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Mouse Anti-Porcine Hemopexin Monoclonal Antibody

Cat. No.VD8N413

Product TypeAnimal-targeted Antibodies

Size

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Product Overview

BioVenic mouse monoclonal antibody is specific for hemopexin. It is affinity purified by protein G. It can be applied to WB, IHC, IF-P, FC and ELISA assays of hemopexin.

Specifications

Application WB; IHC; IF-P; FC; ELISA

Clonality Monoclonal

Classification Primary Antibody

Clone G9N13

Host Mouse

Target Species Porcine

Species Reactivity Porcine

Specificity Hemopexin

Isotype IgG1

Immunogen Recombinant protein of hemopexin

Purification Protein G Purified

Concentration 1700 μg/mL

Conjugation Unconjugated

Preservative and Stabilizer 0.02% Sodium Azide

Buffer Phosphate Buffered Saline with 50% Glycerol, pH 7.3

Physical State Liquid

Target Information

Porcine hemopexin (pHPX) is a serum glycoprotein found in pigs that plays a vital role in heme metabolism. It is responsible for the transport and scavenging of free heme, a molecule that can be toxic to cells if not properly managed. Heme, a component of hemoglobin, is released during the breakdown of red blood cells and must be safely sequestered to prevent oxidative damage and inflammation. pHPX binds to heme with high affinity, forming a stable complex that is then taken up by liver cells, where the heme is either stored, reused, or degraded. This process is essential for maintaining heme homeostasis and preventing the harmful effects of free heme on tissues.

Target Hemopexin

Target Synonym HPX; Beta-1B-glycoprotein

Gene ID 396998

UniProt ID P50828

Shipping and Storage

This product is shipped with ice gel packs. Store at -20°C (up to 12 months) on receipt.

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.

References

Schaer, Dominik J., et al. "Haptoglobin, hemopexin, and related defense pathways-basic science, clinical perspectives, and drug development." Frontiers in physiology 5 (2014): 415.