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DAZ2 is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Additionally we are shipping DAZ2 Antibodies (34) and and many more products for this protein.
Studies indicate that partial RNA-binding proteins DAZ1 (show DAZ1 ELISA Kits)/2 deletion was associated wih male infertility, but partial RNA-binding proteins DAZ3 (show DAZ3 ELISA Kits)/4 deletion was not associated with male infertility.
There appears to be an asociation of DAZ1 (show DAZ1 ELISA Kits)/DAZ2 deletion with spermatogenic impairment and male infertility in the South Chinese population.
Deletion of DAZ2 and DAZ4 (show DAZ4 ELISA Kits) gene copies is associated with male infertility.
DAZ gene copy number in severely idiopathic infertile men. Gene deletion of two copies of DAZ (DAZI and 2) was the cause of spermatogenic damage.
All four DAZ genes are expressed in the human testis, and their products are highly polymorphic among men
This gene is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important for spermatogenesis. Four copies of this gene are found on chromosome Y within palindromic duplications\\\\; one pair of genes is part of the P2 palindrome and the second pair is part of the P1 palindrome. Each gene contains a 2.4 kb repeat including a 72-bp exon, called the DAZ repeat\\\\; the number of DAZ repeats is variable and there are several variations in the sequence of the DAZ repeat. Each copy of the gene also contains a 10.8 kb region that may be amplified\\\\; this region includes five exons that encode an RNA recognition motif (RRM) domain. This gene contains one copy of the 10.8 kb repeat. Alternative splicing results in multiple transcript variants encoding different isoforms.
deleted in azoospermia protein 2
, deleted in azoospermia 2
, deleted in azoospermia 4