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Rabbit Anti-GFOD2 antibody
Rabbit Anti-GFOD2 antibody
GFOD2; GFOD2_HUMAN; Glucose fructose oxidoreductase domain containing 2; Glucose fructose oxidoreductase domain containing protein 2; Glucose-fructose oxidoreductase domain-containing protein 2; MGC11335.
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  • NO.:SL8405R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,)
    Applications:WB ELISA IHC-P IHC-F IF
    concentration:1mg/ml
  • Goods click count:21
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Details

Product Name GFOD2
Chinese Name 葡萄糖果糖还原酶2抗体
Alias GFOD2; GFOD2_HUMAN; Glucose fructose oxidoreductase domain containing 2; Glucose fructose oxidoreductase domain containing protein 2; Glucose-fructose oxidoreductase domain-containing protein 2; MGC11335.  
Research Area Tumour  Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Rabbit, Sheep, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 40kDa
Cellular localization Extracellular matrix Secretory protein 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human GFOD2: 301-385/385 
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 GFOD2 is a 385 amino acid secreted protein of the extracellular matrix that belongs to the gfo/idh/mocA family. Existing as two alternatively spliced isoforms, GFOD2 enhances matrix assembly and is encoded by a gene that maps to human chromosome 16q22.1. Chromosome 16 encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Function:
Promotes matrix assembly (By similarity).

Subcellular Location:
Secreted, extracellular space, extracellular matrix (By similarity).

Similarity:
Belongs to the Gfo/Idh/MocA family.

SWISS:
Q3B7J2

Gene ID:
81577

Database links:

Entrez Gene: 81577 Human

SwissProt: Q3B7J2 Human

Unigene: 307084 Human



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