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    • 12. 发明申请
    • CATHETER WITH VALVE
    • 带阀的导管
    • US20120232494A1
    • 2012-09-13
    • US13412845
    • 2012-03-06
    • Takashi TanakaMotonori WatanabeMasashige Hori
    • Takashi TanakaMotonori WatanabeMasashige Hori
    • A61M25/00
    • A61M25/0075
    • A catheter with a valve is disclosed that allows smooth flow of a solution when a solution is flowing from the inside of a catheter towards the outside of a catheter and when a solution is flowing from the outside of a catheter towards the inside of a catheter. The catheter includes a tubular body 12 made of an elastic and flexible synthetic resin material and is equipped with a valve having a slit 16 passing through the outer surface 12b of the tubular body. The catheter is also provided with the movable wall 15 sunken towards the inside of the tubular body 12 at an end tip member region 14 of the tubular body 12. The location where the movable wall 15 exists has a structure with differences in hardness in the thickness direction of the tubular body 12.
    • 公开了一种具有阀的导管,当溶液从导管的内部朝向导管的外部流动并且当溶液从导管的外部朝向导管的内部流动时,允许溶液平滑流动。 导管包括由弹性和柔性的合成树脂材料制成的管状体12,并配备有具有通过管状体的外表面12b的狭缝16的阀。 导管还设置有在管状体12的端部末端构件区域14处朝向管状体12的内部凹陷的可动壁15.存在可动壁15的位置具有厚度方面的硬度差异的结构 管状体12的方向。
    • 13. 发明申请
    • MAGNETIC RECORDING MEDIUM AND MAGNETIC RECORDING AND REPRODUCING APPARATUS
    • 磁记录介质和磁记录和再现装置
    • US20120200958A1
    • 2012-08-09
    • US13502494
    • 2010-10-18
    • Takashi Tanaka
    • Takashi Tanaka
    • G11B5/33G11B5/706
    • G11B5/7325G11B5/667
    • A perpendicular magnetic recording medium of the present invention comprises a non-magnetic substrate, and at least a backing layer, an under layer, an intermediate layer and a perpendicular magnetic recording layer, which are sequentially laminated on the non-magnetic substrate, wherein the backing layer is formed of a soft magnetic film having an amorphous structure, the under layer contains a NiW alloy containing any one or both of Co and Fe, the W content of the NiW alloy is within a range from 3 to 10 atom %, the total of the Co and Fe contents of the NiW alloy is 5 atom % or more and less than 40 atom %, the saturation magnetic flux density Bs of the NiW alloy is 280 emu/cm3 or more, the thickness of the under layer is within a range from 2 to 20 nm, and the intermediate layer contains Ru or a Ru alloy.
    • 本发明的垂直磁记录介质包括依次层压在非磁性基板上的非磁性基板和至少背衬层,底层,中间层和垂直磁记录层,其中, 背衬层由具有非晶结构的软磁膜形成,底层含有含有Co和Fe中的任一种或两者的NiW合金,NiW合金的W含量在3至10原子%的范围内, NiW合金的Co和Fe含量的总和为5原子%以上且小于40原子%,NiW合金的饱和磁通密度Bs为280emu / cm 3以上,下层的厚度在 2〜20nm的范围,中间层含有Ru或Ru合金。
    • 16. 发明申请
    • MOLD FOR PRODUCING SIMULATED BLOOD VESSEL, METHOD OF PRODUCING SIMULATED BLOOD VESSEL AND SIMULATED BLOOD VESSEL
    • 用于生产模拟血液瓶的模具,生产模拟血液瓶和模拟血液容器的方法
    • US20110117531A1
    • 2011-05-19
    • US13003922
    • 2009-01-28
    • Kiyotaka IwasakiMitsuo UmezuTakashi Tanaka
    • Kiyotaka IwasakiMitsuo UmezuTakashi Tanaka
    • G09B23/30B41D3/08B29C55/22
    • G09B23/288G09B23/30
    • Disclosed is a method whereby a narrowed part similar to an actual lesioned blood vessel can be easily obtained. A mold (10) comprises first and second molded members (16, 17) having inner spaces (29, 40, 57) passing through in the axial direction and an axial member (18) detachably inserted through the individual inner spaces (29, 40, 57) of the individual molded members (16, 17). The molded members (16, 17) have tapered front parts (27, 27) respectively. In the state of facing the front ends (20) of the tapered front parts (27) to each other and thus forming a concave (12), the axial member (18) is attached. A first material (75) made of a mixed material comprising calcium carbonate or the like and silicone or the like is applied to the concave (12). A second material (76) such as silicone is applied to the entire outer periphery of the mold (10). After hardening the materials (75, 76), the mold (10) is withdrawn by detaching the axial member (18) and dividing the concave (12). Thus, a simulated blood vessel (78) having a simulated narrowed part of the blood vessel caused by calcification can be obtained.
    • 公开了可以容易地获得与实际损伤的血管类似的变窄部分的方法。 模具(10)包括具有沿轴向通过的内部空间(29,40,57)的第一和第二模制构件(16,17),以及可拆卸地插入穿过各个内部空间(29,40)的轴向构件 ,57)各个模制构件(16,17)。 模制构件(16,17)分别具有锥形前部(27,27)。 在将锥形前部(27)的前端(20)彼此面对并因此形成凹部(12)的状态下,安装轴向构件(18)。 由包含碳酸钙等的混合材料和硅树脂等制成的第一材料(75)施加到凹部(12)上。 将诸如硅树脂的第二材料(76)施加到模具(10)的整个外周。 在硬化材料(75,76)之后,通过拆卸轴向构件(18)并分开凹部(12)来撤回模具(10)。 因此,可以获得由钙化引起的具有模拟的血管狭窄部分的模拟血管(78)。
    • 19. 发明授权
    • Refrigerant cycle device and control system for vehicle
    • 车辆制冷循环装置及控制系统
    • US07836716B2
    • 2010-11-23
    • US11581441
    • 2006-10-17
    • Yoshikatsu SawadaYasutane HijikataHiromasa TanakaTakashi Tanaka
    • Yoshikatsu SawadaYasutane HijikataHiromasa TanakaTakashi Tanaka
    • F25B49/00B60H1/32
    • B60H1/3208B60H2001/3261B60H2001/3266B60H2001/3275
    • A refrigerant cycle device includes a compressor driven by a vehicle engine for drawing and compressing gas refrigerant from an evaporator, a variable displacement mechanism which varies a discharge capacity of the compressor based on a control value from an exterior to approach a suction pressure of the compressor to a predetermined suction pressure, and a control unit for controlling the discharge capacity of the compressor. The control unit includes a determining part for determining an accelerating state of the vehicle engine, a detecting member which detects a thermal load of the evaporator, a setting part for setting a minimum control value in accordance with the thermal load, and a controlling part. The controlling part reduces the control value to the minimum control value and returns the reduced control value to a control value before the reducing, when the determining means determines an accelerating state of the vehicle engine.
    • 一种制冷剂循环装置,包括:由车辆用发动机驱动的压缩机,用于从蒸发器抽取和压缩气体制冷剂;可变排量机构,其根据外部的控制值改变压缩机的排出容量,以接近压缩机的吸入压力 到预定的吸入压力,以及用于控制压缩机的排放能力的控制单元。 控制单元包括用于确定车辆发动机的加速状态的确定部件,检测蒸发器的热负荷的检测部件,用于根据热负荷设定最小控制值的设定部件和控制部件。 当确定装置确定车辆发动机的加速状态时,控制部分将控制值减小到最小控制值,并将减小的控制值返回到减小之前的控制值。
    • 20. 发明授权
    • Process for producing physiologically active protein using genetically modified silkworm
    • 使用转基因蚕生产生理活性蛋白的方法
    • US07659112B2
    • 2010-02-09
    • US10506327
    • 2003-03-06
    • Shingo HiramatsuTakashi TanakaKatsushige YamadaToshiki Tamura
    • Shingo HiramatsuTakashi TanakaKatsushige YamadaToshiki Tamura
    • C12N15/00C12P21/00
    • C12N15/8509A01K67/033A01K67/0335A01K67/04A01K2217/05A01K2267/01C07K14/52
    • The present invention provides a genetic engineering material for insects that enables a target protein to be purified easily, without requiring the use of recombinant baculovirus, while simultaneously providing a process for producing exogenous protein using that genetic engineering material. A gene recombinant silkworm is obtained by inserting an exogenous protein gene such as a cytokine gene coupled to a promoter that functions in silk glands into a silkworm chromosome. An exogenous protein such as a cytokine is then extracted and purified from the silk glands or cocoon of that silkworm or its offspring. A large amount of exogenous protein can be produced within silk gland cells, outside silk gland cells or in silk thread or a cocoon by inserting an expression gene cassette, in which the DNA sequence of the 3′ terminal portion and the DNA sequence of the 5′ terminal portion of fibroin H chain gene are fused to the exogenous protein gene, into silk gland cells and so forth.
    • 本发明提供了一种用于昆虫的遗传工程材料,其能够容易地纯化靶蛋白,而不需要使用重组杆状病毒,同时提供使用该遗传工程材料生产外源蛋白的方法。 通过将外源蛋白质基因例如与在丝腺中起作用的启动子偶联的细胞因子基因插入蚕染色体而获得基因重组蚕。 然后从蚕丝或其后代的丝腺或茧中提取和纯化外源蛋白,如细胞因子。 通过插入表达基因盒,可以在丝腺细胞,丝腺细胞外或丝线或茧中产生大量外源蛋白,其中3'末端部分的DNA序列和5'端的DNA序列 “丝心蛋白H链基因的末端部分融合到外源蛋白基因,进入丝腺细胞等。