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May have S-adenosyl-L-methionine-dependent methyl- transferase activity (Potential).. Additionally we are shipping and many more products for this protein.
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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
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