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Recombinant Human Microfibrillar-associated protein 5 (MFAP5)

Amino acids 22-173 constitute the expression domain of recombinant Human MFAP5. This MFAP5 protein is theoretically predicted to have a molecular weight of 33.3 kDa. This protein is generated in a e.coli-based system. Fusion of the N-terminal 6xHis-SUMO tag into the MFAP5 encoding gene fragment was conducted, allowing for easier detection and purification of the MFAP5 protein in subsequent stages.Human Microfibrillar-Associated Protein 5 (MFAP5) is involved in extracellular matrix (ECM) organization, interacting with elastin and fibrillin to contribute to tissue elasticity and stability. In vascular biology, MFAP5 regulates elastic fiber assembly, impacting arterial compliance. Its role in tissue development and repair makes MFAP5 relevant in regenerative medicine and wound healing research. In cancer biology, MFAP5 is implicated in tumor progression and metastasis, potentially serving as a prognostic marker. Investigating MFAP5 provides insights into ECM dynamics, vascular physiology, and cancer microenvironment, offering potential applications in cardiovascular research, tissue engineering, and cancer therapeutics.

ACP04063

Amino acids 22-173 constitute the expression domain of recombinant Human MFAP5. This MFAP5 protein is theoretically predicted to have a molecular weight of 33.3 kDa. This protein is generated in a e.coli-based system. Fusion of the N-terminal 6xHis-SUMO tag into the MFAP5 encoding gene fragment was conducted, allowing for easier detection and purification of the MFAP5 protein in subsequent stages.Human Microfibrillar-Associated Protein 5 (MFAP5) is involved in extracellular matrix (ECM) organization, interacting with elastin and fibrillin to contribute to tissue elasticity and stability. In vascular biology, MFAP5 regulates elastic fiber assembly, impacting arterial compliance. Its role in tissue development and repair makes MFAP5 relevant in regenerative medicine and wound healing research. In cancer biology, MFAP5 is implicated in tumor progression and metastasis, potentially serving as a prognostic marker. Investigating MFAP5 provides insights into ECM dynamics, vascular physiology, and cancer microenvironment, offering potential applications in cardiovascular research, tissue engineering, and cancer therapeutics.

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Specifications


Cat.No ACP04063 Target NameMFAP5
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range22-173aaMol Weight33.3kDa
Protein LengthFull Length of Mature ProteinPurityGreater than 90% as determined by SDS-PAGE.
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ13361
Background Information
  • Uniprot Id

    Q13361

  • Target Species

    Human

  • Target Name

    MFAP5

  • Target Full Name

    Microfibrillar-associated protein 5

  • Target Function

    May play a role in hematopoiesis. In the cardiovascular system, could regulate growth factors or participate in cell signaling in maintaining large vessel integrity. Component of the elastin-associated microfibrils.

  • Target Involvement

    Aortic aneurysm, familial thoracic 9 (AAT9)

  • Target Subcellular Location

    Secreted, extracellular space, extracellular matrix.

  • Target Protein Families

    MFAP family

  • Target Research Area

    Cancer

  • Target Synonyms

    AAT9; MAGP 2; MAGP-2; MAGP2; MFAP 5; MFAP-5; MFAP5; MFAP5_HUMAN; Microfibril associated glycoprotein 2; Microfibril-associated glycoprotein 2; microfibrillar associated protein 5; Microfibrillar associated protein 5 precursor ; Microfibrillar-associated protein 5; MP25

  • Target Background

    This gene encodes a 25-kD microfibril-associated glycoprotein which is a component of microfibrils of the extracellular matrix. The encoded protein promotes attachment of cells to microfibrils via alpha-V-beta-3 integrin. Deficiency of this gene in mice results in neutropenia. Alternate splicing results in multiple transcript variants encoding different isoforms.

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