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Thermo Fisher Scientific ALPP Monoclonal Antibody (OTI1H2), TrueMAB
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Thermo Fisher Scientific ALPP Monoclonal Antibody (OTI1H2), TrueMAB

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인간 ALPP 단백질을 인식하는 마우스 단클론 항체로 Western blot에 적합합니다. 동결건조 형태이며 PBS 완충액에 trehalose 포함. 연구용으로 사용되며, 재구성 및 결합 실험에 적합한 고순도 항체입니다.

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마지막 업데이트 2025. 08. 05. 오전 04:45
Thermo Fisher Scientific CF506374 ALPP Monoclonal Antibody (OTI1H2), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific ALPP Monoclonal Antibody (OTI1H2), TrueMAB

Applications

  • Western Blot (WB)

Tested Dilution

  • 1:200–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone OTI1H2
Immunogen Full length human recombinant protein of human ALPP produced in HEK293T cell
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).

Target Information

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

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

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