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May have S-adenosyl-L-methionine-dependent methyl- transferase activity (Potential).. Zusätzlich bieten wir Ihnen NOP2/Sun Domain Family, Member 7 Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.
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Sun domain containing protein Nsun7 mutant sperm exhibited depressed progressive motility associated with a rigid flagellar midpiece (but not principal piece) segment
mutant protein structures of Nsun7 indicated that the amino acid serine was converted to alanine, the structure of the helix, coil and strand was changed, and the protein folding and ligand binding sites were changed in samples from asthenospermic men with a transversion mutation in exon 7, indicating impairment of protein function. Because Nsun7 plays a role in sperm motility, mutation in exon 7 may lead to infertility.
Our findings revealed that genetic polymorphisms in exon7 of the NSUN7 gene are not associated with asthenospermia in Chinese Han men.
Nsun7 (A11337)-deletion mutation, causes reduction of its protein rate and associated with sperm motility defect in infertile men.
May have S-adenosyl-L-methionine-dependent methyl- transferase activity (Potential).
NOL1/NOP2/Sun domain family, member 7
, Williams-Beuren syndrome critical region protein 20
, putative methyltransferase NSUN7
, NOL1/NOP2/Sun domain family member 7