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SERO-0120 第 20 部分 - 144 分钟SERO-0120 第 19 部分 - 138 分钟SERO-0120 第 18 部分 - 132 分钟SERO-0120 第 17 部分 - 126 分钟SERO-0120 第 16 部分 - 120 分钟SERO-0120 第 15 部分 - 114 分钟SERO-0120 第 14 部分 - 108 分钟SERO-0120 第 13 部分 - 102 分钟SERO-0120 第 12 部分 - 96 分钟SERO-0120 第 11 部分 - 90 分钟SERO-0120 第 10 部分 - 84 分钟SERO-0120 第 9 部分 - 78 分钟SERO-0120 第 8 部分 - 72 分钟SERO-0120 第 7 部分 - 66 分钟SERO-0120 第 6 部分 - 60 分钟SERO-0120 第 5 部分 - 54 分钟SERO-0120 第 4 部分 - 48 分钟SERO-0120 第 3 部分 - 42 分钟SERO-0120 第 2 部分 - 36 分钟SERO-0120 第 1 部分 - 30 分钟

SERO-0120 日本AV 提升男性持久力的有效方法与技巧。 - 免费预告片中文字幕 srt

128 分钟0 次播放


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关于 SERO-0120 日本AV视频

演员: 芦名未帆(稲森しほり), 芦名未帆(稲森しほり)

片商: EROTICA

发布日期: 3月 22日 2012年

片长: 128 分钟

字幕价格: $172.8 每分钟 1.35 美元

字幕创建时间: 5 - 9 天

类型: 审查视频

国度: 日本

语言: 日文

字幕文件类型: .srt / .ssa

字幕文件大小: <128 KB (~8960 行翻译)

字幕文件名: h_422sero00120.srt

翻译: 人工翻译(非人工智能)

人数: 2人

视频质量: 320x240, 480x360, 852x480 (SD), 1280x720 (HD), 1920x1080 (HD)

拍摄地点: 在家

发行类型: 经常出现

演戏: 动态二人组

视频代码:

版权所有者: © 2012 DMM

视频质量

1080p (HD)5,783 MB

720p (HD)3,852 MB

576p2,895 MB

432p1,934 MB

288p993 MB

144p390 MB

常问问题

如何下载完整视频?

要下载 SERO-0120 的完整视频,请向上滚动到此页面顶部并单击“下载”按钮。

然后您将被带到一个结帐页面,您可以在该页面下订单购买视频(多种分辨率可以不同的价格提供)。

这部视频没有字幕。 你能为我创建它们吗?

我们可以。

您需要做的就是为字幕下一个“自定义字幕订单”,我们将在 5 到 9 天内创建并交付字幕。

要订购 SERO-0120 的字幕,请单击此页面顶部的“订购”按钮。

自定义字幕订单如何收费?

如果尚未为视频创建字幕,您可以通过下“自定义字幕订单”请求创建字幕。

默认情况下,我们对每个AV视频标题的字幕收费为每分钟 1.50 美元的固定费率。

但是,我们确实为时长超过 90 分钟和/或包含超过 1 位女演员的电影提供折扣。 同时,由于创建字幕需要付出努力,我们对较短的电影(少于 60 分钟)收取 10% 的费用。

SERO-0120 的定制订单成本为 172.80 美元(128 分钟长视频,每分钟每分钟 1.35 美元美元)。

字幕是什么格式?

字幕采用SubRip 文件格式,这是支持最广泛的字幕格式之一。

交付时的字幕文件将命名为 h_422sero00120.srt

如何播放带字幕的视频?

您将需要一个兼容的视频播放器来播放这部视频和字幕。

为此,我们建议使用 VLC 视频播放器,因为它可以播放多种视频格式并支持字幕 .srt 和 .ass 文件格式。

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HIGH-071 a researcher is interested in the effects of a certain medication on a particular population a researcher should take a balanced approach to reduce confounding factors and ensure that the results are not biased the researcher should consider the following steps to ensure the process is unbiased these steps involve being aware of personal biases sweeping variables and following the scientific method to ensure that the study is objective this will lead to results that are scientifically and statistically valid and that are not affected by the researcher's personal opinions and personal outcomes 1 awareness of potential biases in the sampling process the researcher should take into account the different biases that might affect the sampling process including researcher and participant biases in order to conduct a valid and unbiased study the researcher should outline the methods and procedures for selecting the population participants and ensure that the targets are identified and selected without any disparities on the basis of race ethnicity or socioeconomic status this will ensure that the treatment population is representative of the target population and that the participants are representative of the wider population of the individuals being targeted 2 active role in the process of sampling and procedure the researcher should take an active role in the sampling process and the procedure of the study in order to assist with the execution and conduct of the study so that the population is representative of the target population and that the participants selected are representative of the wider population of the individuals being targeted 1 they should then clearly explain the preconditions procedure and the inclusion and exclusion criteria that would be suitable for a population sample since the inclusion criteria must be fairly sensitive to the treatment effects to be studied 3 discuss the limitations with the other staff and 5 a methodology to reduce potential variables this will assist in eventually identify and control the necessary variables that should be controlled in the study 4 allocate as appropriate the following roles and tasks to the involved clinical staff 1 the drivers and workers should be responsible for the creation of the sampling recruitments that are needed for the initial process of selecting the participants that are suitable for the study 2 the clinical and scientific staff should be responsible for the processing and interrogation of the samples that are taken out of the samples that are selected 3 supervisors and managers should oversee the overall integrity and the stratification of the trial data that are needed in the final process of making sure that the process is governed and the input is effective 5 regular de feedback conferences and reidentification should take permanent observation within the clinical trial that is conducted to ensure that the process is appropriate and that the process is managed 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22 三月 2012

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