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Thermo Fisher Scientific KCNT1 Monoclonal Antibody (N3/26)
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Thermo Fisher Scientific KCNT1 Monoclonal Antibody (N3/26)

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KCNT1 단백질을 인식하는 Mouse IgG1 단일클론 항체로, Human/Mouse/Rat 시료에 반응합니다. WB, IHC, ICC 등 다양한 분석에 적합하며, 단백질 G 정제 및 액상 형태로 제공됩니다. -20°C 보관, 연구용 전용 제품입니다.

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마지막 업데이트 2025. 08. 04. 오후 04:05
Thermo Fisher Scientific MA527609 KCNT1 Monoclonal Antibody (N3/26) 100 ug pk판매 단위 pk ·
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775,200원VAT 포함 852,720원

Thermo Fisher Scientific · Thermo Fisher Scientific KCNT1 Monoclonal Antibody (N3/26)

Thermo Fisher Scientific KCNT1 Monoclonal Antibody (N3/26)

Applications and Tested Dilutions

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

Product Specifications

Property Description
Species Reactivity Human, Mouse, Rat
Host/Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone N3/26
Immunogen Fusion protein amino acids 1168–1237 of rat Slo2.2 (Slack)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.09% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2735247

Available Conjugated Formats

Product Specific Information

1 µg/mL of MA5-27609 was sufficient for detection of Slo2.2 in 10 µg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody. Detects approximately 140 kDa. Weak human detection. Does not cross-react with KCNT2/Slo2.1/Slick.

Target Information

Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume.
This gene encodes a sodium-activated potassium channel subunit thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause early-onset epileptic disorders such as malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy.
Alternative splicing results in multiple transcript variants.

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

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