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Thermo Fisher Scientific Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme) Monoclonal Antibody (SOD1, 4330)
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Thermo Fisher Scientific Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme) Monoclonal Antibody (SOD1, 4330)

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SOD1 단백질을 인식하는 마우스 모노클로날 항체로, Western blot과 IHC(P) 등 다양한 응용 가능. Human SOD1에 반응하며 단백질 정제는 Protein A/G 방식. PBS 완충액에 보관되며, 항산화 효소 연구에 적합.

카탈로그번호
6647-MSM10-P0
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 11:31
Thermo Fisher Scientific 6647-MSM10-P0 Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme) Monoclonal Antibody (SOD1, 4330) 20 ug pk판매 단위 pk ·
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441,900원VAT 포함 486,090원

Thermo Fisher Scientific · Thermo Fisher Scientific Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme) Monoclonal Antibody (SOD1, 4330)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1–2 µg/mL
Peptide Array (Array) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone SOD1, 4330
Immunogen Recombinant fragment (around aa14–148) of human SOD1
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Immunohistochemistry (PFA fixed): incubate antibody for 30 minutes at room temperature.
  • Staining of formalin-fixed tissues requires heating tissue sections in 10 mM Tris with 1 mM EDTA (pH 9.0) for 45 minutes at 95°C, followed by cooling at room temperature for 20 minutes.

Target Information

SOD1 (superoxide dismutase) binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. This isozyme is a soluble cytoplasmic protein that acts as a homodimer to convert harmful superoxide radicals into molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis (ALS). Rare transcript variants have also been reported.


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

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