Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Peroxidasin antibody

PXDN Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7269230
  • Target See all Peroxidasin (PXDN) Antibodies
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Reactivity
    • 13
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 10
    • 3
    Rabbit
    Clonality
    • 11
    • 2
    Polyclonal
    Conjugate
    • 8
    • 4
    • 1
    This Peroxidasin antibody is un-conjugated
    Application
    • 13
    • 4
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purpose
    PXDN Rabbit pAb
    Cross-Reactivity
    Human, Mouse
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human PXDN.
    Isotype
    IgG
    Top Product
    Discover our top product PXDN Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
    Alternative Name
    PXDN (PXDN Products)
    Synonyms
    D2S448 antibody, D2S448E antibody, MG50 antibody, PRG2 antibody, PXN antibody, VPO antibody, 2310075M15Rik antibody, C85409 antibody, E330004E07 antibody, VPO1 antibody, mKIAA0230 antibody, peroxidasin antibody, PXDN antibody, Pxdn antibody
    Background
    This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis.,PXN,VPO,MG50,PRG2,ASGD7,COPOA,D2S448,D2S448E,PXDN,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,PXDN
    Gene ID
    7837
    UniProt
    Q92626
You are here:
Support