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- 详细信息
- 技术资料
- 靶点:
ACY1
- 浓度:
1 mg/ml
- 应用范围:
WB 1:500~2000, IHC 1:150, FLOW 1:100
- 宿主:
Mouse
- 适应物种:
Human, Mouse, Rat, Dog
- 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:
IgG1
- 免疫原:
Full length human recombinant protein of human ACY1(NP_000657) produced in HEK293 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:ACY-1; ACY1D; HEL-S-5
产品概述:ACY1 (Aminoacylase 1) mouse monoclonal antibody, clone LBI1A12
总结:This gene encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene, as represented in GeneID:100526760. A related pseudogene has been identified on chromosome 18. [provided by RefSeq]
产品概述:ACY1 (Aminoacylase 1) mouse monoclonal antibody, clone LBI1A12
总结:This gene encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene, as represented in GeneID:100526760. A related pseudogene has been identified on chromosome 18. [provided by RefSeq]
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Aminoacylase 1 (ACY1) Mouse Monoclonal Antibody [Clone ID: LBI1A12]
¥690 - 2025


![Aminoacylase 1 (ACY1) Mouse Monoclonal Antibody [Clone ID: LBI1A12]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg)

![C20orf79 (SCP2D1) Mouse Monoclonal Antibody [Clone ID: LBI2B5]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg!wh200)
