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Fig 1.

Preparation scheme of the IgG-enriched plasma fraction.

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Table 1.

Properties and specifications (or range) of the IgG-enriched plasma fraction.

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Fig 2.

Zone electrophoresis.

A: Patterns of 5 consecutive batches of minipool IgG-enriched plasma fractions (Minipool IgG batches B1 to B5) and control IgG (C) showing the separation between albumin (Alb) and alpha-1 (α-1), alpha-2 (α-2), bêta- (β) and gamma- (γ) proteins. B: densitographic analysis showing the percentage (%) of albumin, alpha-1, alpha-2, bêta, and gamma proteins in 5 batches (B1–B5) of minipool IgG. Control: control IgG.

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Fig 3.

Sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

Patterns of 10 consecutive batches of minipool IgG-enriched plasma fractions (Minipool IgG batches B1 to B10) and control IgG (C) under non-reducing (A) or reducing (B) conditions. Control: control IgG; IgG: immunoglobulin G; Alb: albumin. MW: molecular weight markers (kDa).

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Table 2.

Log removal factors of HIV-1, BVDV, and PRV during caprylic acid treatment (duplicate experiments).

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Table 2 Expand

Table 3.

Percent increase in body weight of rats (3 groups of 7 rats) treated with saline, commercial IgG, or minipool IgG.

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Table 3 Expand