Thermo Fisher Scientific KCNT1 Monoclonal Antibody (N3/26)
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Applications
Tested Dilution
Publications
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
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) if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
KCNT1,
uniProtId:
Q9Z258-1,
ncbiNodeId:
10114,
antigenRange:
1168-1237,
antigenLength:
1237,
antigenImageFileName:
MA5-27609_KCNT1_Q9Z258-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-27609_KCNT1_Q9Z258-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
View additional formats
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
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 140kDa. Weak human detection.approximately 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 which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, 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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