Recombinant Mouse Complement Factor H/CFH Protein (His Tag) | PKSM041346

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575-PKSM041346
€579.00
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Description

Recombinant Mouse Complement Factor H/CFH Protein (His Tag) | PKSM041346 | Gentaur US, UK & Europe Disrtribition

Synonyms: Complement factor H;Protein beta-1-H;CFH; beta-1-H-globulin

Active Protein: N/A

Activity: Recombinant Mouse Complement factor H is produced by our Mammalian expression system and the target gene encoding Ser875-Val1252 is expressed with a 6His tag at the C-terminus.

Protein Construction: Recombinant Mouse Complement factor H is produced by our Mammalian expression system and the target gene encoding Ser875-Val1252 is expressed with a 6His tag at the C-terminus.

Fusion Tag: C-His

Species: Mouse

Expressed Host: Human Cells

Shipping: This product is provided as lyophilized powder which is shipped with ice packs.

Purity: > 90 % as determined by reducing SDS-PAGE.

Endotoxin: < 1.0 EU per μg as determined by the LAL method.

Stability and Storage: Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.

Molecular Mass: 43.4 kDa

Formulation: Lyophilized from a 0.2 μm filtered solution of 20 mM Tris, 150mM NaCl, pH8.0.

Reconstitution: Please refer to the printed manual for detailed information.

Background: Complement factor H(CFH) is a 155 kDa glycoprotein that functions as a cofactor in the inactivation of C3b by factor I. It also increases the rate of dissociation of the C3bBb complex (C3 convertase) and the (C3b)NBB complex (C5 convertase) in the alternative complement pathway. CFH expressed by the liver and secreted in plasma. This recombinant protein corresponds to SCR15-20 which encompass the primary binding sites for heparin and C3b as well as for the peptide hormone adrenomedullin. Within SCR15-20, mouse Factor H shares 60% and 80% amino acid sequence identity with human and rat Factor H, respectively. Dozens of mutations clustered in SCR15-20 are associated with atypical hemolytic uremic syndrome, a disorder characterized by anemia, thrombocytopenia, and renal failure.

Research Area: N/A

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