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Rabbit anti-Human C6 Polyclonal Antibody

The antibody against C6 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 586-934 of human C6 (NP_000056.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-01323A

The antibody against C6 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 586-934 of human C6 (NP_000056.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-01323A ClonalityPolyclonal
Host SpeciesRabbitTarget NameC6
Target SynonymsC6FormLiquid
Species ReactivityMouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesMouse liver, Mouse lung, Rat lungApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 586-934 of human C6 (NP_000056.2).Target SpeciesHuman
Uniprot IDP13671Immunogen Sequence
Background Information
  • Uniprot Id

    P13671

  • Target Species

    Human

  • Target Name

    C6

  • Target Full Name

    Complement component C6

  • Target Function

    Constituent of the membrane attack complex (MAC) that plays a key role in the innate and adaptive immune response by forming pores in the plasma membrane of target cells.

  • Target Involvement

    Complement component 6 deficiency (C6D)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Complement C6/C7/C8/C9 family

  • Target Synonyms

    AW111623; C6; CO6_HUMAN; Complement component 6; Complement component C6

  • Target Background

    This gene encodes a component of the complement cascade. The encoded protein is part of the membrane attack complex that can be incorporated into the cell membrane and cause cell lysis. Mutations in this gene are associated with complement component-6 deficiency. Transcript variants encoding the same protein have been described.

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