HisPur™ Ni-NTA Magnetic Beads
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Invitrogen17万+抗体限时买二赠一,靶点广,灵活用!
HisPur™ Ni-NTA Magnetic Beads
Thermo Scientific™

HisPur™ Ni-NTA Magnetic Beads

Perform affinity purification of His-tagged fusion proteins in manual or automated formats with the high capacity nickel-IMAC Thermo Scientific™ HisPur Ni-NTA Magnetic Beads.
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Catalog NumberQuantity
8883210 mL
888312 mL
Catalog number 88832
Price (CNY)
11,065.00
Each
Add to cart
Quantity:
10 mL
Request bulk or custom format
Price (CNY)
11,065.00
Each
Add to cart

Thermo Scientific HisPur Ni-NTA Magnetic Beads are high-capacity nickel-IMAC beads for affinity purification of His-tagged fusion proteins in manual or automated formats.

Features of HisPur Ni-NTA Magnetic Beads:

  • High capacity—equivalent or higher binding capacity than Ni-NTA magnetic beads from other suppliers
  • Low nonspecific binding—the bead surface is pre-blocked and the protocol provides optimized buffers for purification
  • Fast—protocol is completed in 1 hour
  • Scalable—process microliter to milliliter sample volumes
  • Versatile—purify proteins using native or denaturing conditions
  • Reagent compatible—can be used with common cell lysis reagents and a variety of buffer additives
  • Multiple formats—protein coupling to the beads and downstream applications can be performed both manually and on an automated platform (e.g., Thermo Scientific KingFisher Instruments)

The blocked magnetic bead surface is derivatized with the nitrilotriacetic acid (NTA) chelation moiety and loaded with divalent nickel ions (Ni2+). The immobilized metal affinity chromatography (IMAC) beads provide high binding capacity with very low background. The HisPur Ni-NTA Magnetic Beads can be used both manually with a magnetic stand as well as with automated platforms such as the Thermo Scientific KingFisher Instruments for high-throughput needs.

HisPur Ni-NTA Magnetic Beads are used for small scale affinity purification as well as high-throughput screening of recombinant His-tagged proteins. The polyhistidine tag is the most popular affinity tag and typically consists of six consecutive histidine residues (6xHis). These tagged proteins are overexpressed in a number of different systems, most commonly in bacteria, and purified from cell lysates such as those prepared using B-PER Bacterial Protein Extraction Reagents. Purification of His-tagged proteins is achieved using a NTA chelate charged with nickel that coordinates with the histidine side chains. The NTA chelate contains four metal-binding sites which allow for low metal ion leaching and high binding capacity. The protocol for the HisPur Ni-NTA Magnetic Beads has been optimized to allow for high purity of the isolated His-tagged protein. Performance is equivalent to or better than Ni-NTA magnetic beads from other suppliers.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
ConcentrationSlurry: 12.5mg/mL, 1.25% solids
Ligand TypeNickel-NTA
Protein FormRecombinant
Quantity10 mL
TargetHis
Capacity (Metric)10 mL
Particle Size1 μm
Product LineHisPur
TypeMagnetic Affinity Bead
Unit SizeEach
Contents & Storage
Store at 4°C

Frequently asked questions (FAQs)

What should the typical protein recovery be when using the Probond Purification System or Ni-NTA Purification system?

Both systems are qualified by purifying 2 mg of myoglobin protein on a column and performing a Bradford assay. Protein recovery must be 75% or higher.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

What is the difference between HisPur Nickel Resin and HisPur Cobalt Resin?

Nickel has a higher affinity for histidines than does cobalt. It binds multiple histidines more tightly than cobalt, and requires more stringent conditions than is necessary for cobalt. The lower affinity of cobalt for multiple histidines typically results in less nonspecific binding of histidine-rich proteins that lack a his-tag compared to nickel resins.

HisPur Ni-NTA resin has a high capacity of up to 60 mg of 6xHis-tagged protein per milliliter. It is a versatile resin that can work under both native and denaturing conditions, and can also be used with a variety of lysis reagents and buffer additives.

HisPur Cobalt resin utilizes proprietary tetradentate chelating resin charged with cobalt. This system recovers highly purified protein with lower imidazole concentrations and has low metal leeching properties.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Citations & References (3)

Citations & References
Abstract
Structure and bioactivity of an insecticidal trans-defensin from assassin bug venom.
Authors:Walker AA,Chin YK,Guo S,Jin J,Wilbrink E,Goudarzi MH,Wirth H,Gordon E,Weirauch C,King GF
Journal:Structure (London, England : 1993)
PubMed ID:38889720
Disulfide-rich peptides such as defensins play diverse roles in immunity and ion channel modulation, as well as constituting the bioactive components of many animal venoms. We investigated the structure and bioactivity of U-RDTX-Pp19, a peptide previously discovered in venom of the assassin bug Pristhesancus plagipennis. Recombinant Pp19 (rPp19) was found ... More
Human serum-derived α-synuclein auto-antibodies mediate NMDA receptor-dependent degeneration of CNS neurons.
Authors:Garg P,Würtz F,Hobbie F,Buttgereit K,Aich A,Leite K,Rehling P,Kügler S,Bähr M
Journal:Journal of neuroinflammation
PubMed ID:38419079
BACKGROUND: Presence of autoantibodies against α-synuclein (α-syn AAb) in serum of the general population has been widely reported. That such peripheral factors may be involved in central nervous system pathophysiology was demonstrated by detection of immunoglobulins (IgGs) in cerebrospinal fluid and brain of Parkinson's disease (PD) patients. Thus, blood-borne IgGs ... More
Control of the antitumour activity and specificity of CAR T cells via organic adapters covalently tethering the CAR to tumour cells.
Authors:Stepanov AV,Xie J,Zhu Q,Shen Z,Su W,Kuai L,Soll R,Rader C,Shaver G,Douthit L,Zhang D,Kalinin R,Fu X,Zhao Y,Qin T,Baran PS,Gabibov AG,Bushnell D,Neri D,Kornberg RD,Lerner RA
Journal:Nature biomedical engineering
PubMed ID:37798444
On-target off-tumour toxicity limits the anticancer applicability of chimaeric antigen receptor (CAR) T cells. Here we show that the tumour-targeting specificity and activity of T cells with a CAR consisting of an antibody with a lysine residue that catalytically forms a reversible covalent bond with a 1,3-diketone hapten can be ... More