FITC标记的丁酰基辅酶A合成酶3抗体
产品名称： FITC标记的丁酰基辅酶A合成酶3抗体
英文名称： Anti-ACSM3/FITC
产品编号： HZ-7641R-FITC
产品价格： null
产品产地： 中国/上海
品牌商标： HZbscience
更新时间： 2023-08-17T10:24:20
使用范围： IF=1:50-200
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Rabbit Anti-ACSM3/FITC Conjugated antibody
FITC标记的丁酰基辅酶A合成酶3抗体
| 英文名称 | Anti-ACSM3/FITC |
| 中文名称 | FITC标记的丁酰基辅酶A合成酶3抗体 |
| 别 名 | Butyryl coenzyme A synthetase 3; mitochondrial; ACSM3; ACSM3_HUMAN; Acyl CoA synthetase medium chain family member 3; Acyl-CoA synthetase medium-chain family member 3; Acyl-coenzyme A synthetase ACSM3; Acyl-coenzyme A synthetase ACSM3, mitochondrial; Butyrate CoA ligase 3; Butyrate--CoA ligase 3; Butyryl-coenzyme A synthetase 3; Middle chain acyl CoA synthetase 3; Middle-chain acyl-CoA synthetase 3; Protein SA homolog; SA (rat hypertension associated) homolog; SA antibody SA hypertension associated homolog; SA, rat, homolog of; SAH. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 心血管 细胞生物 信号转导 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, Rat, |
| 产品应用 | IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 63kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human ACSM3 |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| 产品介绍 | background: ACSM3 is a 586 amino acid protein has a broad substrate specificity and utilizes magnesium as a cofactor. The gene encoding ACSM3 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition. Function: Has medium-chain fatty acid:CoA ligase activity with broad substrate specificity (in vitro). Acts on acids from C(4) to C(11) and on the corresponding 3-hydroxy- and 2,3- or 3,4-unsaturated acids (in vitro) Subcellular Location: Mitochondrion matrix Similarity: Belongs to the ATP-dependent AMP-binding enzyme family. Database links: Entrez Gene: 6296 Human Entrez Gene: 20216 Mouse Omim: 145505 Human SwissProt: Q53FZ2 Human SwissProt: Q3UNX5 Mouse Unigene: 706754 Human Unigene: 334199 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
ACSM3是一种具有广泛底物特异性和利用镁作为辅因子的586氨基酸蛋白。编码AcSM3的基因映射到人类16号染色体上，编码900个以上的基因并包含人类基因组的近3%。GaN基因位于16号染色体上，具有突变，可能导致巨大轴突神经病变，神经系统疾病的特征是随着生长的增加而增加。罕见的Rubinstein Taybi综合征也与16号染色体相关，如Crohn氏病，这是胃肠道炎症状态。