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HSA
BSA
RSA
Fibrinogen
HDL
IgG-Fc
Transferrin
The ProteomeLab IgY-R7 Single-
Component Proteome Partitioning
kits specifically remove any of
these highly abundant proteins.
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ProteomeLab™ IgY Single-Component Proteome Partitioning
Kits for HSA, BSA, RSA, Fibrinogen, HDL,
IgG-Fc, Transferrin
The ProteomeLab IgY Proteome Partitioning Spin Column kits are based on
affinity columns using avian antibody (IgY)-antigen interactions and optimized
buffers for sample loading, washing, eluting and regenerating. They are designed
to work with the ProteomeLab SP sample preparation system and specifically
remove a targeted protein from biological fluids such as serum, plasma, and
cerebral spinal fluid (CSF) so as to enhance discovery and validation of
biomarkers, drug targets, and therapeutic proteins and antibodies.
The targeted abundant protein is removed in a highly selective fashion by the
immobilized specific IgY capture reagent when complex biological samples are
passed through the column. Selective immunoaffinity partitioning provides an
enriched pool of lower abundant proteins for downstream proteome analysis, as
well as enabling the investigator to analyze isoforms of the captured protein
and trace materials that are physiologically associated with the target protein.
Both the unbound material in the flow-through fraction and the highly abundant
protein in the bound/eluted fraction can be collected and further fractionated
with the ProteomeLab PF 2D System. Our technology uses physiological buffers for
binding and washing, and avoids urea and other chaotropic agents for elution
that can precipitate at low temperature.
Each kit provides enough reagents for 200 cycles, with a plasma or serum
capacity per cycle of 20 µL to 125 µL depending on the species and kit selected.
Cleaner Capture
Since the polyclonal IgYs are avian, the Fc region of the antibody does not
bind mammalian complement factors, Rheumatoid Factor, IgM, Fc receptor and
Protein A or G, a known issue related to capture with mammalian antibodies.
Coupled with high specificity across multiple epitopes, you get very specific
binding across species while achieving very clean capture. Partitioning
efficiency is typically greater then 99.5%. The SDS-PAGE on the left highlights
whole serum in lane #1, serum with just albumin partitioned out by Proteome-Lab
IgY-HSA SC chemistry in lane #2, and the isolated/partitioned albumin captured
cleanly in lane #3.
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