
Thermo Fisher Scientific Kinesin 5A Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
0.5-2 µg/mL
View 4 publications 4 publications
Immunocytochemistry (ICC/IF)
1-2 µg/mL
Immunoprecipitation (IP)
-
View 1 publication 1 publication
Product Specifications
Species Reactivity
Bovine, Human, Mouse
Published species
Human, Mouse
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Synthetic Peptide: C(1007) G Y E A E D Q A K L F P L H Q E T A A S(1027) if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Kinesin 5A,
uniProtId:
P33175-1,
ncbiNodeId:
10090,
antigenRange:
1007-1027,
antigenLength:
1027,
antigenImageFileName:
PA1-642_Kinesin_5A_P33175-1_Rabbit.svg,
antigenImageFileNamePDP:
PA1-642_Kinesin_5A_P33175-1_Rabbit_PDP.jpeg,
sortOrder:
2}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS with 1mg/mL BSA
Contains
0.05% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2132216
Product Specific Information
PA1-642 detects kinesin 5A from mouse, human, and bovine samples. This antibody is specific for kinesin 5A and does not detect other kinesin isotypes.
PA1-642 has been successfully used in Western blot procedures. By Western blot, this antibody detects an ~110 kDa protein representing kinesin 5A from mouse neuronal cell lysate and human retinal extracts.
The PA1-642 immunizing peptide corresponds to amino acid residues 1007-1027 from mouse kinesin 5A. This sequence is completely conserved in human. This peptide (Cat. # PEP-197) is available for use in neutralization and control experiments.
Target Information
This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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