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Thermo Fisher Scientific Arginase 1 Polyclonal Antibody
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Thermo Fisher Scientific Arginase 1 Polyclonal Antibody

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Thermo Fisher Scientific의 Arginase 1 Polyclonal Antibody는 소 간에서 유래한 Arginase를 인식하는 토끼 IgG 항체입니다. Western blot 및 Immunomicroscopy에 사용 가능하며, 세포 내 Arginase-1 발현 연구에 적합합니다. 액상 형태로 제공되며 4°C 또는 -20°C에서 안정적으로 보관할 수 있습니다.

카탈로그번호
PA126408
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 07:57
Thermo Fisher Scientific PA126408 Arginase 1 Polyclonal Antibody 1 mg pk판매 단위 pk ·
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805,000원VAT 포함 885,500원

Thermo Fisher Scientific · Thermo Fisher Scientific Arginase 1 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: Assay-dependent

Immunomicroscopy (IM)

  • Tested Dilution: Assay-dependent

Product Specifications

항목 내용
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Arginase from bovine liver
Conjugate Unconjugated
Form Liquid
Concentration 10 mg/mL
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_2289843

Product Specific Information

PA1-26408 detects liver Arginase from bovine samples.


Target Information

Arginase-1 (Arg1) is a 35 kDa enzyme converting L-arginine to urea and L-ornithine, which is the final step in the urea cycle. The resulting polyamines are important for cell proliferation and removal of toxins that arise from protein degradation. By degrading arginine, Arginase 1 deprives NO synthase of its substrate and down-regulates nitric oxide production.

In both human and mouse, Arginase 1 is expressed in the liver, neutrophils, myeloid derived suppressor cells (MDSC), and neural stem cells. In human, expression in blood neutrophils but not in CCR3+ granulocytes has been reported. In mice, expression of Arginase 1 is one of the hallmarks of alternatively activated macrophages (M2a). Arginase-1 may be expressed in the myeloid cells infiltrating tumors and is typically found in the majority of hepatocellular carcinomas. Defects in Arginase 1 are the cause of argininemia, an autosomal recessive disorder characterized by hyperammonemia.


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

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