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Rabbit anti-Human COL4A6 Polyclonal Antibody

The antibody against COL4A6 was raised in Rabbit using the recombinant protein of human COL4A6 as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-08024A

The antibody against COL4A6 was raised in Rabbit using the recombinant protein of human COL4A6 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-08024A ClonalityPolyclonal
Host SpeciesRabbitTarget NameCOL4A6
Target SynonymsDFNX6; DELXq22.3; CXDELq22.3; COL4A6FormLiquid
Species ReactivityRatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive SamplesRat uterusApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant protein of human COL4A6.Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ14031
Background Information
  • Uniprot Id

    Q14031

  • Target Species

    Human

  • Target Name

    COL4A6

  • Target Full Name

    Collagen alpha-6(IV) chain

  • Target Function

    Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen.

  • Target Involvement

    Deafness, X-linked, 6 (DFNX6)

  • Target Subcellular Location

    Secreted, extracellular space, extracellular matrix, basement membrane.

  • Target Protein Families

    Type IV collagen family

  • Target Synonyms

    COL4A6Collagen alpha-6(IV) chain

  • Target Background

    This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Alternative splicing results in multiple transcript variants encoding different isoforms.

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