MFRP (GeneName), Membrane frizzled-related protein (ProteinName), MFRP_HUMAN.
Human MFRP/ Membrane frizzled-related protein ELISA Kit
Membrane-type frizzled-related protein
Natural and recombinant human Membrane frizzled-related protein
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Interacts with C1QTNF5.
May play a role in eye development.
Apical cell membrane Single-pass type II membrane protein
MKDFSDVILC | MEATESSKTE | FCNPAFEPES | GPPCPPPVFP | EDASYSVPAP |
WHGRRPRGLR | PDCRFSWLCV | LLLSSLLLLL | LGLLVAIILA | QLQAAPPSGA |
SHSPLPAGGL | TTTTTTPTIT | TSQAAGTPKG | QQESGVSPSP | QSTCGGLLSG |
PRGFFSSPNY | PDPYPPNTHC | VWHIQVATDH | AIQLKIEALS | IESVASCLFD |
RLELSPEPEG | PLLRVCGRVP | PPTLNTNASH | LLVVFVSDSS | VEGFGFHAWY |
QAMAPGRGSC | AHDEFRCDQL | ICLLPDSVCD | GFANCADGSD | ETNCSAKFSG |
CGGNLTGLQG | TFSTPSYLQQ | YPHQLLCTWH | ISVPAGHSIE | LQFHNFSLEA |
QDECKFDYVE | VYETSSSGAF | SLLGRFCGAE | PPPHLVSSHH | ELAVLFRTDH |
GISSGGFSAT | YLAFNATENP | CGPSELSCQA | GGCKGVQWMC | DMWRDCTDGS |
DDNCSGPLFP | PPELACEPVQ | VEMCLGLSYN | TTAFPNIWVG | MITQEEVVEV |
LSGYKSLTSL | PCYQHFRRLL | CGLLVPRCTP | LGSVLPPCRS | VCQEAEHQCQ |
SGLALLGTPW | PFNCNRLPEA | ADLEACAQP
This product has not yet been referenced specifically in any publications.
"Molecular cloning and characterization of MFRP, a novel gene encoding a membrane-type Frizzled-related protein."
"Evaluation of MFRP as a candidate gene for high hyperopia."
"Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia."
"Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyes."
"A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation."
"Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations."
"Identification of MFRP Mutations in Chinese Families with High Hyperopia."
"A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy."
"Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex."
"Developmental basis of nanophthalmos: MFRP Is required for both prenatal ocular growth and postnatal emmetropization."
Displaying results : 0
No feedback yet, let's comment.
Product Name *
Size Quantity Price ($) Subtotal 1 ($)
Subtotal 2: $
Size Quantity Price ($)
Do you want to be our agent and get a lower discount?
Please contact us:
Please contact us: