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HSPG2 Antikörper (AA 3601-3700)

HSPG2 Reaktivität: Human ELISA, IHC (p), FACS, IHC (fro), IF (cc), IF (p) Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN709256
  • Target Alle HSPG2 Antikörper anzeigen
    HSPG2 (Heparan Sulfate Proteoglycan 2 (HSPG2))
    Bindungsspezifität
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 3601-3700
    Reaktivität
    • 27
    • 18
    • 7
    • 4
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    Human
    Wirt
    • 18
    • 6
    • 6
    Kaninchen
    Klonalität
    • 19
    • 11
    Polyklonal
    Konjugat
    • 20
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser HSPG2 Antikörper ist unkonjugiert
    Applikation
    • 19
    • 13
    • 9
    • 8
    • 7
    • 6
    • 5
    • 4
    • 4
    • 3
    • 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))
    Kreuzreaktivität
    Human
    Homologie
    Mouse,Rat,Cow,Pig,Horse
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human Heparan Sulfate Proteoglycan 2
    Isotyp
    IgG
    Top Product
    Discover our top product HSPG2 Primärantikörper
  • Applikationshinweise
    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
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Haltbarkeit
    12 months
  • Target
    HSPG2 (Heparan Sulfate Proteoglycan 2 (HSPG2))
    Andere Bezeichnung
    Heparan Sulfate Proteoglycan 2 (HSPG2 Produkte)
    Synonyme
    HSPG antikoerper, PLC antikoerper, PRCAN antikoerper, SJA antikoerper, SJS antikoerper, SJS1 antikoerper, HSPG2 antikoerper, AI852380 antikoerper, Pcn antikoerper, Plc antikoerper, per antikoerper, Per antikoerper, heparan sulfate proteoglycan 2 antikoerper, perlecan (heparan sulfate proteoglycan 2) antikoerper, HSPG2 antikoerper, hspg2 antikoerper, Hspg2 antikoerper
    Hintergrund

    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].

    Gen-ID
    117194
    Pathways
    Glycosaminoglycan Metabolic Process, Lipid Metabolism
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