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CFAD (Cleaved-Ile26) rabbit pAb

Catalytic activity: Selective cleavage of Arg-|-Lys bond in complement factor B when in complex with complement subcomponent C3b or with cobra venom factor. Disease: Defects in CFD are the cause of complement factor D deficiency [MIM: 134350]. This deficiency predisposes to invasive meningococcal disease. function: Factor D cleaves factor B when the latter is complexed with factor C3b, activating the C3bbb complex, which then becomes the C3 convertase of the alternate pathway. Its function is homologous to that of C1s in the classical pathway. online information: CFD mutation db, similarity: Belongs to the peptidase S1 family. similarity: Contains 1 peptidase S1 domain.

Product Specifications

Background

Catalytic activity:Selective cleavage of Arg-|-Lys bond in complement factor B when in complex with complement subcomponent C3b or with cobra venom factor., disease:Defects in CFD are the cause of complement factor D deficiency [MIM:134350]. This deficiency predisposes to invasive meningococcal disease., function:Factor D cleaves factor B when the latter is complexed with factor C3b, activating the C3bbb complex, which then becomes the C3 convertase of the alternate pathway. Its function is homologous to that of C1s in the classical pathway., online information:CFD mutation db, similarity:Belongs to the peptidase S1 family., similarity:Contains 1 peptidase S1 domain.

UniProt

P00746

Swiss Prot

P00746

Reactivity

Human; Rat; Mouse

Immunogen

Synthesized peptide derived from human CFAD (Cleaved-Ile26)

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Concentration

1 mg/ml

Dilution

WB 1:1000-2000 ELISA 1:5000-20000

Molecular Weight

25kD

Storage Conditions

-20°C/1 year

Observed Molecular Weight

25kD

Fragment

IgG

Subcellular Location

Secreted.

Other Product Names

Complement factor D (EC 3.4.21.46; Adipsin; C3 convertase activator; Properdin factor D)

Gene ID (Human)

1675

Available Sizes

Curated Selection

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