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Search Results for " evr1 "

7

Recombinant Proteins

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPY-04302 Frizzled 4 Protein, Human, Recombinant (His) Human HEK293 Cells
Familial exudative vitreoretinopathy (FEVR) is a hereditary blinding disorder that features defects in retinal vascular development. Mutations in FZD4 are known to cause autosomal dominant exudative vitreoretinopathy (EV...
TMPY-00197 Frizzled 4 Protein, Human, Recombinant (hFc) Human HEK293 Cells
Familial exudative vitreoretinopathy (FEVR) is a hereditary blinding disorder that features defects in retinal vascular development. Mutations in FZD4 are known to cause autosomal dominant exudative vitreoretinopathy (EV...
TMPK-00740 LRP-5 Protein, Human, Recombinant (mFc) Human HEK293 Cells
A role for low-density lipoprotein-related receptor 5 (LRP5) in human bone was first established by the identification of genetic alterations that led to dramatic changes in bone mass. Shortly thereafter, mutations that ...
TMPK-00739 LRP-5 Protein, Human, Recombinant (hFc) Human HEK293 Cells
A role for low-density lipoprotein-related receptor 5 (LRP5) in human bone was first established by the identification of genetic alterations that led to dramatic changes in bone mass. Shortly thereafter, mutations that ...
TMPY-06639 LRP-5 Protein, Human, Recombinant (His) Human HEK293 Cells
LRP-5 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 71.21 kDa and the accession number is O75197-1.
TMPY-00313 Frizzled 4 Protein, Rat, Recombinant (His) Rat HEK293 Cells
Familial exudative vitreoretinopathy (FEVR) is a hereditary blinding disorder that features defects in retinal vascular development. Mutations in FZD4 are known to cause autosomal dominant exudative vitreoretinopathy (EV...
TMPY-03310 Frizzled 4 Protein, Rat, Recombinant (hFc) Rat HEK293 Cells
Familial exudative vitreoretinopathy (FEVR) is a hereditary blinding disorder that features defects in retinal vascular development. Mutations in FZD4 are known to cause autosomal dominant exudative vitreoretinopathy (EV...
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