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acr sc 51504 santa cruz  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology acr sc 51504 santa cruz
    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
    acr sc 51504 santa cruz - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    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 ACROSIN (rabbit polyclonal anti-ACROSIN; dilution 1:500; sc-67151; Santa-Cruz; marker for acrosome visualisation in round, elongating and elongated spermatids (post-meiotic cells), marmoset specific), were applied to the sections and incubated in a humidified chamber overnight at 4°C. .. After washing, sections were incubated with a peroxidase-labelled secondary antibody (Dako Real Envision Detection System; Dako) for 1 h. Staining was visualised with 3,3′-diaminobenzidine (Dako RealTM EnvisionTM Envision system; Dako) as the chromogen and haematoxylin as the counterstain.

    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 ACROSIN (rabbit polyclonal anti-ACROSIN; dilution 1:500; sc-67151; Santa-Cruz; marker for acrosome visualisation in round, elongating and elongated spermatids (post-meiotic cells), marmoset specific), were applied to the sections and incubated in a humidified chamber overnight at 4°C. .. After washing, sections were incubated with a peroxidase-labelled secondary antibody (Dako Real Envision Detection System; Dako) for 1 h. Staining was visualised with 3,3′-diaminobenzidine (Dako RealTM EnvisionTM Envision system; Dako) as the chromogen and haematoxylin as the counterstain.

    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.



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    Histology of testes from normal and busulfan-treated mice and identification of developed cells in the MCS. Testes from immature mice (7-day-old) (normal mice; A ) or from busulfan-injected mice (10 days post injection of the immature mice) (BU-treated mice; B ) were fixed in Bouin’s solution and stained with hematoxylin–eosin for histological examination. Cells were enzymatically isolated from the testes of mice described above and were cultured for 5 weeks in methylcellulose 3D culture (MCS) containing StemPro Medium, various growth factors, and KSR 10% (see in the absence (CT) or presence of IL-1β (1, 10, and 100 pg/mL) (IL-1β). The morphologies of cultures (from normal and BU-treated mice) in the absence (CT) or presence of IL-1β (IL-1β) after 5 weeks show the presence of cells and organoids ( B ). Developed cells from normal ( C ) and busulfan-treated mice ( D ) were collected after 5 weeks, fixed, and stained with specific antibodies to markers specific for the different stages of spermatogenesis, such as the pre-meiotic marker (Vasa and GFRα), meiotic marker (Boule), and post-meiotic marker <t>(acrosin).</t> DAPI (blue) was used for nucleus staining (NC, negative control; BC, before culture; CT, control (without IL-1β)). Cultures were grown in the presence of different concentrations of IL-1β (1, 10, 100 pg/mL) (IL-1β). The number of repeated experiments was (N) = 4–5, and the number of wells for each treatment in each experiment was ( n ) = 3. We present pictures representative of the experiments.
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    Mean value and standard deviation (StD) of the ( a ) optical density and ( b ) <t>acrosin</t> content of soot-free (control) and soot-treated semen after Human Acrosin <t>ELISA</t> Kit assays. Both figures reveal similar tendencies, but the difference between control and soot-treated samples in b is more pronounced due to a cumulative effect, since the OD-acrosin dependence is logarithmic (see ). The large StD in control specimens reflects the inherent diversity of native human ejaculates of all patients involved in the study (see ).
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    Image Search Results


    Histology of testes from normal and busulfan-treated mice and identification of developed cells in the MCS. Testes from immature mice (7-day-old) (normal mice; A ) or from busulfan-injected mice (10 days post injection of the immature mice) (BU-treated mice; B ) were fixed in Bouin’s solution and stained with hematoxylin–eosin for histological examination. Cells were enzymatically isolated from the testes of mice described above and were cultured for 5 weeks in methylcellulose 3D culture (MCS) containing StemPro Medium, various growth factors, and KSR 10% (see in the absence (CT) or presence of IL-1β (1, 10, and 100 pg/mL) (IL-1β). The morphologies of cultures (from normal and BU-treated mice) in the absence (CT) or presence of IL-1β (IL-1β) after 5 weeks show the presence of cells and organoids ( B ). Developed cells from normal ( C ) and busulfan-treated mice ( D ) were collected after 5 weeks, fixed, and stained with specific antibodies to markers specific for the different stages of spermatogenesis, such as the pre-meiotic marker (Vasa and GFRα), meiotic marker (Boule), and post-meiotic marker (acrosin). DAPI (blue) was used for nucleus staining (NC, negative control; BC, before culture; CT, control (without IL-1β)). Cultures were grown in the presence of different concentrations of IL-1β (1, 10, 100 pg/mL) (IL-1β). The number of repeated experiments was (N) = 4–5, and the number of wells for each treatment in each experiment was ( n ) = 3. We present pictures representative of the experiments.

    Journal: International Journal of Molecular Sciences

    Article Title: Effect of IL-1β on the Development of Spermatogenesis In Vitro in Normal and Busulfan-Treated Immature Mice

    doi: 10.3390/ijms25094926

    Figure Lengend Snippet: Histology of testes from normal and busulfan-treated mice and identification of developed cells in the MCS. Testes from immature mice (7-day-old) (normal mice; A ) or from busulfan-injected mice (10 days post injection of the immature mice) (BU-treated mice; B ) were fixed in Bouin’s solution and stained with hematoxylin–eosin for histological examination. Cells were enzymatically isolated from the testes of mice described above and were cultured for 5 weeks in methylcellulose 3D culture (MCS) containing StemPro Medium, various growth factors, and KSR 10% (see in the absence (CT) or presence of IL-1β (1, 10, and 100 pg/mL) (IL-1β). The morphologies of cultures (from normal and BU-treated mice) in the absence (CT) or presence of IL-1β (IL-1β) after 5 weeks show the presence of cells and organoids ( B ). Developed cells from normal ( C ) and busulfan-treated mice ( D ) were collected after 5 weeks, fixed, and stained with specific antibodies to markers specific for the different stages of spermatogenesis, such as the pre-meiotic marker (Vasa and GFRα), meiotic marker (Boule), and post-meiotic marker (acrosin). DAPI (blue) was used for nucleus staining (NC, negative control; BC, before culture; CT, control (without IL-1β)). Cultures were grown in the presence of different concentrations of IL-1β (1, 10, 100 pg/mL) (IL-1β). The number of repeated experiments was (N) = 4–5, and the number of wells for each treatment in each experiment was ( n ) = 3. We present pictures representative of the experiments.

    Article Snippet: Primary antibodies: polyclonal Vasa rabbit anti-mouse (1:200, NBP2-24558; Novus Biologicals), mouse monoclonal Boule (1:100, sc-166660, Santa Cruz Biotechnology, Santa Cruz, CA, USA), polyclonal acrosin rabbit anti-mouse (1:100, NBP-14260, Novus Biologicals).

    Techniques: Injection, Staining, Isolation, Cell Culture, Marker, Negative Control, Control

    Quantification of the effect of IL-1β on the percentages of developed spermatogenic cells and the expression levels of their markers in cultures from normal mice. Testicular cells were isolated from seminiferous tubules of normal immature mice and cultured in an MCS (see ) in the absence or presence of IL-1β (1, 10, and 100 pg/mL). Cultured cells were collected after 5 weeks and stained with Vasa ( A2 ), Boule ( B2 ), and acrosin ( C2 ). In addition, RNA expression levels of Vasa ( A1 ), Boule ( B1 ), and acrosin ( C1 ) were examined in these cultures by qPCR analysis using specific primers for each factor. GAPDH was used as a housekeeping gene. CT, control (without IL-1β); BC, before culture. The number of repeated experiments was (N) = 10, and the number of wells for each treatment in each experiment was (n) = 8. * compared to CT. # compared to BC. p -values: * p < 0.05, ** p < 0.01, *** p < 0.0001, ## p < 0.01, ### p < 0.001. $ p <0.05, $$$ p < 0.001.

    Journal: International Journal of Molecular Sciences

    Article Title: Effect of IL-1β on the Development of Spermatogenesis In Vitro in Normal and Busulfan-Treated Immature Mice

    doi: 10.3390/ijms25094926

    Figure Lengend Snippet: Quantification of the effect of IL-1β on the percentages of developed spermatogenic cells and the expression levels of their markers in cultures from normal mice. Testicular cells were isolated from seminiferous tubules of normal immature mice and cultured in an MCS (see ) in the absence or presence of IL-1β (1, 10, and 100 pg/mL). Cultured cells were collected after 5 weeks and stained with Vasa ( A2 ), Boule ( B2 ), and acrosin ( C2 ). In addition, RNA expression levels of Vasa ( A1 ), Boule ( B1 ), and acrosin ( C1 ) were examined in these cultures by qPCR analysis using specific primers for each factor. GAPDH was used as a housekeeping gene. CT, control (without IL-1β); BC, before culture. The number of repeated experiments was (N) = 10, and the number of wells for each treatment in each experiment was (n) = 8. * compared to CT. # compared to BC. p -values: * p < 0.05, ** p < 0.01, *** p < 0.0001, ## p < 0.01, ### p < 0.001. $ p <0.05, $$$ p < 0.001.

    Article Snippet: Primary antibodies: polyclonal Vasa rabbit anti-mouse (1:200, NBP2-24558; Novus Biologicals), mouse monoclonal Boule (1:100, sc-166660, Santa Cruz Biotechnology, Santa Cruz, CA, USA), polyclonal acrosin rabbit anti-mouse (1:100, NBP-14260, Novus Biologicals).

    Techniques: Expressing, Isolation, Cell Culture, Staining, RNA Expression, Control

    Quantification of the effect of IL-1β on the percentages of developed spermatogenic cells and the expression levels of their markers in cultures from busulfan-treated mice. Testicular cells were enzymatically isolated from seminiferous tubules of busulfan-treated immature mice and cultured in an MCS as described in . Cultured cells were collected after 5 weeks and stained with Vasa ( A2 ), Boule ( B2 ), and acrosin ( C2 ). In addition, RNA expression levels of Vasa ( A1 ), Boule ( B1 ), and acrosin ( C1 ) were examined in these cultures through qPCR analysis using specific primers for each factor. GAPDH was used as a housekeeping gene. CT, control (without IL-1β); BC, before culture. The number of repeated experiments was (N) = 4, and the number of wells for each treatment in each experiment was (n) = 8. * compared to CT. # compared to BC. p -values: ** p < 0.01, *** p < 0.0001, ### p < 0.001.

    Journal: International Journal of Molecular Sciences

    Article Title: Effect of IL-1β on the Development of Spermatogenesis In Vitro in Normal and Busulfan-Treated Immature Mice

    doi: 10.3390/ijms25094926

    Figure Lengend Snippet: Quantification of the effect of IL-1β on the percentages of developed spermatogenic cells and the expression levels of their markers in cultures from busulfan-treated mice. Testicular cells were enzymatically isolated from seminiferous tubules of busulfan-treated immature mice and cultured in an MCS as described in . Cultured cells were collected after 5 weeks and stained with Vasa ( A2 ), Boule ( B2 ), and acrosin ( C2 ). In addition, RNA expression levels of Vasa ( A1 ), Boule ( B1 ), and acrosin ( C1 ) were examined in these cultures through qPCR analysis using specific primers for each factor. GAPDH was used as a housekeeping gene. CT, control (without IL-1β); BC, before culture. The number of repeated experiments was (N) = 4, and the number of wells for each treatment in each experiment was (n) = 8. * compared to CT. # compared to BC. p -values: ** p < 0.01, *** p < 0.0001, ### p < 0.001.

    Article Snippet: Primary antibodies: polyclonal Vasa rabbit anti-mouse (1:200, NBP2-24558; Novus Biologicals), mouse monoclonal Boule (1:100, sc-166660, Santa Cruz Biotechnology, Santa Cruz, CA, USA), polyclonal acrosin rabbit anti-mouse (1:100, NBP-14260, Novus Biologicals).

    Techniques: Expressing, Isolation, Cell Culture, Staining, RNA Expression, Control

    Summary of the effect of IL-1β on the percentages of spermatogenic cells developed in vitro from cultures of cells isolated from seminiferous tubules of normal and busulfan-treated immature mice.

    Journal: International Journal of Molecular Sciences

    Article Title: Effect of IL-1β on the Development of Spermatogenesis In Vitro in Normal and Busulfan-Treated Immature Mice

    doi: 10.3390/ijms25094926

    Figure Lengend Snippet: Summary of the effect of IL-1β on the percentages of spermatogenic cells developed in vitro from cultures of cells isolated from seminiferous tubules of normal and busulfan-treated immature mice.

    Article Snippet: Primary antibodies: polyclonal Vasa rabbit anti-mouse (1:200, NBP2-24558; Novus Biologicals), mouse monoclonal Boule (1:100, sc-166660, Santa Cruz Biotechnology, Santa Cruz, CA, USA), polyclonal acrosin rabbit anti-mouse (1:100, NBP-14260, Novus Biologicals).

    Techniques: In Vitro, Isolation

    Mean value and standard deviation (StD) of the ( a ) optical density and ( b ) acrosin content of soot-free (control) and soot-treated semen after Human Acrosin ELISA Kit assays. Both figures reveal similar tendencies, but the difference between control and soot-treated samples in b is more pronounced due to a cumulative effect, since the OD-acrosin dependence is logarithmic (see ). The large StD in control specimens reflects the inherent diversity of native human ejaculates of all patients involved in the study (see ).

    Journal: Nanomaterials

    Article Title: Oxidative Stress and Acrosomal Status of Human Spermatozoa Subjected to Hydrophobic Carbon Soot Treatments

    doi: 10.3390/nano14050395

    Figure Lengend Snippet: Mean value and standard deviation (StD) of the ( a ) optical density and ( b ) acrosin content of soot-free (control) and soot-treated semen after Human Acrosin ELISA Kit assays. Both figures reveal similar tendencies, but the difference between control and soot-treated samples in b is more pronounced due to a cumulative effect, since the OD-acrosin dependence is logarithmic (see ). The large StD in control specimens reflects the inherent diversity of native human ejaculates of all patients involved in the study (see ).

    Article Snippet: MIOXSYS analytical device and Human Acrosin ELISA Kit were received from Caerus Biotech (Nyon, Switzerland) and MyBioSource (San Diego, SC, USA) respectively.

    Techniques: Standard Deviation, Control, Enzyme-linked Immunosorbent Assay