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Thermo Fisher Scientific Arginase 1 Monoclonal Antibody (A1exF5), Brilliant Violet 650, eBioscience
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Thermo Fisher Scientific Arginase 1 Monoclonal Antibody (A1exF5), Brilliant Violet 650, eBioscience

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인간 및 마우스 Arginase 1을 인식하는 단클론 항체로, Brilliant Violet 650 형광체로 표지되어 있습니다. 유세포분석용으로 검증되었으며, 세포 내 염색에 적합합니다. 4°C 암소 보관, 동결 금지. 연구용으로만 사용 가능합니다.

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416-3697-8x (2개 옵션)
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마지막 업데이트 2025. 08. 04. 오후 04:52
Thermo Fisher Scientific 416-3697-82 Arginase 1 Monoclonal Antibody (A1exF5), Brilliant Violet 650, eBioscience 100 ug pk판매 단위 pk ·
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614,900원VAT 포함 676,390원
Thermo Fisher Scientific 416-3697-80 Arginase 1 Monoclonal Antibody (A1exF5), Brilliant Violet 650, eBioscience 25 ug pk판매 단위 pk ·
재고 확인 필요
286,500원VAT 포함 315,150원

Thermo Fisher Scientific · Thermo Fisher Scientific Arginase 1 Monoclonal Antibody (A1exF5), Brilliant Violet 650, eBioscience

Applications and Tested Dilution

Application Tested Dilution
Flow Cytometry (Flow) 1.0 µg/test

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rat / IgG2a, kappa
Recommended Isotype Control Rat IgG2a kappa Isotype Control (eBR2a), Brilliant Violet™ 650, eBioscience™
Class Monoclonal
Type Antibody
Clone A1exF5
Immunogen E.coli-derived recombinant mouse Arginase 1
Conjugate Brilliant Violet™ 650
Excitation / Emission Max 407 / 646 nm
Form Liquid
Concentration 0.2 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.2, with BSA
Contains 0.09% sodium azide
Storage Conditions 4°C, store in dark, DO NOT FREEZE
Shipping Conditions Wet ice
RRID AB_3074122

Available Conjugate Formats

  • Alexa Fluor 488
  • Alexa Fluor 700
  • APC
  • Brilliant UV 805
  • Brilliant Violet 421
  • Brilliant Violet 480
  • Brilliant Violet 711
  • eFluor 450
  • PE
  • PE-Cyanine7
  • PerCP-eFluor 710
  • Request custom conjugation

Product Specific Information

The monoclonal antibody A1exF5 recognizes both human and mouse Arginase 1 (Arg1), a cytosolic enzyme.
This clone is compatible with standard intracellular staining protocols and the Foxp3/Transcription Factor Staining Buffer Set.

Applications Reported:
Intracellular staining followed by flow cytometric analysis.

Applications Tested:
Tested by intracellular staining of normal human lysed whole blood cells using the Intracellular Fixation & Permeabilization Buffer Set (Product # 88-8824-00).
Recommended ≤1.0 µg per test (100 µL final volume). Adjust cell number empirically (10⁵–10⁸ cells/test).
Optimize antibody titration for best performance.

Fluorochrome Information:
Brilliant Violet™ 650 (BV650) emits at 649 nm and is excited by a 405 nm violet laser. Ensure cytometer compatibility.

Staining Buffer Recommendations:
When using multiple polymer dye-conjugated antibodies, use Super Bright Complete Staining Buffer (#SB-4401-42) or Brilliant Stain Buffer™ (#00-4409-75) to minimize non-specific interactions.

Light Sensitivity:
Protect from light due to photo-induced oxidation sensitivity.

Fixation:
Samples can be stored up to 3 days at 4°C in the dark using IC Fixation Buffer (#00-8222-49) or 1-Step Fix/Lyse Solution (#00-5333-54).
BV650 is not compatible with methanol-based fixation.

Excitation / Emission: 407 nm / 649 nm
Laser: Violet Laser

BRILLIANT VIOLET™ is a trademark of Becton, Dickinson and Company or its affiliates, used under license. Powered by Sirigen™.


Target Information

Arginase-1 (Arg1) is a 35 kDa enzyme that converts L-arginine into urea and L-ornithine, the final step in the urea cycle.
The resulting polyamines support cell proliferation and detoxification.
Arginase 1 modulates nitric oxide production by depleting L-arginine, the substrate for NO synthase.

In both human and mouse, Arginase 1 is expressed in:

  • Liver
  • Neutrophils
  • Myeloid-derived suppressor cells (MDSCs)
  • Neural stem cells

Human expression is observed in blood neutrophils (not in CCR3⁺ granulocytes).
In mice, Arginase 1 is a hallmark of alternatively activated macrophages (M2a).
It may also be expressed in tumor-infiltrating myeloid cells and hepatocellular carcinomas.
Defects in Arginase 1 cause argininemia, an autosomal recessive disorder characterized by hyperammonemia.


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


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