ACSM3,丁酰基辅酶A合成酶3抗体-抗体-抗体-生物在线
上海沪震实业有限公司
ACSM3,丁酰基辅酶A合成酶3抗体

ACSM3,丁酰基辅酶A合成酶3抗体

商家询价

产品名称: ACSM3,丁酰基辅酶A合成酶3抗体

英文名称: Anti-ACSM3 antibody

产品编号: HZ-7641R

产品价格: null

产品产地: 中国/美国

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: WB,ELISA,IHC-P,IHC-F,IF

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ACSM3,丁酰基辅酶A合成酶3抗体

产品编号HZ-7641R
英文名称ACSM3
中文名称丁酰基辅酶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0.1ml 0.2ml 
说 明 书0.1ml 0.2ml
研究领域心血管 细胞生物 信号转导
ACSM3,丁酰基辅酶A合成酶3抗体抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat,
产品应用ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量63kDa
细胞定位细胞浆
性 状Lyophilized or Liquid
浓 度1mg/1ml
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.
ACSM3,丁酰基辅酶A合成酶3抗体PubMedPubMed
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)

Subunit:


Subcellular Location:
Mitochondrion matrix

ACSM3,丁酰基辅酶A合成酶3抗体Similarity:
Belongs to the ATP-dependent AMP-binding enzyme family.

Gene ID:
6296

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.