
Thermo Fisher Scientific KCNQ1 Monoclonal Antibody (N37A/10), PerCP
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Applications
Tested Dilution
Publications
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
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 if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
KCNQ1,
uniProtId:
P51787-1,
ncbiNodeId:
9606,
antigenRange:
2-101,
antigenLength:
676,
antigenImageFileName:
MA5-45409_KCNQ1_P51787-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-45409_KCNQ1_P51787-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
PerCP PerCP PerCP
View additional formats
Excitation/Emission Max
482/675 nm View spectra
Form
Liquid
Concentration
1 mg/mL
Purification
Protein G
Storage buffer
95.64mM phosphate/2.48mM MES, pH 7.4, with 0.5M EDTA
Contains
no preservative
Storage conditions
4° C
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2931863
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 75kDa.
Target Information
Voltage-gated K+ channels in the plasma membrane control the repolarization and the frequency of action potentials in neurons, muscles and other excitable cells. A specific K+ channel, comprised of an alpha subunit KCNQ1 and a beta subunit KCNE1, a small protein which spans the membrane only once, is predominantly expressed in the heart and in the cochlea, and is responsible for regulating the slow, depolarization-activated potassium current. Mutations in the genes encoding for KCNQ1 and KCNE1 lead to cardiac disease because they directly impair electrical signaling, and mutations in KCNQ4 are implicated in the onset of deafness. KCNQ proteins, including KCNQ1 and KCNQ4, characteristically contain six transmembrane domains and function as tetramers. KCNQ4 forms heteromeric channels with KCNQ3 and is expressed in several tissues, including the cochlea, where it is present in outer hair cells.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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