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バルクの問い合わせ
由来生物
rabbit
品質水準
結合体
unconjugated
抗体製品の状態
affinity isolated antibody
抗体製品タイプ
primary antibodies
クローン
polyclonal
フォーム
buffered aqueous solution
交差性
bovine, human, mouse
テクニック
western blot: 0.4 μg/mL using mouse neuronal cell lysate and human retinal extracts
UniProtアクセッション番号
輸送温度
dry ice
保管温度
−20°C
ターゲットの翻訳後修飾
unmodified
遺伝子情報
human ... KIF5A(3798)
mouse ... Kif5a(16572)
詳細
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.
アプリケーション
Anti-Kinesin 5A antibody produced in rabbit has been used in immunofluorescence and immunohistochemistry[1].
生物化学的／生理学的作用
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.
物理的形状
PBS溶液 (1mg/mL BSA, 0.05%アジ化ナトリウム含有)。
免責事項
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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保管分類コード
10 - Combustible liquids
WGK
nwg
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
K0889-VAR:
K0889-BULK:
K0889-100UG:
K0889-100UG-PW:
Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.
Xia CH
The Journal of Cell Biology, 161, 55-66 (2003)
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
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
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
アクティブなフィルタ
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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