Product Description
Lifeink® 240 is an acidic Type I collagen bioink at a concentration of 35 mg/ml for extrusion-based 3D bioprinting. The product is a highly concentrated acidified collagen solution intended to be extrusion printed employing FRESH bioprinting (see LifeSupport® Catalog No. 5244-8GM).
Lifeink® 240 produces printed structures with a high print resolution and good mechanical strength. The product is formulated in an acidic saline buffer solution. Once the collagen is printed into LifeSupport®, the pH and salts concentration of the printed structure become physiological. Cells can then be seeded onto the printed structure allowing for cell adherence and cellular remodeling of the 3D bioprinted structure.
| Parameter, Testing, and Method | Lifeink®240 #5267 |
| Sterilization Method | Filtration, Aseptic Processing |
| Sterility - USP modified | No growth |
| Form | Clear Viscous Solution |
| Package Size | 5 mL |
| Storage Temperature | 2-8°C |
| Print Temperature | 2-25°C |
| Shelf Life | Minimum of 6 months from date of receipt |
| Endotoxin - LAL | <10.0 EU/mL |
| pH | 3.0-5.0 |
Osmolality (mOsmo H2O/kg) | 450-700 |
Source Material | Bovine Collagen |
Electrophoretic Pattern - Coomassie Blue | Characteristic |
Collagen Concentration - Biuret | 30-40 mg/mL |
Collagen Purity - Silver Staining | >99% |
Continuous Flow Extrusion | Pass |
Directions for Use
Download the full PDF version or continue reading below:
Note: Employ aseptic practices to maintain the sterility of the product throughout the preparation and handling of the collagen and other solutions.
Note: Ensure that NO bubbles enter the system if mixing other materials. Bubbles in the system while mixing will turn your ink into a foam-like material.
Note: Cells should not be added directly to the Lifeink® 240 bioink since it is an acidic formulation.
Addition of other components to Lifeink®240 Bioink:
Note: Components other than cells can be added to the Lifeink® 240 bioink before bioprinting as long as these components are compatible with acidic pH conditions.
- To mix in additives to the bioink, add the additives to a secondary syringe as demonstrated in the video below:
Video for step 1
Note: The video shows cells being added to the bioink. Other materials can be added to the Lifeink® 240 bioink in lieu of cells. Cells should NOT be added directly to this bioink. For cellular bioprinting, use Lifeink® 200 #5278-5ML.
Note: For best results, add no more than 5 mL of other components per 5 mL of collagen bioink. Use a similar ratio for smaller volumes.
- Place sterile coupler on the end of the syringe with the bioink additives.
- Slowly push plunger in until solution forms a slight external meniscus above the end of the coupler on the syringe.
- Remove cap from the syringe with collagen and slowly push plunger in until collagen forms a slight external meniscus above the end of the syringe.
- Couple the syringe with additives to the syringe with collagen.(Ensure that there are no air bubbles in the system. The “external meniscus” on both syringes helps ensure that there are no air bubbles introduced).
- Slowly push plungers back and forth ~40 times to ensure thorough mixing. End with all of the material in the syringe to be used for printing.
Video for steps 2-6
- The bioink with other components is now ready for extrusion 3D bioprinters.
Note: For pneumatic printers, transfer the collagen into an appropriate syringe using the coupler. The new syringe should have the seal inserted, but the plunger removed. Centrifuge the syringe at 2000 RPM for 1 minute after transferring the collagen to remove any air bubbles.
Watch this video for help
General Printing Notes:
- To use a smaller volume of collagen, simply transfer the desired amount of collagen to another syringe, using the provided sterile coupler. To remove the air from the new syringe, you can do either of the following:
- Centrifuge the syringe (capped) with the cap pointing up to cause the air to accumulate at the cap. Evacuate the air.
- Centrifuge the syringe (capped) with the cap pointing down, and then use a hemostat to squeeze the syringe while pushing the plunger to allow the air to escape.
Removing air with a hemostat video
- When printing with FRESH gelatin slurry, allow the final printed structure to incubate at 37°C for 30 to 60 minutes and then replace the gelatin with media.
- Avoid bubbles.
For more directions on FRESH printing, please visit our LifeSupport® Directions for Use.
Product References
References for Lifeink®collagen bioinks:
Lee, A.et al.3D bioprinting of collagen to rebuild components of the human heart.Science365,482–487 (2019).
Maxson, Eva L., et al. "In vivo remodeling of a 3D-Bioprinted tissue engineered heart valve scaffold."Bioprinting(2019): e00059.
Filardo, G.et al.Patient-specific meniscus prototype based on 3D bioprinting of human cell-laden scaffold.Bone & Joint Research8,101–106 (2019).
Schmitt, T. Analysis and Classification of 3-D Printed Collagen-Bioglass Matrices for Cellular Growth Utilizing Artificial Neural Networks.University Thesis (2018).
Balakhovsky, Y. M., Ostrovskiy, A. Y. & Khesuani, Y. D. Emerging Business Models Toward Commercialization of Bioprinting Technology.3D Printing and Biofabrication1–22 (2017). doi:10.1007/978-3-319-40498-1_25-1
Fox, S.et al.A simplified fabrication technique for cellularized high-collagen dermal equivalents.Biomedical Materials14,041001 (2019).
Product Certificate of Analysis
Safety and Documentation
Safety Data Sheet
Certificate of Origin
Declaration of Material Source
Product Disclaimer
This product is for R&D use only and is not intended for human or other uses. Please consult the Material Safety Data Sheet for information regarding hazards and safe handling practices.
美国AdvancedBioMatrix(简称ABM) www.advancedbiomatrix.comAdvancedBioMatrix(简称ABM)是美国一家著名的生物公司,获得了AllerganInc的授权(Allergan用25年时间不断完善胶原蛋白相关的产品的生产工艺),将Allergan的专业和技术用于蛋白生产与检测,致力于为组织工程、细胞分析及细胞增殖等研究领域提供优质稳定的产品。AdvancedBioMatrix不断丰富已有产品线,目前可为三维细胞培养提供各种胶原蛋白、纤连蛋白、玻连蛋白、水性凝胶、不同粘度与分子量的透明质酸以及低代成纤维细胞等。在美国全部产品授权Sigma销售。AdvancedBioMatrix是组织培养,细胞分析和细胞增殖三维(3D)应用的生命科学领域的领导者。我们的产品被公认为纯度,功能性和一致性的标准。我们在生产,分离,纯化,冷冻干燥,细胞培养和蛋白质测试,粘附肽,附着因子,底物刚性和其他3D矩阵产品方面拥有丰富的专业知识。我们的专业技术和知识正在被用来确保我们的产品质量最高,批次之间一致且易于为我们的研究客户使用。
美国AdvancedBioMatrix是3D组织培养、细胞检测和细胞增殖等领域实验解决方案的佼佼者。AdvancedBioMatrix在分离、纯化、冻干、细胞培养和蛋白检测、多肽粘附、附着因子、基质硬度和其他3Dmatrix 产品开发方面有着丰富的经验。AdvancedBioMatrix的研发经验和专业知识确保其产品可达到最佳质量,并保证产品之间一致性,方便研究客户使用。以下为AdvancedBioMatrix3DMatrices 产品竞争优势:1. 提供高纯度和成分确定的胞外基质;2. 超过1000余篇文献引用PureCol产品,品质非常均一;3. 在3D培养基领域可提供最全面的产品线;4. 唯一可提供特异性刚性有机硅基板的公司(CytoSoft);5. 唯一可提供可溶性丝纤蛋白的供应商(可运用于多种3D培养);6. 如果客户首次接触3D胶原凝胶,AdvancedBioMatrix还是唯一的预制胶原蛋白(PureColEZGel)供应商;
以下产品为AdvancedBioMatrix全球畅销品:1.PureCol 牛源I型胶原蛋白 3mg/ml#5005-100ML2.Nutragen牛源I型胶原蛋白 6mg/ml#5010-50ML3.FibriCol 牛源I型胶原蛋白 10mg/ml#5133-20ML4.VitroCol 人源I型胶原蛋白 #5007-20ML5. 弹性蛋白原 #5052-1MG6.ECMSelectArraykitUltra-36#5170-1EA7.CytoSoft(刚性可变的基底,AdvancedBioMatrix最新添加产品5190-7EA)8. 人III型胶原蛋白 #5021-10MG9. 人IV型胶原蛋白 #5022-5MG10.SilkFibroin溶液 #5154-20ML11.Fibronectin#5080-5MG12.Vitronectin#5051-0.1MG
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问题:
1,既然外国公司的原材料这么贵,我就想购买国内厂家的,请各位大侠帮忙提供一下国内哪些厂家的玻璃胚针物廉价美?
2,国内的哪些大学的测试中心,能够提供拉针仪的有偿使用服务的?
具体操作是:局麻下将3~4根电极导管经股静脉、锁骨下静脉送入冠状静脉窦、高位右心房及希氏束、右心室等部位,刺激心房和心室诱发与临床一致的心动过速,定位心动过速起源点,然后将消融用的电极导管送达已定位的起源点并与体外的射频发生器相连。放电后重复电生理检查,若不能诱发心动过速且临床随访无发作,则说明消融成功。
此方法治疗的疾病有:预激综合征和房室结双经路引起的阵发性室上性心动过速、房扑和房颤、室性心动过速及房性心动过速。
脑电波:
脑电波(Electroencephalogram,EEG)是大脑在活动时,大量神经元同步发生的突触后电位经总和后形成的。它记录大脑活动时的电波变化,是脑神经细胞的电生理活动在大脑皮层或头皮表面的总体反映。
脑电波来源于锥体细胞顶端树突的突触后电位。脑电波同步节律的形成还与皮层丘脑非特异性投射系统的活动有关。
脑电波是脑科学的基础理论研究,脑电波监测广泛运用于其临床实践应用中。
电子波
电子波是指电子产品等所发出的电子辐
电子波的害处
电脑及大多数家用电器设备等都是可以产生各种形式不同频率、不同强度的电磁辐射源。
电磁辐射--对人体机理的危害
电场辐射危害人体的机理主要是热效应、非热效应和累积效应等。
热效应:人体70%以上是水,水分子受到电子波辐射后相互摩擦,引起机体升温,从而影响到体内器官的正常工作。
非热效应:人体的器官和组织都存在微弱的电磁场,它们是稳定和有序的,一旦受到外界电场的干扰,处于平衡状态的微弱电场即将遭到破坏,人体也会遭受损伤。
累积效应:热效应和非热效应作用于人体后,对人体的伤害尚未来得及自我修复之前(通常所说的人体承受力---内抗力),再次受到电子波辐射的话,其伤害程度就会发生累积,久之会成为永久性病态,危及生命。对于长期接触电子波辐射的群体,即使功率很小,频率很低,也能诱发体内想不到的病变,应引起警惕。
谢谢啦~
1.在没有开始记录(空跑的状态下)和开始记录时的波形的基线都不在0点而是处于负值,是因为仪器设备设置的问题还是仪器本身有损坏?
2.记录ACC场电的通道50Hz干扰特别大,接地线排干扰后仍然存在,可能是什么问题呢?
3.Brownlee440的Amplifier上有Gain,lowpassfilter,Highpassfilter的设置,这个设置对ACC场电的记录有影响吗?如果记录ACC的场电,一般常用的参数是多少啊?
4.有没有用过这个仪器记录过肌电的前辈,我用A-B模式可以记录到类似Chart5软件记录的肌电波形。可是用clampfit10.2的Analyze--statistics--Measurement--Area分析,分析出来的数值太小,与波形不符。从波形看,明显有强的肌肉收缩,但是数值却没有明显差异。有前辈分析过肌电吗?是否我的分析方法不对?或者是应为问题1中提到的基线不在0点所引起的曲线下面积分析的误差?
感谢!

