![L1CAM Mouse Monoclonal Antibody [Clone ID: LBI1G4]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg)
- ￥690 - 2025
- Leading Biology
- AMM10032V
- 美国
- 2025年07月11日
- WB 1:2000, IF 1:100, FLOW 1:100
- Mouse
- Human, Mouse, Rat
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- 详细信息
- 技术资料
- 靶点：
L1CAM
- 浓度：
1 mg/ml
- 应用范围：
WB 1:2000, IF 1:100, FLOW 1:100
- 宿主：
Mouse
- 适应物种：
Human, Mouse, Rat
- 保质期：
1-2年
- 供应商：
安诺伦（北京）生物科技有限公司
- 标记物：
Unconjugated
- 克隆性：
Monoclonal Antibody
- 保存条件：
Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
- 形态：
PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
- 亚型：
IgG2a
- 免疫原：
Full length human recombinant protein of human L1CAM (NP_000416) produced in HEK293T cell.
- 规格：
100 ul/30 ul
| 规格： | 100 ul | 产品价格： | ￥2025.0 |
|---|---|---|---|
| 规格： | 30 ul | 产品价格： | ￥690.0 |
别名：CAML1; CD171; HSAS; HSAS1; MASA; MIC5; N-CAM-L1; N-CAML1; NCAM-L1; S10; SPG1
产品概述：L1CAM mouse monoclonal antibody, clone LBI1G4
总结：The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause three X-linked neurological syndromes known by the acronym CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of a neuron-specific exon is thought to be functionally relevant. [provided by RefSeq]
产品概述：L1CAM mouse monoclonal antibody, clone LBI1G4
总结：The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause three X-linked neurological syndromes known by the acronym CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of a neuron-specific exon is thought to be functionally relevant. [provided by RefSeq]
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L1CAM Mouse Monoclonal Antibody [Clone ID: LBI1G4]
￥690 - 2025
