 l2 g>88%~97%
* Determined using Agilent Bioanalyzer (Protein 50 LabChip Kit)

Principle

Ni-NTA matrices are the affinity chromatography solution of choice for purifying His-tagged proteins (see figureEfficient one-step purification of His-tagged proteins). Their high stability means that they are compatible with a wide range of buffer components, including strong denaturants, detergents, and even reducing agents (see table Reagents compatible with the His/Ni-NTA interaction). This flexibility enables researchers to develop optimal purification schemes while still benefiting from the excellent separation characteristics delivered by Ni-NTA, often making a second chromatographic step unnecessary.

Reagents compatible with the His/Ni-NTA interaction.
Denaturants Detergents Reducing agents Others Salts Long-term storage
6 M Gu·HCl 2% Triton X-100 20 mM β-ME 50% glycerol 4 M MgCl2 Up to 30% ethanol
8 M urea 2% Tween 20 10 mM DTT 20% ethanol 5 mM CaCl2 or 100 mM NaOH
1% CHAPS 20 mM TCEP 20 mM 20 mM TCEP 20 mM imidazole 2 M NaCl
Procedure
The robust Superflow matrix allows flow rates up to 10 ml/min (1 ml cartridges) and 40 ml/min (5 ml cartridges), speeding the purification procedure and increasing throughput. The cartridges are quickly and easily connected to liquid chromatography systems or a syringe for manual purification. The purification process is highly reproducible, guaranteeing the same high quality protein preparations time after time (see figure Highly reproducible and reliable purification).
Applications

Ni-NTA matrices can be used to scale up purification of His-tagged proteins for structural studies (e.g., using protein crystallography or NMR), or to produce gram amounts for biopharmaceutical production.

Specifications

Features
Specifications
ApplicationsProteomics
Bead size60-160 µm
Binding capacityUp to 50 mg/ml
FPLCYes
Gravity flow or spin columnFPLC or syringe
N- or C-terminal tagBoth
ProcessingManual/Automated
ScaleLarge scale
Start materialCell lysate
Support/matrixSuperflow
Tag6xHis tag
YieldUp to 50 mg (1 ml cartridge), up to 250 mg (5 ml cartridge)

Product Resources

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FAQs (4)
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What is the binding capacity of the Ni-NTA Superflow Cartridges?
FAQ ID -1603
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How fast is the 6xHis-tagged protein purification process using Ni-NTA Superflow Cartridges?
FAQ ID -1605
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Can the Ni-NTA Superflow Cartridges and/or Strep-Tactin Cartridges be connected in series?
FAQ ID -1606
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Can the Ni-NTA and Strep-Tactin Superflow Cartridges be reused?
FAQ ID -1607
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Kit Handbooks (2)
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Ni-NTA Superflow Cartridge Handbook - (EN)
For manual or FPLC purification of His-tagged proteins
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(EN) - Important Note for Ni-NTA Users
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Instrument Technical Documents (1)
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Ni-NTA Superflow Cartridge Specifications - (EN)
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Technical Information (3)
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Complete solutions for membrane protein analysis - (EN)
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Critical factors for successful protein crystallization - (EN)
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Reliable purification of GST-, His-, and Strep-tagged proteins - (EN)
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Scientific Posters (3)
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(EN) - New Ni-NTA Cartridges — the faster way to purer proteins
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(EN) - Novel cell-free expression system for synthesis of proteins used in structural analyses
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(EN) - Process Development: Scaling Up Human IL-1b Production, Tag Removal, and X-Ray Crystallography
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Supplementary Protocols (1)
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Adding QIAGEN® FPLC™ cartridges to ÄKTA UNICORN™ software - (EN)
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Quick-Start Protocols (2)
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Automated Purification of 6xHis-tagged Proteins from E. coli Using Ni-NTA Superflow under Native Conditions (EN)
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Ni-NTA Agarose Purification of 6xHis-tagged Proteins from E. coli under Native Conditions (EN)
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Safety Data Sheets (2)
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MSDS Ni-NTA Superflow Cartridges (5 x 5 ml)
MSDS Ni-NTA Superflow Cartridges (100 x 5 ml)
References
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品牌介绍
QIAGEN是一家专业化致力于生物分子样品制备解决方案的跨国经营企业,总部位于德国。1984年,QIAGEN在德国成立,1996年在美国纽约纳斯达克上市。QIAGEN拥有超过1000项专利和认可证明,在18个国家设立了分公司,代理商服务国超过40个,在全球有超过400000的用户。QIAGEN提供的产品超过500类,包括各种试剂,耗材和自动化纯化工作站。这些产品用于样品采集,稳定,核酸或蛋白的分离,纯化和检测中,不仅广泛的应用于科研领域的各个方面,在生物技术,制药,法医研究,食品安全检测,畜牧业和分子诊断领域也得到了广泛的应用。QIAGEN产品的卓越品质和在应用中的出色表现使得其成为样品处理中标准的代名词。