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HSPG2 anticorps (AA 3601-3700)

HSPG2 Reactivité: Humain ELISA, IHC (p), FACS, IHC (fro), IF (cc), IF (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN709256
  • Antigène Voir toutes HSPG2 Anticorps
    HSPG2 (Heparan Sulfate Proteoglycan 2 (HSPG2))
    Épitope
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 3601-3700
    Reactivité
    • 27
    • 18
    • 9
    • 4
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 18
    • 8
    • 6
    Lapin
    Clonalité
    • 19
    • 13
    Polyclonal
    Conjugué
    • 22
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp HSPG2 est non-conjugé
    Application
    • 20
    • 15
    • 11
    • 10
    • 7
    • 6
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
     Réactivité croisée
    Humain
    Homologie
    Mouse,Rat,Cow,Pig,Horse
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human Heparan Sulfate Proteoglycan 2
    Isotype
    IgG
    Top Product
    Discover our top product HSPG2 Anticorps primaire
  • Indications d'application
    ELISA 1:500-1000
    FCM 1:20-100
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • Antigène
    HSPG2 (Heparan Sulfate Proteoglycan 2 (HSPG2))
    Autre désignation
    Heparan Sulfate Proteoglycan 2 (HSPG2 Produits)
    Synonymes
    anticorps HSPG, anticorps PLC, anticorps PRCAN, anticorps SJA, anticorps SJS, anticorps SJS1, anticorps HSPG2, anticorps AI852380, anticorps Pcn, anticorps Plc, anticorps per, anticorps Per, anticorps heparan sulfate proteoglycan 2, anticorps perlecan (heparan sulfate proteoglycan 2), anticorps HSPG2, anticorps hspg2, anticorps Hspg2
    Sujet

    Synonyms: Perlecan, Basement membrane specic heparan sulfate proteoglycan core protein, Endorepellin domain V region, Heparan Sulfate Proteoglycan, Heparan sulfate proteoglycan of basement membrane, HSPG 2, HSPG, Hspg2, LG3 peptide, Perlecan, PLC antibody Schwartz Jampel syndrome 1 chondrodystrophic myotonia, SJA antibody SJS antibody SJS1 antibody.

    Background: This gene encodes the perlecan protein, which consists of a core protein to which three long chains of glycosaminoglycans(heparan sulfate or chondroitin sulfate) are attached. The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules. It has been shown that this protein interacts with laminin, prolargin, collagen type IV, FGFBP1, FBLN2, FGF7 and Transthyretin, etc. and plays essential roles in multiple biological activities. Perlecan is a key component of the vascular extracellular matrix, where it helps to maintain the endothelial barrier function. It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis. It can also promote growth factor (e.g., FGF2) activity and thus stimulate endothelial growth and re-generation. It is a major component of basement membranes, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion. Mutations in this gene cause Schwartz-Jampel syndrome type 1, Silverman-Handmaker type of dyssegmental dysplasia, and Tardive dyskinesia.[provided by RefSeq, Mar 2010].

    ID gène
    117194
    Pathways
    Glycosaminoglycan Metabolic Process, Lipid Metabolism
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