Horse IgG (Fc) (31C-CH0804)
Purified Horse IgG (Fc)
|Synonyms||Horse Immunoglobulin G (Fc)|
|Applications||ELISA, IHC, WB|
SDS-PAGE analysis of Horse IgG (Fc) (31C-CH0804)
Lane 1: Horse IgG F(c) Fragment – Reduced. Lane 2: Horse IgG F(c) Fragment – Non-reduced. Load: 1.0 ug per lane. Predicted/Observed Size: Reduced- 25 kDa, Non-Reduced- 50 kDa.
|Method of Purification||Horse IgG (Fc) was purified by delipidation, salt fractionation, ion exchange chromatography followed by dialysis.|
|Form & Buffer||Supplied in liquid formfrom20 mM Potassium Phosphate, 150 mM Sodium Chloride, pH 7.2, with 0.01% NaN3 as a preservative.|
Usage & Assay Information
|Usage Recommendations||To be optimized by end user|
Storage & Safety
|Storage||Store at 4 deg C for short term storage, aliquot and freeze at -20 deg C for long term storage. Avoid repeated freeze/thaw cycles.|
|Biohazard Information||This product contains sodium azide as preservative. Although the amount of sodium azide is very small appropriate care must be taken when handling this product.|
|Biological Significance||Immunoglobulin G (IgG) are antibody molecules. Each IgG is composed of four peptide chains - two heavy chains and two light chains. Each IgG has two antigen binding sites. Other Immunoglobulins may be described in terms of polymers with the IgG structure considered the monomer. The Fc regions of IgGs bear a highly conserved N-glycosylation site. The N-glycans attached to this site are predominantly core-fucosylated diantennary structures of the complex type. In addition, small amounts of these N-glycans also bear bisecting GlcNAc and alpha-2,6-linked sialic acid residues.|
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