phospho-Acetyl Coenzyme A Carboxylase alpha (Ser1263) antibody产品图

phospho-Acetyl Coenzyme A Carb

oxylase alpha (Ser1263) antibody
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  • ¥1580
  • 康朗生物
  • kl-12955R
  • 中国/美国/德国
  • 2025年07月10日
  • WB=1:500-2000 ELISA=1:500-1000
  • Rabbit
  • Human
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 供应商:

      上海康朗生物科技有限公司

    • 库存:

      大量

    • 目录编号:

      kl-12955R

    • 克隆性:

      多克隆

    • 抗原来源:

      Rabbit

    • 保质期:

      12个月

    • 抗体英文名:

      phospho-Acetyl Coenzyme A Carboxylase alpha (Ser1263) antibody

    • 抗体名:

      磷酸化乙酰辅酶A羧化酶抗体

    • 宿主:

      Rabbit

    • 适应物种:

      Human

    • 免疫原:

      KLH conjugated synthesised phosphopeptide derived from human Acetyl Coenzyme A Carboxylase alpha around the phosphorylation site of Ser1263:PQ(p-S)PT

    • 亚型:

      IgG

    • 形态:

      冻干粉或液体

    • 应用范围:

      WB=1:500-2000 ELISA=1:500-1000

    • 浓度:

      1mg/ml

    • 保存条件:

      -20 °C

    • 规格:

      100ul

    phospho-Acetyl Coenzyme A Carboxylase alpha (Ser1263) antibody
    中文名称 磷酸化乙酰辅酶A羧化酶抗体
    别    名 Acetyl Coenzyme A Carboxylase alpha (phospho S1263); p-Acetyl Coenzyme A Carboxylase alpha (phospho S1263); ACAC; ACACA; ACACA; ACACA_HUMAN; ACC alpha; ACC; ACC-alpha; ACC1; ACC1; ACCA; acetyl CoA carboxylase 1; acetyl Coenzyme A; Acetyl Coenzyme A; Biotin carboxylase; Acetyl-Coenzyme A Carboxylase alpha.  
    规格价格 100ul/1580元 购买        大包装/询价
    说 明 书 100ul  
    产品类型 磷酸化抗体 
    研究领域 肿瘤  心血管  细胞生物  转录调节因子  
    抗体来源 Rabbit
    克隆类型 Polyclonal
    交叉反应 Human, 
    产品应用 WB=1:500-2000 ELISA=1:500-1000 (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 265kDa
    细胞定位 细胞浆 
    性    状 Lyophilized or Liquid
    浓    度 1mg/ml
    免 疫 原 KLH conjugated synthesised phosphopeptide derived from human Acetyl Coenzyme A Carboxylase alpha around the phosphorylation site of Ser1263:PQ(p-S)PT 
    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.
    PubMed PubMed
    产品介绍 background:
    Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. There are two ACC forms, alpha and beta, encoded by two different genes. ACC-alpha is highly enriched in lipogenic tissues. The enzyme is under long term control at the transcriptional and translational levels and under short term regulation by the phosphorylation/dephosphorylation of targeted serine residues and by allosteric transformation by citrate or palmitoyl-CoA. Multiple alternatively spliced transcript variants divergent in the 5' sequence and encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

    Function:
    Catalyzes the rate-limiting reaction in the biogenesis of long-chain fatty acids. Carries out three functions: biotin carboxyl carrier protein, biotin carboxylase and carboxyltransferase.

    Subunit:
    Monomer, homodimer, and homotetramer. Can form filamentous polymers. Interacts in its inactive phosphorylated form with the BRCT domains of BRCA1 which prevents ACACA dephosphorylation and inhibits lipid synthesis. Interacts with MID1IP1; interaction with MID1IP1 promotes oligomerization and increases its activity.

    Subcellular Location:
    Cytoplasm.

    Tissue Specificity:
    Expressed in brain, placental, skeletal muscle, renal, pancreatic and adipose tissues; expressed at low level in pulmonary tissue; not detected in the liver.

    Post-translational modifications:
    Phosphorylation on Ser-1263 is required for interaction with BRCA1.

    DISEASE:
    Defects in ACACA are a cause of acetyl-CoA carboxylase 1 deficiency (ACACAD) [MIM:613933]; also known as ACAC deficiency or ACC deficiency. An inborn error of de novo fatty acid synthesis associated with severe brain damage, persistent myopathy and poor growth.

    Similarity:
    Contains 1 ATP-grasp domain.
    Contains 1 biotin carboxylation domain.
    Contains 1 biotinyl-binding domain.
    Contains 1 carboxyltransferase domain.

    SWISS:
    O00763

    Gene ID:
    31

    Database links:

    Entrez Gene: 31 Human

    Entrez Gene: 32 Human

    Entrez Gene: 107476 Mouse

    Entrez Gene: 60581 Rat

    Omim: 200350 Human

    SwissProt: O00763 Human

    SwissProt: Q13085 Human

    SwissProt: Q5SWU9 Mouse

    SwissProt: P11497 Rat

    Unigene: 160556 Human

    Unigene: 234898 Human

    Unigene: 31374 Mouse

    Unigene: 163753 Rat

    Unigene: 217177 Rat

    Unigene: 44372 Rat



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

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