
Thermo Fisher Scientific Syntrophin alpha-1 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
1-3 µg/mL
View 1 publication 1 publication
Product Specifications
Species Reactivity
Human, Mouse, Rat
Published species
Mouse
Host/Isotype
Goat / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Synthetic peptide corresponding to the N terminus amino acids ASGRRAPRTGLLE (aa 2-14). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Syntrophin alpha-1,
uniProtId:
Q13424-1,
ncbiNodeId:
9606,
antigenRange:
2-14,
antigenLength:
505,
antigenImageFileName:
PA1-9107_Syntrophin_alpha-1_Q13424-1_Goat.svg,
antigenImageFileNamePDP:
PA1-9107_Syntrophin_alpha-1_Q13424-1_Goat_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 mg/mL
Purification
Ammonium sulfate precipitation
Storage buffer
TBS, pH 7.3, with 0.5% BSA
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Wet ice
RRID
AB_2191795
Product Specific Information
This antibody is predicted to react with bovine, canine and porcine based on sequence homology.
This antibody is tested in Peptide ELISA: antibody detection limit dilution 32,000.
Target Information
Syntrophin alpha-1 (Dystrophin, SNTA1) is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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