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Rabbit anti-Human MCTP2 Polyclonal Antibody

The antibody against MCTP2 was raised in rabbit using the Recombinant Human Multiple C2 and transmembrane domain-containing protein 2 protein (129-240AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, IHC, IF.

ADC-04848A

The antibody against MCTP2 was raised in rabbit using the Recombinant Human Multiple C2 and transmembrane domain-containing protein 2 protein (129-240AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, IHC, IF.

$299.00

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Specifications


Cat.No ADC-04848A ClonalityPolyclonal
Host SpeciesRabbitTarget NameMCTP2
Target SynonymsMCTP2Multiple C2 and transmembrane domain-containing protein 2 antibodyFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4Purification Method>95%, Protein G purified
ConjugateNon-conjugatedApplicationELISA, IF, IHC
StorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Multiple C2 and transmembrane domain-containing protein 2 protein (129-240AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ6DN12
Background Information
  • Uniprot Id

    Q6DN12

  • Target Species

    Human

  • Target Name

    MCTP2

  • Target Full Name

    Multiple C2 and transmembrane domain-containing protein 2

  • Target Function

    Might play a role in the development of cardiac outflow tract.

  • Target Involvement

    Heterozygosity for a 2.2-Mb deletion at chromosome 15q26.2, encompassing MCTP2, has been identified in a 10-year-old girl and her 3-year-old half brother, who had both coarctation of the aorta associated with dysmorphic features and ventricular septal defects. An intragenic MCTP2 duplication, leading to premature truncation (F697X) within the first transmembrane region of the protein, has also been observed in a male patient with a non-syndromic complex cardiac malformation involving coarctation, hypoplastic left heart, mitral atresia, bicuspid aortic valve and muscular ventricular septal defect. Although the link between left ventricular outflow tract malformations and MCTP2 could not be established, it has been proposed that defects in the MCTP2 gene may contribute to phenotype. This hypothesis is supported by the observation that Xenopus laevis embryos treated with MCTP2 morpholinos show no evidence of endocardial cushion formation at any level of the developing outflow tract (PubMed:23773997).

  • Target Subcellular Location

    Membrane; Multi-pass membrane protein.

  • Target Protein Families

    MCTP family

  • Target Synonyms

    MCTP2Multiple C2 and transmembrane domain-containing protein 2

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