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The protein encoded by KIF1A is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. 再加上，我们可以发KIF1A 试剂盒 (5) 和 KIF1A 蛋白 (1)和数多这个蛋白质的别的产品。
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Mouse (Murine) Monoclonal KIF1A Primary Antibody for IF, WB - ABIN968736
Bloom: The UNC-104/KIF1 family of kinesins. in Current opinion in cell biology 2001
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these findings support a primary role for KIF1A in the anterograde transport of BACE1 (显示 BACE 抗体).
propose that KIF1A is essential for the survival and function of sensory neurons.
The Doublecortin (显示 DCX 抗体) specifically enhances binding of the ADP-bound Kif1a motor domain to microtubules. Dcx (显示 DCX 抗体) is essential for the function of Kif1a, a kinesin-3 motor protein (显示 MYO7A 抗体) that traffics synaptic vesicles.
This study demonstrated that KIF1A is indispensable for BDNF (显示 BDNF 抗体)-mediated hippocampal synaptogenesis and learning enhancement induced by enrichment.
The KIF1A-microtubule binding free energy is dominated by van (显示 SLC11A2 抗体) der (显示 GDF3 抗体) Waals interactions and electrostatic interactions.
crystal structures of monomeric KIF1A with three transition-state analogs; structures show that KIF1A uses two microtubule-binding loops in an alternating manner to change its interaction with microtubules during the ATP hydrolysis cycle
propose a model mechanism for microtubule activation of Mg-ADP release from KIF1A
We report a child with a de novo KIF1A gene mutation who was found to have bilateral optic nerve hypoplasia and atrophy.
BORC and Arl8 (显示 ARL5B 抗体) function upstream of two structurally distinct kinesin types: kinesin-1 (KIF5B (显示 KIF5B 抗体)) and kinesin-3 (KIF1Bbeta and KIF1A).
De novo missense variant affecting the motor domain of KIF1A was identified as a cause of PEHO syndrome.
Mutations outside the motor domain of the gene can cause (recessive) SPG30 and extends the genotype-phenotype association for KIF1A-related diseases.
This study further delineates clinical features of de novo KIF1A mutations
KIF1A variants in dominant and sporadic forms of hereditary spastic paraparesis.
KIF1A should be considered a candidate gene for hereditary paraplegias regardless of inheritance pattern.
Findings provide evidence that de novo missense mutations in the motor domain of KIF1A cause a more severe phenotype that overlaps with that associated with recessive mutations in the same gene.
Data demonstrated that KIF1A promoter methylation can distinguish breast cancer cases from controls in plasma and was inversely associated with DNA repair capacity.
This study establishes an essential role of the CC1 (显示 CCL14 抗体)-FHA (显示 CRY2 抗体) dimer for KIF1A/unc-104-mediated neuronal transport.
The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described.
kinesin family member 1A
, N-3 kinesin
, axonal transporter of synaptic vesicles
, kinesin heavy chain member 1A
, kinesin-like protein KIF1A
, kinesin, heavy chain, member 1A, homolog of mouse
, microtubule-based motor KIF1A
, unc-104- and KIF1A-related protein
, neuron-specific kinesin motor KIF1A