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產(chǎn)品分類 / PRODUCT

Anti-ADK抗體
描述:

Anti-ADK抗體銅轉運蛋白質β鏈是銅轉運蛋白質家族中的一種,可調節(jié)細胞內銅離子水平的銅轉運P型三磷酸腺苷酶,ATP7B是生物體內廣泛存在的一種極為重要的細胞膜上的酶,它的功能主要是維持細胞內外的離子及滲透壓平衡、跨膜電化學和細胞的能量代謝.

  • 產(chǎn)品型號:
  • 廠商性質:生產(chǎn)廠家
  • 更新時間:2025-12-10
  • 訪問量:164
產(chǎn)品介紹/ PRODUCT PRESENTATION

產(chǎn)品編號 byb-2778R
英文名稱 Anti-ADK抗體
中文名稱 腺苷酸激酶抗體
別    名 Adenosine kinase; AK; 5033405D03Rik; AI255373; AI987814; MGC6593; 2310026J05Rik; Adenosine 5'-phosphotransferase; OTTHUMP00000019864; OTTHUMP00000019865; ADK_HUMAN; Adenosine kinase; AK; Full=Adenosine 5'-phosphotransferase.
Anti-ADK抗體  
說 明 書 0.1ml  0.2ml  
研究領域 激酶和磷酸酶  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse, Rat, Chicken, Dog, Pig, Cow, 
產(chǎn)品應用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復) 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 41kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human ADK/adenylate kinase
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 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
產(chǎn)品介紹 background:
widespread effects on the cardiovascular, nervous, respiratory, and immune systems and inhibitors of ADK could play an important pharmacological role in increasing intravascular adenosine concentrations and acting as antiinflammatory agents. The encoded protein does not present any sequence similarities to other well characterized mammalian nucleoside kinases. In contrast, 2 regions were identified with significant sequence identity to microbial ribokinase and fructokinases and a bacterial inosine/guanosine kinase. Thus, ADK is a structurally distinct mammalian nucleoside kinase that appears to be akin to sugar kinases of microbial origin. Animal studies have demonstrated that a deficiency of adenosine metabolism a powerful contributor to the development of neonatal hepatic steatosis, providing a model for the rapid development of postnatally lethal fatty liver.

Function:
ATP dependent phosphorylation of adenosine and other related nucleoside analogs to monophosphate derivatives. Serves as a potential regulator of concentrations of extracellular adenosine and intracellular adenine nucleotides.

Subunit:
Monomer.

Tissue Specificity:
Widely expressed. Highest level in placenta, liver, muscle and kidney.

DISEASE:
Hypermethioninemia due to adenosine kinase deficiency (HMAKD) [MIM:614300]: A metabolic disorder characterized by global developmental delay, early-onset seizures, mild dysmorphic features, and characteristic biochemical anomalies, including persistent hypermethioninemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine. Homocysteine levels are typically normal. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the carbohydrate kinase PfkB family.


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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