acr sc 51504 santa cruz (Santa Cruz Biotechnology)
Structured Review
Acr Sc 51504 Santa Cruz, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 34 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/acrosin/Acrosin+Antibody/pm41866391-112-40-42
Average 93 stars, based on 34 article reviews
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Marker:Article Title: Complete spermatogenesis in intratesticular testis tissue xenotransplants from immature non-human primate Article Snippet: For immunohistochemical staining, dewaxed and rehydrated sections were washed with phosphate-buffered saline (PBS; Life-technologies, Gent, Belgium) and non-specific peroxidase was blocked with 0.3% (v/v) hydrogen peroxide in methanol for 30 min. Antigen retrieval was performed by heating the tissue sections in citrate buffer (0.01 M, pH 6.0) in a water bath (95°C) for 75 min. .. Following another washing step, non-specific adhesion sites were blocked with 4% normal goat serum (Tebu-bio, Boechout, Belgium) diluted in PBS or with Cas-block (Life Technologies) (only for CREM-1 antibody) for 30 min. Next, primary antibodies against VIMENTIN (marmoset specific), MAGE-A4 (mouse monoclonal anti-melanoma-associated antigen 4; dilution 1:200; gift from Dr Spagnoli; marker for spermatogonia and primary spermatocytes, marmoset specific), BOLL (mouse monoclonal anti-BOLL; dilution 1:400; H00066037-M03; R&D system, Abingdon, UK; marker for spermatocytes (meiotic cells)), CREM-1 (rabbit polyclonal anti-CREM-1; dilution 1:400; sc-440; Santa-Cruz Biotechnology, Heidelberg, Germany; marker for round spermatids (post-meiotic cells)) and Incubation:Article Title: Complete spermatogenesis in intratesticular testis tissue xenotransplants from immature non-human primate Article Snippet: For immunohistochemical staining, dewaxed and rehydrated sections were washed with phosphate-buffered saline (PBS; Life-technologies, Gent, Belgium) and non-specific peroxidase was blocked with 0.3% (v/v) hydrogen peroxide in methanol for 30 min. Antigen retrieval was performed by heating the tissue sections in citrate buffer (0.01 M, pH 6.0) in a water bath (95°C) for 75 min. .. Following another washing step, non-specific adhesion sites were blocked with 4% normal goat serum (Tebu-bio, Boechout, Belgium) diluted in PBS or with Cas-block (Life Technologies) (only for CREM-1 antibody) for 30 min. Next, primary antibodies against VIMENTIN (marmoset specific), MAGE-A4 (mouse monoclonal anti-melanoma-associated antigen 4; dilution 1:200; gift from Dr Spagnoli; marker for spermatogonia and primary spermatocytes, marmoset specific), BOLL (mouse monoclonal anti-BOLL; dilution 1:400; H00066037-M03; R&D system, Abingdon, UK; marker for spermatocytes (meiotic cells)), CREM-1 (rabbit polyclonal anti-CREM-1; dilution 1:400; sc-440; Santa-Cruz Biotechnology, Heidelberg, Germany; marker for round spermatids (post-meiotic cells)) and Article Title: Analysis of putative biomarkers of undifferentiated spermatogonia in dog testis. Article Snippet: Spermatogenesis begins after puberty and continues throughout a male’s life, and is regulated by spermatogonial stem cells in the seminiferous tubules.. Markers of male germ cells, including undifferentiated spermatogonia to fully developed spermatozoa have been identified in rodents, but not in dogs.. In this study, to characterize the markers of undifferentiated spermatogonia, histological and immunohistochemical analyses were performed on pre-pubertal (1-month-old), early pubertal (4-month-old), and post-pubertal (7-month-old) dog testes. Bioprocessing:Article Title: Dephosphorylation of protamine 2 at serine 56 is crucial for murine sperm maturation in vivo. Article Snippet: The posttranslational modification of histones is crucial in spermatogenesis, as in other tissues; however, during spermiogenesis, histones are replaced with protamines, which are critical for the tight packaging of the DNA in sperm cells.. Protamines are also posttranslationally modified by phosphorylation and dephosphorylation, which prompted our investigation of the underlying mechanisms and biological consequences of their regulation.. On the basis of a screen that implicated the heat shock protein Hspa4l in spermatogenesis, we generated mice deficient in Hspa4l (Hspa4l-null mice), which showed male infertility and the malformation of sperm heads. |

