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Ketohexokinase Rabbit pAb (bs-4045R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-4045R
英文名稱 Ketohexokinase Rabbit pAb
中文名稱 肝果糖激酶抗體
別    名 fructokinase; Hepatic fructokinase; ketohexokinase; Ketohexokinase isoform a; KHK; EC 2.7.1.3; KHK_HUMAN.  
研究領域 腫瘤  細胞生物  免疫學  轉錄調節因子  激酶和磷酸酶  糖蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Horse)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 33 kDa
檢測分子量
細胞定位 細胞漿 細胞外基質 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Ketohexokinase: 151-250/298 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 This gene encodes ketohexokinase that catalyzes conversion of fructose to fructose-1-phosphate. The product of this gene is the first enzyme with a specialized pathway that catabolizes dietary fructose. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Subunit:
Homodimer.

Tissue Specificity:
Most abundant in liver, kidney, gut, spleen and pancreas. Low levels also found in adrenal, muscle, brain and eye.

DISEASE:
Defects in KHK are the cause of fructosuria (FRUCT) [MIM:229800]. Benign defect of intermediary metabolism.

Similarity:
Belongs to the carbohydrate kinase PfkB family.

SWISS:
Q6IBK2

Gene ID:
3795

Database links:

Entrez Gene: 3795 Human

Entrez Gene: 16548 Mouse

Omim: 614058 Human

SwissProt: P50053 Human

SwissProt: Q6IBK2 Human

SwissProt: P97328 Mouse

Unigene: 567297 Human

Unigene: 22451 Mouse



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