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Thermo Fisher Scientific KCNQ1 Monoclonal Antibody (N37A/10), PerCP
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Thermo Fisher Scientific KCNQ1 Monoclonal Antibody (N37A/10), PerCP

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KCNQ1 단백질을 인식하는 Mouse monoclonal antibody (Clone N37A/10)로 PerCP 형광 표지. WB, IHC, ICC, IP 등 다양한 응용에 사용 가능. Human, Mouse, Rat, Hamster 반응성. Protein G 정제, 1 mg/mL 농도, 4°C 보관.

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마지막 업데이트 2025. 08. 04. 오전 03:34
Thermo Fisher Scientific MA545409 KCNQ1 Monoclonal Antibody (N37A/10), PerCP 100 ug pk판매 단위 pk ·
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663,800원VAT 포함 730,180원

Thermo Fisher Scientific · Thermo Fisher Scientific KCNQ1 Monoclonal Antibody (N37A/10), PerCP

Applications and Tested Dilutions

Application Tested Dilution Notes
Western Blot (WB) 1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:1,000
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1:1,000
Immunocytochemistry (ICC/IF) 1:100
Immunoprecipitation (IP) Assay-dependent
Antibody Microarray (AM) Assay-dependent

Product Specifications

Specification Detail
Species Reactivity Hamster, Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone N37A/10
Immunogen Fusion protein amino acids 2–101 of human KCNQ1
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_2931863

Available Formats

Product Specific Information

1 µg/mL of MA5-45409 was sufficient for detection of KCNQ1 in 10 µg of COS-1 cell lysate transiently expressing KCNQ1 by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody. Detects approximately 75 kDa.

Target Information

Voltage-gated K⁺ channels in the plasma membrane control the repolarization and frequency of action potentials in neurons, muscles, and other excitable cells.
The KCNQ1 alpha subunit and KCNE1 beta subunit form a specific K⁺ channel predominantly expressed in the heart and cochlea, regulating the slow, depolarization-activated potassium current.
Mutations in KCNQ1 and KCNE1 cause cardiac disease due to impaired electrical signaling, while KCNQ4 mutations are linked to deafness.
KCNQ proteins have six transmembrane domains and function as tetramers; KCNQ4 forms heteromeric channels with KCNQ3 and is expressed in tissues including the cochlea.


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

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