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P4HA1 Antikörper (Middle Region)

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch P4HA1 in WB, IHC und IF. Es zeigt Reaktivität gegenüber Proben von Human.
Produktnummer ABIN7879544
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für P4HA1 Antikörper (Middle Region) (ABIN7879544)

Target

Alle P4HA1 Antikörper anzeigen
P4HA1 (Prolyl 4-Hydroxylase, alpha Polypeptide I (P4HA1))

Reaktivität

  • 31
  • 10
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 29
  • 3
  • 1
Kaninchen

Klonalität

  • 32
  • 1
Polyklonal

Konjugat

  • 24
  • 3
  • 2
  • 2
  • 1
  • 1
Dieser P4HA1 Antikörper ist unkonjugiert

Applikation

  • 26
  • 16
  • 10
  • 6
  • 3
  • 3
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Bindungsspezifität

    • 8
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    Verwendungszweck

    P4HA1 Antibody / Prolyl 4-hydroxylase subunit alpha 1

    Aufreinigung

    Immunogen affinity purified

    Immunogen

    A synthetic peptide corresponding to a sequence in the middle region of human P4HA1 was used as the immunogen for the P4HA1 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the P4HA1 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    After reconstitution, the P4HA1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    P4HA1 (Prolyl 4-Hydroxylase, alpha Polypeptide I (P4HA1))

    Andere Bezeichnung

    P4HA1

    Hintergrund

    P4HA1 antibody detects Prolyl 4-hydroxylase subunit alpha 1, an enzyme that catalyzes hydroxylation of proline residues in collagen. The UniProt recommended name is Prolyl 4-hydroxylase subunit alpha 1 (P4HA1). This enzyme is essential for collagen triple-helix stabilization, extracellular matrix formation, and connective tissue integrity.

    Functionally, P4HA1 antibody identifies a 534-amino-acid enzyme localized to the endoplasmic reticulum lumen, where it associates with prolyl 4-hydroxylase beta subunits to form the active tetrameric enzyme. P4HA1 catalyzes the post-translational modification of proline to 4-hydroxyproline, a critical step in collagen maturation that stabilizes the helical structure.

    The P4HA1 gene is located on chromosome 10q22.1 and is expressed in fibroblasts, chondrocytes, and osteoblasts. Its expression increases during wound healing, tissue remodeling, and hypoxia. P4HA1 activity is co-regulated with other collagen synthesis enzymes and is sensitive to oxygen and ascorbate availability.

    Pathologically, overexpression of P4HA1 has been linked to fibrosis, tumor progression, and hypoxia-induced extracellular matrix remodeling. Elevated P4HA1 enhances collagen deposition and stiffening of the tumor microenvironment, promoting invasion and metastasis. Conversely, inhibition of P4HA1 suppresses collagen accumulation and fibrotic scarring. Research using P4HA1 antibody aids studies in extracellular matrix biology, collagen synthesis, and disease-associated fibrosis.

    P4HA1 antibody is validated for use in western blotting, immunohistochemistry, and immunofluorescence to detect collagen-modifying enzymes. NSJ Bioreagents offers P4HA1 antibody reagents optimized for studies in connective tissue biology, tumor microenvironment, and molecular pathology.

    Structurally, Prolyl 4-hydroxylase subunit alpha 1 contains a catalytic dioxygenase domain that requires Fe2+ and ascorbate as cofactors for hydroxylation. This antibody enables characterization of P4HA1's role in collagen maturation, ECM formation, and disease progression.

    UniProt

    P13674
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