HisPur™ Ni-NTA Superflow Agarose
HisPur™ Ni-NTA Superflow Agarose
Thermo Scientific™

HisPur™ Ni-NTA Superflow Agarose

Thermo Scientific HisPur Ni-NTA Superflow Agarose is a nitrilotriacetic acid (NTA) modified Superflow 6 support charged with divalent nickel (Ni+2)Read more
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Catalog NumberQuantity
2521410 mL
252171 L
2521550 mL
25216250 mL
Catalog number 25214
Price (USD)
161.00
Each
Add to cart
Quantity:
10 mL
Request bulk or custom format
Price (USD)
161.00
Each
Add to cart
Thermo Scientific HisPur Ni-NTA Superflow Agarose is a nitrilotriacetic acid (NTA) modified Superflow 6 support charged with divalent nickel (Ni+2) designed for FPLC purification of poly-histidine-tagged proteins.

Features of HisPur Ni-NTA Superflow Agarose:

High capacity—binds greater than 20 mg of His-tagged GFP per mL of resin at a linear flow rate of 300 cm/hour
High purity—provides greater than 80% purity of eluted fractions when used to purify from lysates
Versatile—can be used to purify proteins under native and denaturing conditions
Robust—highly crosslinked beads tolerate linear flow rates up to 1200 cm/hour
Compatible—maintains function in a wide variety of chemicals and pH conditions
Cost effective—competitively priced resin is stable through multiple cycles of cleaning and reuse

HisPur Ni-NTA Superflow Agarose is a highly crosslinked, durable resin that does not compress at flow rates used for medium- or large-scale FPLC purifications. The resin holds up well to a variety of chemicals and pH values, and is compatible with common clean-in-place procedures. Compared to cobalt and other ligands used for immobilized metal affinity chromatography (IMAC), nickel provides greater capacity for His-tagged protein purification. HisPur Ni-NTA Superflow Agarose exhibits a high dynamic binding capacity across a range of flow rates, making it an excellent choice for larger scale purifications.

Applications:
• Medium- to large-scale FPLC purification of polyhistidine tagged proteins

Affinity chromatography is often used as a quick and easy approach for the purification of recombinant proteins. One such method of purification involves the binding of a poly-histidine tag to a divalent metal cation that has been coordinated by a chelator immobilized on a beaded support. For immobilized metal affinity chromatography (IMAC) purification of His-tagged proteins, the type of bead, chelator, and metal immobilized influences purity, yield, and flow rate performance of these purifications.

HisPur Ni-NTA Superflow Agarose is a nitrilotriacetic acid (NTA) modified Superflow 6 support charged with divalent nickel (Ni+2) designed for FPLC purification of poly-histidine-tagged protein. To demonstrate performance, 6xHis-GFP was over expressed in a 100L reactor and the cell mass was collected in multiple fractions. A portion of the biomass (240g) was lysed with 2L of lysis buffer supplemented with Thermo Scientific Halt Protease Inhibitor (Part No. 78439). The lysate was clarified and split into two fractions. The target protein was then purified using HisPur Ni-NTA Superflow Agarose and a leading competitor's resin in equivalent 200 mL packed bead columns. Total yield, recovery, and purity (>80%) were nearly identical for both resins, and more than 4 grams of target protein was purified in less than 3 hours.

More Product Data
Performance characterization of HisPur Ni-NTA Superflow Agarose

Related Products
HisPur™ Ni-NTA Resin
WARNING: Cancer – www.P65Warnings.ca.gov
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Capacity (Metric)20 mg His-Tagged GFP Binding per mL Resin
FormLiquid Suspension
Product LineHisPur™
Quantity10 mL
TargetHis-Tagged Protein
TypeAgarose
Stationary PhaseDivalent Nickel, Metal Chelate
FormatBottle
Column TypeAffinity, Agarose Resin
Unit SizeEach
Contents & Storage
Store at 4°C

Frequently asked questions (FAQs)

Are there other sequences that can bind to nickel more tightly than 6xHis-tagged proteins and how can they be eluted.

Yes, 7xHis-tagged proteins, proteins naturally high in histidine, and other combinations of His and other amino acids will bind. To elute them, you have to increase the concentration of imidazole. Generally these peptides will not contaminate your fraction since they remain on the column. However after multiple uses of the same column, these peptides may reduce the binding capacity of the column.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Can ProBond or Ni-NTA beads be used for large-scale preparations?

ProBond and Ni-NTA beads can be used in FPLC columns. However, the beads can only withstand low pressure (~43.5 psi max).

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.