MFAP3 Proteins, cDNA Clones Research Reagents

MFAP3 (Microfibril Associated Protein 3), located on 5q33.2, is a Protein Coding gene. The gene produces a 40165 Da protein composed of 362 amino acids. MFAP3 is widely expressed in the placenta, urinary bladder, and other tissues. It does not appear to share homology with any other known protein. MFAP3 is a candidate gene for heritable diseases affecting microfibrils. Diseases such as Lutembacher's Syndrome and Postural Orthostatic Tachycardia Syndrome are associated with MFAP3. The related pathways of MFAP3 include Degradation of the extracellular matrix and Elastic fibre formation.

MFAP3 Protein (1)

    MFAP3 cDNA Clone (13)

    BC026244

    クローニングベクター cDNA 製品

    In lentiviral vector

    MFAP3 qPCR Primer (1)

    MFAP3 Lysate (1)

      MFAP3 の背景知識

      MFAP3 (Microfibril Associated Protein 3) is a Protein Coding gene. The human gene encoding MFAP3 has a very simple structure, containing only two translated exons encoding a protein of 362 amino acids. The gene was found to be located on chromosome 5q32-q33.2, near the locus 5q21-q31 reported for the fibrillin gene, FBN2, which has been linked to congenital contractural arachnodactyly. MFAP3 is widely expressed in the placenta, urinary bladder, and other tissues. It does not appear to share homology with any other known protein. MFAP3 is a candidate gene for heritable diseases affecting microfibrils. Diseases associated with MFAP3 include Lutembacher's Syndrome and Postural Orthostatic Tachycardia Syndrome.

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