LSKMAGHDKIT
PureProteome Human Albumin/Immunoglobulin Depletion Kit
The PureProteome Human Albumin/Immunoglobulin Depletion Kit is a magnetic bead based kit that enables high depletion efficiency of Albumin and all Immunoglobulins from human serum or plasma samples.
Synonym(s):
Protein Purification
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About This Item
UNSPSC Code:
41116133
eCl@ss:
32160405
NACRES:
NA.56
Recommended Products
packaging
kit of 12 mL beads
manufacturer/tradename
PureProteome
technique(s)
depletion: suitable (human serum/plasma)
protein purification: suitable
particle size
10 μm
shipped in
wet ice
storage temp.
2-8°C
Related Categories
General description
The PureProteome Human Albumin/Immunoglobulin Depletion Kit is a magnetic bead based kit that enables high depletion efficiency (typically >99%) of Albumin and all Immunoglobulins (i.e IgG, IgA, IgM, IgE and IgD) from human serum or plasma samples. The kit includes 12ml of premixed mag beads, 7ml of PBS buffer and an 8 pack of Amicon Ultra centrifugals for downstream buffer exchange or concentration if required.
Application
PureProteome Human Albumin/Immunoglobulin Depletion Kit has been used: to remove specific components from the serum sample for preparing protein stocks using capillary electrophoresis and depletion of all immunoglobulins from plasma.
Features and Benefits
- Matrix comprises of magnetic silica beads coated with polymers and coupled with antibody ligands.
- Beads have specific antibody ligands for recognizing and binding human serum albumin and immunoglobulins.
- Assists in the detection and analysis of proteins of interest.
Components
12 mL of premixed magnetic beads, 7mL of PBS buffer, and an 8-pack of Amicon Ultra-2 mLcentrifugal filters, 3K MWCO
Analysis Note
Depletion: >98% albumin, IgG, IgA, IgM, IgE & IgD depletion. Typical values are >99% depletion.
wgk_germany
WGK 2
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Daniel J Sobczynski et al.
Bioengineering & translational medicine, 2(2), 180-190 (2017-09-22)
The high abundance of immunoglobulins (Igs) in the plasma protein corona on poly(lactic-co-glycolic) acid (PLGA)-based vascular-targeted carriers (VTCs) has previously been shown to reduce their adhesion to activated endothelial cells (aECs) in human blood flow. However, the relative role of
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