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Rabbit抗原名称
Acetyl-CoA Carboxylase分子别名
Acetyl-CoA carboxylase 1; ACC1; Acetyl-Coenzyme A carboxylase alpha (ACC-alpha); ACAC; ACCA; ACACA免疫原
Synthetic Peptide细胞定位
CytoplasmAccession
Q13085克隆号
S-2220-96抗体类型
Recombinant mAb抗体同种型
IgG反应种属 ?
Hu, Ms, Rt阳性样本
HEK-293, A431, HeLa, HepG2, NIH/3T3, mouse brain, C6, rat brain预测反应种属
(反应种属缩写表)Bv, Ck, Sh纯化方式
Protein A浓度
0.5 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
储存条件
12 months from date of receipt / reconstitution, -20 °C as supplied
应用
ICFCM ,IHC-P ? ,ICC ? ,WB稀释度
应用 稀释度 推荐种属 WB 1:1000 Hu, Ms, Rt IHC-P 1:500 Hu, Ms, Rt ICC 1:500 Ms ICFCM 1:50 Ms
Acetyl-CoA Carboxylase (ACC) is a crucial metabolic enzyme that plays a central role in fatty acid metabolism. It catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. ACC exists in two isoforms: ACC1 (ACACA), primarily localized in the cytosol and regulating fatty acid synthesis, and ACC2 (ACACB), which is associated with the outer mitochondrial membrane. The malonyl-CoA produced by ACC2 inhibits carnitine palmitoyltransferase-1 (CPT-1), thereby regulating fatty acid β-oxidation. The enzyme is tightly controlled by multiple mechanisms, including allosteric regulation (activation by citrate, inhibition by long-chain acyl-CoA), reversible phosphorylation (inactivation by AMPK and PKA), and transcriptional regulation (e.g., SREBP-1c-mediated expression upregulation). Due to its pivotal role in energy metabolism, ACC is a potential therapeutic target for obesity, diabetes, and cancer, with inhibitors (e.g., TOFA, ND-630) currently under investigation. Additionally, plant and bacterial ACCs are targets for herbicides (e.g., aryloxyphenoxypropionates) and antibiotics, highlighting their broad biological significance.
免疫印迹
WB result of Acetyl-CoA Carboxylase Recombinant Rabbit mAb
Primary antibody: Acetyl-CoA Carboxylase Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: HEK-293 whole cell lysate 20 µg
Lane 2: A431 whole cell lysate 20 µg
Lane 3: HeLa whole cell lysate 20 µg
Lane 4: HepG2 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 266 kDa
Observed MW: 266 kDaWB result of Acetyl-CoA Carboxylase Recombinant Rabbit mAb
Primary antibody: Acetyl-CoA Carboxylase Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: NIH/3T3 whole cell lysate 20 µg
Lane 2: mouse brain lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 266 kDa
Observed MW: 266 kDaWB result of Acetyl-CoA Carboxylase Recombinant Rabbit mAb
Primary antibody: Acetyl-CoA Carboxylase Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: C6 whole cell lysate 20 µg
Lane 2: rat brain lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 266 kDa
Observed MW: 266 kDa
流式分析
Flow cytometric analysis of 4% PFA fixed 90% methanol permeabilized NIH/3T3 (Mouse embryonic fibroblast) labelling Acetyl-CoA antibody at 1/50 dilution (1 μg) / (Red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti - Rabbit IgG Alexa Fluor® 488 was used as the secondary antibody.
免疫组化
IHC shows positive staining in paraffin-embedded human stomach. Anti- Acetyl-CoA Carboxylase antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human hepatocellular carcinoma. Anti- Acetyl-CoA Carboxylase antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded mouse kidney. Anti- Acetyl-CoA Carboxylase antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded rat stomach. Anti- Acetyl-CoA Carboxylase antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
免疫细胞化学
ICC shows positive staining in NIH/3T3 cells. Anti- Acetyl-CoA Carboxylase antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
组织表达图谱
Expression of Acetyl-CoA Carboxylase in tumor tissue.
Expression of Acetyl-CoA Carboxylase in human tissue.
Expression of Acetyl-CoA Carboxylase in mouse & rat tissue.
FAQs
我们一般不推荐客户回收利用抗体。 因为抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。另外,我们对一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定

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