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C7 Rabbit Polyclonal Antibody

Product Specifications

Background

C7 is a component of the complement system. It participates in the formation of Membrane Attack Complex (MAC) . People with C7 deficiency are prone to bacterial infection. [provided by RefSeq, Jul 2008], disease:Defects in C7 are a cause of component C7 deficiency (C7D) [MIM:217070]. Patients with C7D suffer from recurrent bacterial infections, predominantly from Neisseria meningitidis., function:C7 is a constituent of the membrane attack complex. C7 binds to C5b forming the C5b-7 complex, where it serves as a membrane anchor., online information:C7 mutation db, PTM:C7 has 28 disulfide bridges., similarity:Belongs to the complement C6/C7/C8/C9 family., similarity:Contains 1 EGF-like domain., similarity:Contains 1 LDL-receptor class A domain., similarity:Contains 1 MACPF domain., similarity:Contains 2 Sushi (CCP/SCR) domains., similarity:Contains 2 TSP type-1 domains., subunit:Monomer or dimer; as a C5b-7 complex it can also form multimeric rosettes.

Product Name Alternative

C7; Complement component C7

Gene Name

C7

Gene ID

730

Swiss Prot

P10643

Host

Rabbit

Reactivity

Human, Rat, Mouse

Clonality

Polyclonal

Conjugation

Unconjugated

Applications

WB, IHC, ICC/IF, ELISA

Field of Research

Complement and coagulation cascades; Prion diseases; Systemic lupus erythematosus

Purification

Affinity purification

Dilution

WB 1:500-1:2000, IHC 1:100-1:300, ICC/IF 1:50-1:200, ELISA 1:5000-1:20000

Form

Liquid

Buffer

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

Modification

Unmodified

Molecular Weight

93kDa

Storage Conditions

Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.

Isotype

IgG

Available Sizes

Curated Selection

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