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KIF7 is a 1,343 amino acid protein expressed in embryonic stem cells, melanotic melanoma and Jurkat T-cells. KIF7 is a member of the KIF27 subfamily of the kinesin-like protein family and contains one kinesin-motor domain. It is suggested that KIF7 may participate in the Hedgehog (Hh) signaling pathway by regulating the proteolysis and stability of GLI transcription factors. Hedgehog (Hh) signaling plays a critical role in embryonic development.
更新時(shí)間：2025-03-06
型號(hào)：bs-12388R-Bio
廠商性質(zhì)：生產(chǎn)廠家
瀏覽量：77
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted “Glycine X Y“ triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth
更新時(shí)間：2025-03-06型號(hào)：bs-10423R-PE廠商性質(zhì)：生產(chǎn)廠家瀏覽量：108
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted “Glycine X Y“ triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth
更新時(shí)間：2025-03-06型號(hào)：bs-10423R-APC廠商性質(zhì)：生產(chǎn)廠家瀏覽量：89
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted “Glycine X Y“ triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth
更新時(shí)間：2025-03-06型號(hào)：bs-10423R-Cy5廠商性質(zhì)：生產(chǎn)廠家瀏覽量：89
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted “Glycine X Y“ triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth
更新時(shí)間：2025-03-06型號(hào)：bs-10423R-Cy3廠商性質(zhì)：生產(chǎn)廠家瀏覽量：98
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted “Glycine X Y“ triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth
更新時(shí)間：2025-03-06型號(hào)：bs-10423R-FITC廠商性質(zhì)：生產(chǎn)廠家瀏覽量：110
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