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Thermo Fisher Scientific Placental Alkaline Phosphatase Polyclonal Antibody
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Thermo Fisher Scientific Placental Alkaline Phosphatase Polyclonal Antibody

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인체 PLAP에 특이적인 Rabbit Polyclonal Antibody로 Western blot, IHC, ICC/IF에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보존. 염증성 질환 및 생식세포 종양 연구에 유용.

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마지막 업데이트 2025. 08. 05. 오전 08:37
Thermo Fisher Scientific PA583438 Placental Alkaline Phosphatase Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
740,000원VAT 포함 814,000원

Thermo Fisher Scientific · Thermo Fisher Scientific Placental Alkaline Phosphatase Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:500–1:1,000
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human ALPP. Recombinant protein control fragment (Product #RP-98831).
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2790593

Product Specific Information

Immunogen sequence:
NWYSDADVPA SARQEGCQDI ATQLISNMDI

Target Information

Placental Alkaline Phosphatase (PLAP) plays a role in regulating specific inflammatory disease processes. There are four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney types. PLAP reacts with a membrane-bound isoenzyme (Regan and Nagao type) occurring in the placenta during the third trimester of gestation. It is useful in identifying testicular germ cell tumors. PLAP-positive somatic cell tumors uniformly express epithelial membrane antigen (EMA). A proposed function of PLAP is matrix mineralization; however, mice lacking functional PLAP show normal skeletal development. PLAP has been linked to hypophosphatasia, a disorder characterized by hypercalcemia and skeletal defects. The severity and onset depend on the specific mutation.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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