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Thermo Fisher Scientific Arginase 1 (ARG1) Monoclonal Antibody (OTI4D7)
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Thermo Fisher Scientific Arginase 1 (ARG1) Monoclonal Antibody (OTI4D7)

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인간 Arginase 1 단백질을 인식하는 Mouse monoclonal 항체. Western blot에 최적화된 1:500 희석 비율. Affinity chromatography로 정제된 액상 포맷. 세포 내 Arginase 1 발현 연구에 적합. 연구용으로만 사용 가능.

카탈로그번호
TA813196
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 04:35
Thermo Fisher Scientific TA813196 Arginase 1 (ARG1) Monoclonal Antibody (OTI4D7) 100 ul pk판매 단위 pk ·
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676,500원VAT 포함 744,150원

Thermo Fisher Scientific · Thermo Fisher Scientific Arginase 1 (ARG1) Monoclonal Antibody (OTI4D7)

Applications

Western Blot (WB)

  • Tested Dilution: 1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI4D7
Immunogen Full length human recombinant protein of human ARG1 (NP_000036) produced in HEK293T cell
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage buffer PBS with 50% glycerol, 1% BSA
Contains 0.02% sodium azide
Storage conditions -20°C
Shipping conditions Ambient (domestic); Wet ice (international)

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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