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Thermo Fisher Scientific Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme) Monoclonal Antibody (SOD1, 3924)
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Thermo Fisher Scientific Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme) Monoclonal Antibody (SOD1, 3924)

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Human SOD1 단백질을 표적으로 하는 Mouse monoclonal antibody로, Western blot 및 IHC(P) 등 다양한 응용에 적합. Recombinant fragment(aa14-148)를 면역원으로 사용. 200 µg/mL 농도의 액상 형태로 제공되며, 4°C 보관.

카탈로그번호
6647-MSM4-P0
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 10:17
Thermo Fisher Scientific 6647-MSM4-P0 Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme) Monoclonal Antibody (SOD1, 3924) 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, 3924)

Applications

Application Tested Dilution Publications
Western Blot (WB) 2–4 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, 3924
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 min 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 min at 95°C followed by cooling at room temperature for 20 min.


Target Information

SOD1 (Superoxide Dismutase 1) 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, acting as a homodimer to convert harmful superoxide radicals to 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.
Rare transcript variants have been reported for this gene.


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

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