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Hamilton Thorne Ltd computer aided sperm analysis system casa
Computer Aided Sperm Analysis System Casa, supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
computer aided sperm analysis system casa - by Bioz Stars, 2026-05
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Hamilton Thorne Ltd computer aided sperm analysis system casa
Computer Aided Sperm Analysis System Casa, supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/computer aided sperm analysis system casa/product/Hamilton Thorne Ltd
Average 86 stars, based on 1 article reviews
computer aided sperm analysis system casa - by Bioz Stars, 2026-05
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Hamilton Thorne Ltd computer aided sperm analysis casa
( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Computer Aided Sperm Analysis Casa, supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/computer aided sperm analysis casa/product/Hamilton Thorne Ltd
Average 86 stars, based on 1 article reviews
computer aided sperm analysis casa - by Bioz Stars, 2026-05
86/100 stars
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Hamilton Thorne Ltd computer aided sperm analysis casa system
( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Computer Aided Sperm Analysis Casa System, supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/computer aided sperm analysis casa system/product/Hamilton Thorne Ltd
Average 86 stars, based on 1 article reviews
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( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Casa (Computer Aided Sperm Analysis), supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Computer Aided Sperm Analysis (Casa) Program Ht Casaceros Ii, supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Microptic SL sperm class analyzer (sca®) computer-aided sperm analysis (casa) system
( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Sperm Class Analyzer (Sca®) Computer Aided Sperm Analysis (Casa) System, supplied by Microptic SL, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Computer Aided Sperm Analysis (Casa; Sca® System), supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/computer-aided sperm analysis (casa; sca® system)/product/Hamilton Thorne Ltd
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( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Computer Aided Sperm Analysis Casa, supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/computer-aided sperm analysis casa/product/Hamilton Thorne Ltd
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( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a <t>CASA</t> system to identify the percentage of <t>motile</t> <t>spermatozoa</t> ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.
Computer Aided Sperm Analysis System Casa, supplied by Hamilton Thorne Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/computer-aided sperm analysis system casa/product/Hamilton Thorne Ltd
Average 90 stars, based on 1 article reviews
computer-aided sperm analysis system casa - by Bioz Stars, 2026-05
90/100 stars
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( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a CASA system to identify the percentage of motile spermatozoa ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.

Journal: eLife

Article Title: Sperm motility in mice with oligo-astheno-teratozoospermia restored by in vivo injection and electroporation of naked mRNA

doi: 10.7554/eLife.94514

Figure Lengend Snippet: ( A ) Adult Armc2 KO mouse testes were injected with a solution containing Armc2 -mRNA. After injection, the testes were electroporated. At different times (3-, 6-, 10-, 15-, 21-, 28-, and 35-day post -injection), sperm were extracted from the cauda epididymis of the injected testis, and the sample was then examined with a CASA system to identify the percentage of motile spermatozoa ( A1 ). n = 2 for day 15, n = 3 for days 3, 6, and 21, n = 4 for day 10, and n = 5 for days 28 and 35. ( A2 ) Sperm motility parameters of Armc2 −/− -rescued sperm in comparison to Armc2 +/+ sperm. The motility parameters measured were: averaged path velocity (VAP); straight line velocity (VSL); curvilinear velocity (VCL); amplitude of lateral head displacement (ALH); beat cross frequency (BCF); straightness (STR); linearity (LIN). Black dots: sperm cells from Armc2 null mice, green dots: sperm cells from Armc2 null mice 35 days after injection with Armc2 -mRNA. Results are expressed as mean ± SD. ( A3 ) Sperm motility population of Armc2 −/− -rescued sperm in comparison to Armc2 −/− sperm. Black column: sperm cells from Armc2 null mice, green column: sperm cells from Armc2 null mice 35 days after injection with ARmc2 -mRNA. Statistical significance was verified using a Mann–Whitney sum test. Data are displayed as mean ± SEM. p values of *≤0.05, **≤0.01, or ***≤0.001 were considered to represent statistically significant differences. ( B ) Morphology of sperm cells in Armc2 KO mice injected or not with Armc2 -mRNA. ( B1, B2 ) Microscopic observation of epididymal sperm cells from a mature WT mouse. ( B3, B4 ) Epididymal sperm cells from a mature Armc2 KO mouse 35 days after injection/electroporation with Armc2 -mRNA. ( B5, B6 ) Epididymal sperm cells from a control Armc2 KO male. Normal sperm cells were observed in the injected condition with Armc2 -mRNA (white arrows). Scale bars: 10 µm.

Article Snippet: Motility of the spermatozoa was evaluated at 37°C with an Olympus microscope and Computer Aided Sperm Analysis (CASA) (CEROS II apparatus; Hamilton Thorne, Beverley, MA, USA).

Techniques: Injection, Comparison, MANN-WHITNEY, Electroporation, Control