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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... |