Protein Isolation & Purification

MCLAB’s McBead™-6 magnetic stand is designed for efficient and simple separation of paramagnetic beads from 1.5-2 mL tubes. Extremely strong magnets are utilized for rapid magnetic response and separation. The magnetic stand is applicable for a wide selection of experiments relating to magnetic beads.

Recombinant Protein A is an immunoglobulin-binding protein derived from the cell wall of the bacterium Staphylococcus aureus. It is comprised of five homologous Ig-binding domains that fold into a three-helix bundle. Each domain is able to bind proteins from many of mammalian species, most notably IgGs. Protein A binds with high affinity to human IgG1 and IgG2 as well as mouse IgG2a and IgG2b.

SDS Low Molecular Weight Running Buffer is formulated for separating small- to medium-sized proteins on TrenX^TM gels.

Contains 100% active components and is a mixture of organic non - silicone polypropylene based polyether dispersions. Can be sterilized repeatedly.

Ni²⁺, Co²⁺, Cu²⁺, or Zn²⁺ charged nitrilotriacetic acid (NTA) coupled to Agarose CL-6B via a stable and uncharged long ether hydrophilic spacer arm, and offers high binding capacity and minimal non-specific binding.

25,000 U, 100 U/μl

500 μg,1 mg/ml

MCLAB’s McBead™-15 magnetic stand is designed for efficient and simple separation of paramagnetic beads from 15 mL tubes. Extremely strong magnets are utilized for rapid magnetic response and separation. The magnetic stand is applicable for a wide selection of experiments relating to magnetic beads.

Recombinant Protein G is an immunoglobulin-binding protein derived from the cell wall of certain strains of beta-hemolytic Streptococci. It binds with high affinity to the Fc portion of various classes and subclasses of immunoglobulins from a variety of species.

SDS High Molecular Weight Running Buffer is formulated for separating medium- to large-sized proteins on TrenXTM gels.

Used in proteomics and protein chromatography, amino acid agarose is prepared by covalently coupling of amino acid through a 17 atom stable and uncharged ether hydrophilic linkage to highly cross-linked 6% agarose with bead mean diameter of 90 um.

25% Triton X-100 is a commonly used detergent in laboratories.

Ni²⁺, Co²⁺, Cu²⁺, or Zn²⁺ charged iminodiacetic acid (IDA) coupled to Agarose CL-6B via a stable and uncharged long ether hydrophilic spacer arm, and offers high binding capacity and minimal non-specific binding.

1 mg, 1mg/ml

10 mg, 10 mg/ml

MCLAB’s McBead™-50 magnetic stand is designed for efficient and simple separation of paramagnetic beads from 50 mL tubes. Extremely strong magnets are utilized for rapid magnetic response and separation. The magnetic stand is applicable for a wide selection of experiments relating to magnetic beads.

Recombinant Protein G, HRP Conjugated (haptoglobin-related protein) is an immunoglobulin-binding protein derived from the cell wall of certain strains of beta-hemolytic Streptococci. It binds with high affinity to the Fc portion of various classes and subclasses of immunoglobulins from a variety of species.

MCLAB's premixed solution allows the user to perform fast staining on SDS-PAGE gels for protein analysis. This staining solution is nonhazardous and does not require the use of methanol and acetic acid for destaining. Protein bands become visible within minutes and the whole process takes 30 minutes.

Epoxy-activated Agarose is a pre-activated affinity chromatography support for the immobilization of a variety of biomolecules that contain nucleophiles, such as hydroxyl, amino, or thiol groups. These groups couple to the epoxy groups on the support, which is then used for the purification of proteins, carbohydrates, or DNA.

TRITON X-114 is used in biochemical applications to solubilize and separate proteins due to its low cloud point (23 °C).

0.5 mg, 2mg/ml