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Rabbit Anti-Ketohexokinase antibody
Rabbit Anti-Ketohexokinase antibody
fructokinase; Hepatic fructokinase; ketohexokinase; Ketohexokinase isoform a; KHK; EC 2.7.1.3; KHK_HUMAN.
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  • NO.:SL4045R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Pig,Cow,Horse,Rabbit,)
    Applications:WB ELISA IHC-P IHC-F IF
    concentration:1mg/ml
  • Goods click count:25
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Details

Product Name Ketohexokinase
Chinese Name 肝果糖激酶抗体
Alias fructokinase; Hepatic fructokinase; ketohexokinase; Ketohexokinase isoform a; KHK; EC 2.7.1.3; KHK_HUMAN.   
Research Area Tumour  Cell biology  immunology  transcriptional regulatory factor  Kinases and Phosphatases  glycoprotein  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Pig, Cow, Horse, Rabbit, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 33kDa
Cellular localization cytoplasmic Extracellular matrix 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human Ketohexokinase: 151-250/298 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail 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:
P50053

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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