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Antikörper
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anti-Placental Alkaline Phosphatase (PLAP) Antikörper
Placental Alkaline Phosphatase (PLAP) Antikörper
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| Synonyme |
DOA1, PLAP, PLA2P, FLJ11281, FLJ12699, cb623, zgc:56568, zgc:66193, wu:fc45d08, wu:fi33e06, PLAA |
| Klonalität |
Monoklonal (SP15) |
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Wirt
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Reaktivität
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Applikation
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| Produktnummer |
ABIN125301 |
| Menge |
6ml (1 to 4 ug/ml) (Varianten) |
| Preis |
231.00 $ Zzgl. Versandkosten $35.00
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| Lieferung nach |
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| Verfügbarkeit |
Lieferung in 5 Werktagen |
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Immunogen
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Recombinant protein encoding human Placental Alkaline Phosphatase (PLAP).
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Format
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Supernatant (prediluted)
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Isotyp
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IgG (Passende Sekundärantikörper)
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Klon
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SP15
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Spezifität
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This antibody reacts with a membrane-bound isoenzyme (Regan and Nagao type) of Placental Alkaline Phosphatase (PLAP) occurring in the placenta during the 3rd trimester of gestation. This antibody is highly specific to PLAP and shows no cross-reaction with other isoenzymes of alkaline phosphatases. It is useful in the identification of testicular germ cell tumors. Unlike germ cell tumors, PLAP-positive somatic cell tumors uniformly express epithelial membrane antigen (EMA).This antibody crossreacts with Human, Mouse and Rat.
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Applikationshinweise
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Staining Protocol: We suggest an incubation period of 30 minutes at room temperature. However, depending upon the fixation conditions and the staining system employed, optimal incubation should be determined by the user. Formalin fixed paraffin embedded tissue sections require high temperature antigen unmasking with 10 mM citrate buffer, pH 6.0 prior to immunostaining. Positive Control: Placenta. Cellular localization: Cytoplasmic
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Konzentration
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1 to 4 ug/ml
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Buffer
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This antibody has been pretitered and quality controlled to work on formalin-fixed paraffin-embedded as well as acetone fixed cryostat tissue sections. No further titration is required.
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Lagerung
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Store the antibody at 2-8o c. Do not use it beyond the expiration date stated on the label.
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Forschungsgebiet
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Enzyme
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Beschränkungen
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Für Forschungszwecke. Als CE-zertifizierter Antikörper in der Europäischen Union für In Vitro Diagnostik (IVD) zugelassen.
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