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BOLL belongs to the DAZ gene family required for germ cell development. Additionally we are shipping BOLL Proteins (5) and many more products for this protein.
Showing 10 out of 76 products:
Human Polyclonal BOLL Primary Antibody for EIA, WB - ABIN950673
Chen, Ma, Li, Zhang, Su, Ma, Liu, Tao, Lin, Yang: Phenotypic expression of partial AZFc deletions is independent of the variations in DAZL and BOULE in a Han population. in Journal of andrology 2010
Show all 4 references for 950673
Human Polyclonal BOLL Primary Antibody for ELISA, IHC - ABIN268678
Lin, Chung, Cheng: Posttranscriptional regulation of CDC25A by BOLL is a conserved fertility mechanism essential for human spermatogenesis. in The Journal of clinical endocrinology and metabolism 2009
Show all 2 references for 268678
Human Polyclonal BOLL Primary Antibody for IHC, ELISA - ABIN185072
Xu, Moore, Pera: A gene family required for human germ cell development evolved from an ancient meiotic gene conserved in metazoans. in Proceedings of the National Academy of Sciences of the United States of America 2001
Cow (Bovine) Polyclonal BOLL Primary Antibody for WB - ABIN2776601
Kostova, Yeung, Luetjens, Brune, Nieschlag, Gromoll: Association of three isoforms of the meiotic BOULE gene with spermatogenic failure in infertile men. in Molecular human reproduction 2007
Our study demonstrated an oncogenic role of BOLL in CRC (show CALR Antibodies) despite tumor-specific promoter hypermethylation.
demonstrate that Boll is also transiently expressed during oogenesis in the fetal mouse ovary, but is simultaneously co-expressed within the same germ cells as Dazl (show DAZL Antibodies)
Assessing the expression of both CDY1 (show CDY2A Antibodies) and BOULE by qualitative RT-PCR is a sensitive and feasible test for predicting the presence of sperm cells in testicular tissue biopsies.
expression of spermatogenic phenotypes of partial AZFc deletions is independent of the variations in DAZL and BOULE in the Han population
BOULE may encode a key conserved switch that regulates progression of germ cells through meiosis in men.
Role in spermatogenesis. Decreased DAZ proteins in spermatogenic failure may be due to germ cell loss. Transcription of BOULE, DAZL, and DAZ not altered in degrees of spermatogenic failure. No increase of DAZL or BOULE found in DAZ deletion.
Major group of infertile men with meiotic arrest lack BOULE protein and its putative target, CDC25A (show CDC25A Antibodies) expression. Spermatogenic failure may arise from factor(s) upstream of BOULE possibly involved in regulating transcription and/or translation of BOULE.
BOULE coding sequence mutations are not an important factor in the aetiology of azoospermia.
mutations in BOULE can be eliminated as a major cause of impaired spermatogenesis.
Among the three BOULE isoforms, B2 might have the major role for meiotic completion.
The b-boule gene is predicted to encode a polypeptide of 295 amino acids with an RNP (show RNPC3 Antibodies)-type RNA recognition domain. Tertiary structure analysis shows that b-boule binds specifically to polypyrimidine RNAs.
asked whether BOULE, the founding member of DAZ family proteins, is a component of the SGs (show SKI Antibodies). We show that BOULE is recruited to the SGs (show SKI Antibodies) upon heat stress, and that these SGs (show SKI Antibodies) are developmental stage-specific
These results showed that IGF1 (show IGF1 Antibodies) regulated the expression of BOULE and CDC25A (show CDC25A Antibodies) mRNAs via ERK1/2 (show MAPK1/3 Antibodies) signaling and in T-independent pathway during spermatogenesis in the adult mouse testes.
Expression of key regulators of spermiogenesis was unaffected in Boule(-/-) mice, suggesting that Boule regulates germ-cell differentiation through a novel pathway.
This gene belongs to the DAZ gene family required for germ cell development. It encodes an RNA-binding protein which is more similar to Drosophila Boule than to human proteins encoded by genes DAZ (deleted in azoospermia) or DAZL (deleted in azoospermia-like). Loss of this gene function results in the absence of sperm in semen (azoospermia). Histological studies demonstrated that the primary defect is at the meiotic G2/M transition. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.