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Goat Anti-Swine IgG (H+L) Polyclonal Antibody

Cat. No.VD10H58

Product TypeAnimal-targeted Antibodies

Size

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Product Overview

O16H58 polyclonal antibody is specific for Swine IgG(H⁄L). It was purified by affinity chromatography on Protein A from tissue culture supernatant. It can be applied for ELISA.

Specifications

Application ELISA

Clonality Polyclonal Antibody

Classification Primary Antibody

Clone O16H58

Host Goat

Target Species Swine

Species Reactivity Swine

Specificity Swine IgG (H+L)

Isotype IgG

Immunogen Purified Swine IgG

Purification Affinity chromatography Purified

Purity ≥ 90% (SDS-PAGE)

Concentration 1.0 mg/mL

Conjugation Unconjugated

Preservative and Stabilizer 0.09% Sodium azide (NaN₃)

Buffer Phosphate buffered saline

Physical State Liquid

Target Information

IgG, also known as Immunoglobulin G is the most abundant antibody in serum, and is critical for humoral immunity. IgG plays an important role in opsonizing microbes for phagocytosis and killing, activating the complement cascade, and neutralizing many bacterial endotoxins and viruses. Swine IgG (heavy and light chains) antibody could react specifically with porcine IgG and with light chains common to other pig immunoglobulins.

Target Swine IgG (H+L)

Target Synonym Immunoglobulin G; IgG (H+L)

Shipping and Storage

This product is shipped at ambient temperature. It is recommended to aliquot and store at 2-8°C on receipt (up to 12 months).

Documents

Datasheet

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

User Note

DO NOT FREEZE. This product should be stored undiluted. Should this product contain a precipitate we recommend microcentrifugation before use.

References

Kesa, Gun, et al. "Comparison of ELISpot and FluoroSpot in the analysis of swine flu-specific IgG and IgA secretion by in vivo activated human B cells." Cells 1.2 (2012): 27-34.