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Thermo Fisher Scientific ATP7B Monoclonal Antibody (L62/29), PerCP
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Thermo Fisher Scientific ATP7B Monoclonal Antibody (L62/29), PerCP

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ATP7B 단백질을 인식하는 마우스 단클론 항체로, PerCP로 표지되어 있습니다. Western blot, IHC, ICC, IP 등 다양한 응용에 사용 가능하며 인간, 마우스, 랫트 시료에 반응합니다. 단백질 G로 정제되었으며 4°C에서 보관합니다.

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마지막 업데이트 2025. 08. 01. 오후 06:29
Thermo Fisher Scientific MA545524 ATP7B Monoclonal Antibody (L62/29), PerCP 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific ATP7B Monoclonal Antibody (L62/29), PerCP

Applications and Tested Dilutions

Application Tested Dilution Notes
Western Blot (WB) 1:1,000
Immunohistochemistry (IHC) Assay-dependent
Immunocytochemistry (ICC/IF) 1:100
Immunoprecipitation (IP) Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone L62/29
Immunogen Synthetic peptide amino acids 3–21 (cytoplasmic N-terminus) of human Copper-transporting ATPase2
Conjugate PerCP
Excitation / Emission Max 482 / 675 nm
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer 95.64 mM phosphate / 2.48 mM MES, pH 7.4, with 0.5 M EDTA
Contains No preservative
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2931978

Available Formats

Product Specific Information

  • 1 µg/mL of MA5-45524 was sufficient for detection of Copper-transporting ATPase2 in 20 µg of rat brain lysate by colorimetric immunoblot analysis using Goat IgG:HRP as the secondary antibody.
  • Detects approximately 160 kDa in rat brain membrane preparations.
  • This antibody was formerly sold as clone S62-29.

Target Information

The ATP7B gene encodes a member of the P-type cation transport ATPase family. The protein contains multiple membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least two putative copper-binding sites. It functions as a monomer, exporting copper out of cells, such as the efflux of hepatic copper into bile. Alternate splice variants with distinct cellular localizations have been characterized. Mutations in this gene are associated with Wilson disease (WD).


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

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