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Rabbit Anti-LRGUK antibody
Rabbit Anti-LRGUK antibody
FLJ32786; Leucine-rich repeat and guanylate kinase domain-containing protein; LRGUK; LRGUK_HUMAN.
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  • NO.:SL18357R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Mouse,(predicted: Human,Rat,Pig,)
    Applications:ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name LRGUK
Chinese Name LRGUK蛋白抗体
Alias FLJ32786; Leucine-rich repeat and guanylate kinase domain-containing protein; LRGUK; LRGUK_HUMAN.  
Research Area Cell biology  Neurobiology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Mouse,  (predicted: Human, Rat, Pig, )
Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=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 93kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human LRGUK: 461-560/825 
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 LRGUK is an 825 amino acid protein that contains a guanylate kinase-like domain, a LRRCT domain and nine LRR (leucine-rich) repeats. The gene encoding LRGUK is located on human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

Similarity:
Contains 1 guanylate kinase-like domain.
Contains 9 LRR (leucine-rich) repeats.
Contains 1 LRRCT domain.

SWISS:
Q96M69

Gene ID:
136332

Database links:

Entrez Gene: 136332 Human

SwissProt: Q96M69 Human

Unigene: 149774 Human



Product Picture
Paraformaldehyde-fixed, paraffin embedded (mouse testis); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (LRGUK) Polyclonal Antibody, Unconjugated (SL18357R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.

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