生物来源
rabbit
质量水平
偶联物
unconjugated
抗体形式
affinity isolated antibody
抗体产品类型
primary antibodies
克隆
polyclonal
表单
buffered aqueous solution
种属反应性
bovine, human, mouse
技术
western blot: 0.4 μg/mL using mouse neuronal cell lysate and human retinal extracts
UniProt登记号
运输
dry ice
储存温度
−20°C
靶向翻译后修饰
unmodified
基因信息
human ... KIF5A(3798)
mouse ... Kif5a(16572)
一般描述
The gene KIF5A (kinesin family member 5A) is mapped to human chromosome 12. The encoded kinesin is expressed in all neurons, and present in neuronal cytoplasm, which includes the cell body, dendrites, and axon.
免疫原
synthetic peptide corresponding to amino acid residues 1007-1027 from mouse kinesin 5A.
应用
Anti-Kinesin 5A antibody produced in rabbit has been used in immunofluorescence and immunohistochemistry.
生化/生理作用
The gene KIF5A (kinesin family member 5A) encodes a kinesin heavy chain that may be involved in the microtubule-dependent slow axonal transport of neurofilament proteins.
Mutations in this gene have been associated with hereditary spastic paraplegia.
Mutations in this gene have been associated with hereditary spastic paraplegia.
外形
Solution in phosphate buffered saline containing 1 mg/mL BSA and 0.05% sodium azide.
免责声明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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储存分类代码
10 - Combustible liquids
WGK
nwg
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.
Xia CH
The Journal of Cell Biology, 161, 55-66 (2003)
Ping Shi et al.
Biochimica et biophysica acta, 1802(9), 707-716 (2010-06-01)
Transport of material and signals between extensive neuronal processes and the cell body is essential to neuronal physiology and survival. Slowing of axonal transport has been shown to occur before the onset of symptoms in amyotrophic lateral sclerosis (ALS). We
Evan Reid et al.
American journal of human genetics, 71(5), 1189-1194 (2002-10-02)
We have identified a missense mutation in the motor domain of the neuronal kinesin heavy chain gene KIF5A, in a family with hereditary spastic paraplegia. The mutation occurs in the family in which the SPG10 locus was originally identified, at
Ingo Spitzbarth et al.
Brain and behavior, 6(7), e00472-e00472 (2016-06-02)
CDV-DL (Canine distemper virus-induced demyelinating leukoencephalitis) represents a spontaneously occurring animal model for demyelinating disorders. Axonopathy represents a key pathomechanism in this disease; however, its underlying pathogenesis has not been addressed in detail so far. This study aimed at the
S Schwarz et al.
Scientific reports, 10(1), 5380-5380 (2020-03-28)
Dogs share many chronic morbidities with humans and thus represent a powerful model for translational research. In comparison to rodents, the canine ganglioside metabolism more closely resembles the human one. Gangliosides are components of the cell plasma membrane playing a
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