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Rabbit Polyclonal LRRTM1 Antibody

  • 中文名: LRRTM1抗体
  • 别    名: Leucine-rich repeat transmembrane neuronal protein 1, LRRTM1
货号: IPDX30534
Price: ¥1180
数量:
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验证与应用

应用及物种
WB 1/1000 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 1/100-1/500 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesLeucine-rich repeat transmembrane neuronal protein 1, LRRTM1
Entrez GeneID347730
WB Predicted band size58.6kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman, Mouse
ImmunogenThis LRRTM1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 88-117 amino acids from the Central region of human LRRTM1.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于LRRTM1抗体的3-4篇参考文献及其简要摘要:

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1. **"An unbiased expression screen reveals synaptogenic activity for LRRTM1"**

*Linhoff MW, Laurén J, Cassidy RM, et al. (Neuron, 2009)*

摘要:本研究通过高通量筛选发现LRRTM1在突触形成中具有关键作用,利用特异性抗体证实其与谷氨酸受体亚基结合,调控突触粘附和分化。

2. **"LRRTM1 interacts with presynaptic neurexins through its ectodomain to promote excitatory synapse development"**

*de Wit J, Sylwestrak E, O’Sullivan ML, et al. (Journal of Cell Biology, 2009)*

摘要:揭示LRRTM1通过胞外域与突触前蛋白neurexin互作,使用抗体阻断实验证明其在兴奋性突触发育中的功能,强调其作为突触组织分子的作用。

3. **"LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia"**

*Francks C, Maegawa S, Laurén J, et al. (Molecular Psychiatry, 2007)*

摘要:通过遗传学分析和LRRTM1抗体标记,发现该基因与偏利手及精神分裂症风险相关,提示其在大脑不对称性和神经精神疾病中的潜在机制。

4. **"LRRTM1 regulates development of excitatory synapses in cultured hippocampal neurons"**

*Siddiqui TJ, Pancaroglu R, Craig AM (Journal of Neuroscience, 2010)*

摘要:利用LRRTM1抗体进行免疫染色和功能研究,证明其在海马神经元突触分化中的必要性,并揭示其缺失导致兴奋性突触传递缺陷。

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以上文献均涉及LRRTM1抗体的应用,涵盖其在突触功能、疾病关联及分子机制中的研究。

背景信息

The LRRTM1 (Leucine-Rich Repeat Transmembrane Neuronal 1) antibody is a tool used to study the LRRTM1 protein, a member of the leucine-rich repeat (LRR) family implicated in synaptic development and plasticity. LRRTM1 is a synaptic adhesion molecule expressed predominantly in neurons, where it localizes to glutamatergic postsynaptic sites. It interacts with presynaptic neurexins and other partners to regulate excitatory synapse formation, AMPA receptor clustering, and synaptic signaling. LRRTM1 is encoded by a maternally silenced, paternally expressed gene on chromosome 2p12. and its genomic imprinting has been linked to altered brain asymmetry and neurodevelopmental disorders. Studies associate LRRTM1 with schizophrenia, autism spectrum disorders, and handedness, though mechanisms remain unclear. The antibody enables detection of LRRTM1 expression patterns in brain tissues and cultured neurons, facilitating research into its role in synaptic connectivity, neurodevelopmental pathways, and disease models. Its applications include immunohistochemistry, Western blotting, and functional studies exploring LRRTM1’s interactions with synaptic partners. Research using LRRTM1 antibodies has advanced understanding of how LRR domain-containing proteins contribute to neural circuit assembly and psychiatric disease susceptibility.

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