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CTSA Antikörper

Rockland 100-401-395 CTSA Reaktivität: Human WB, IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
Rockland
Produktnummer ABIN6655368
Hersteller Produkt- Nr.: 100-401-395
  • Target Alle CTSA Antikörper anzeigen
    CTSA (Cathepsin A (CTSA))
    Reaktivität
    • 53
    • 40
    • 24
    • 7
    • 6
    • 1
    • 1
    • 1
    Human
    Wirt
    • 73
    • 3
    • 1
    Kaninchen
    Klonalität
    • 74
    • 3
    Polyklonal
    Konjugat
    • 23
    • 16
    • 14
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser CTSA Antikörper ist unkonjugiert
    Applikation
    • 63
    • 30
    • 22
    • 14
    • 13
    • 13
    • 11
    • 7
    • 6
    • 5
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Hersteller Produkt- Nr.
    100-401-395
    Hersteller
    Rockland
    Verwendungszweck
    Protective Protein/Cathepsin A Antibody
    Kreuzreaktivität (Details)
    Based on sequence we expect this antibody to react with PPCA from other sources, although specific reactivity has not been confirmed.
    Aufreinigung
    This antiserum is directed against PPCA and reacts with the PPCA from human tissues.
    Sterilität
    Sterile filtered
    Immunogen
    This whole rabbit serum was prepared by repeated immunizations with native 54-kDa human Protective Protein/Cathepsin A (PPCA) precursor, purified from the medium of baculovirus infected insect cells.
    Isotyp
    IgG
    Top Product
    Discover our top product CTSA Primärantikörper
  • Applikationshinweise

    ELISA_Dilution: 1:1,000 - 1:5,000

    Immunohistochemistry_Dilution: 1:500

    Western_Blot_Dilution: 1:500 - 1:2,000

    Other: User Optimized

    Kommentare

    Suggested Applications: IP
    Anti-PPCA has been tested by immunohistochemistry and is suitable for the detection of human PPCA (54-, 32-, and 20-kDa) on Western blot, by immunoprecipitation, immunocytochemistry, and ELISA of either transfected cells (e.g. COS-1 cells) or primary cells (e.g. fibroblasts).

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: None

    Preservative: 0.1 % (w/v) Sodium Azide
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.
    Haltbarkeit
    12 months
  • Target
    CTSA (Cathepsin A (CTSA))
    Andere Bezeichnung
    Protective Protein/Cathepsin A (CTSA Produkte)
    Hintergrund

    Synonyms: rabbit anti-Protective Protein Antibody, rabbit anti-Cathepsin A Antibody, Beta Galactosidase Protective Protein antibody, Carboxypeptidase C antibody, Cathepsin A antibody, CTSA antibody, Glactosialidosis antibody, GLB2 antibody, Goldberg Syndrome antibody

    Background: Lysosomal protective protein/cathepsin A (PPCA) is a lysosomal serine carboxypeptidase that forms an intralysosomal enzyme-complex with b-galactosidase and neuraminidase (NEU1). PPCA is synthesized as a 54- kDa precursor/zymogen, and proteolytically cleaved in the lysosome into a catalytically active 32- and 20- kDa two-chain enzyme. The enzyme has cathepsin A activity at acidic pH but maintains also a deamidase/esterase activity at neutral pH . Furthermore, the human enzyme, purified from platelets and lymphocytes, has been shown to function on the inactivation of selected neuropeptides, like substance P, oxytocin, and endothelin I. The autosomal recessive genetic deficiency of PPCA causes galactosialidosis, a neurodegenerative lysosomal storage disorder, resulting in the secondary deficiencies of b-galactosidase and NEU1.

    Gene Name: CTSA, PPGB

    Gen-ID
    5476
    UniProt
    P10619
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