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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 保质期:
一年以上
- 英文名:
Collagenase, Type I, powder
- 库存:
现货
- 供应商:
北京智杰方远
- CAS号:
******
- 保存条件:
2°C - 8°C
- 规格:
1g
产品简介
胶原酶I 美国GIBCO (价格优惠)Prepared from Clostridium histolyticum for dissociation of tissues.Suggested for epithelial, lung, fat, and adrenal tissue cell preparations.
产品详细信息
| 胶原酶I | GIBCO[17100-017] | 100mg |
| GIBCO原装[17100-017] | 1g |
Collagenase
Cat. No.: 17100 Type I
17101 Type II
17102 Type III
17103 Hepatocyte Qualified
17104 Type IV
Sizes: See catalog.
Custom pack sizes available upon request.
Storage: 2 to 8°C (-5 to -20°C after reconstitution)
Avoid moisture and exposure to light.
Avoid inhalation and skin contact.
This product is intended for cell or tissue disaggregation only.
Background
Collagenase (from clostridium histolyticum) is a protease with a specificity for the bond between a
neutral amino acid (x) and glycine in the sequence Pro-X-Glyc-Pro. This sequence is found in high
frequency in collagen and is unique among proteases in its ability to degrade the triplehelical native
collagen fibrils commonly found in connective tissue.
The collagenase most commonly used for tissue dissociation is a crude preparation containing
clostripiopeptidase A and a number of other proteases, polysaccharidases and lipases. This crude
enzyme is ideally suited for tissue dissociation since it contains the enzyme required to attack
native collagen and reticular fibers, in addition to the enzymes which hydrolyze the other proteins,
polysaccharides and lipids in the extracellular matrix of connective and epithelial tissues.
Crude collagenase does exhibit lot-to-lot variability and may produce occasional toxicity. Invitrogen
attempted to minimize these difficulties by tissue-typing their crude collagenase lots based upon a
correlation between various enzyme levels in each preparation and effectiveness in dissociating
certain tissues.
Specifications
Potency: One unit liberates 1 μM of L-leucine equivalents from collagen in 5 hours at +37°C,
pH 7.5.
Types: Particular enzymatic activities of crude collagenases have correlated with the
tissues from which the cells were obtained (or with the uses to which the cells are
put), and as a result of the correlation’s, several formal types have been established.
Type III Selected because of low proteolytic activity. (casein as substrate)
Type IV Selected because of low tryptic activity. (BAEE as substrate)
These selected types have been found to give better performance in preparation of cells from
the various tissues as tabulated below. It should be noted, however, that while the results
have been greatly improved following this classification, there is still some lot-to-lot variation,
and efforts continue in attempting to gain even better control over crude collagenase.
TYPE TISSUES OR CELLS
I Fat cells, Adrenal, Liver
II Heart, Bone, Thyroid, Cartilage, Liver
III Mammary
IV Islet (insulin receptor sites)
Inhibitors: Metal chelating agents such as cysteine, EDTA or o-phenanthroline but not
DFP. It is also inhibited by a2-macroglobulin, a large plasma glycoprotein.
Instructions for use
A. Preparing stock and working solution
Dissolve the non-sterile, lyophilized enzyme in HBSS (Cat. No. 14025). Filter sterilize the
solution with a cell culture approved filtration unit. Crude collagenase is most often used
in concentrations from 0.1 to 0.5% (W/V) or 50 to 100 U/mL. Once reconstituted use
immediately or store frozen. Thaw in refrigerator immediately prior to use.
B. Dissociation of tissue
• Tissue is minced with a sterile scalpel or scissors.
• Wash the tissue several times in HBSS.
• The tissue fragments are soaked at +37°C. Increased efficiency is obtained using a
rocker platform and supplementing the digest with 3 mM CaCl2.
C. Organ perfusion
• Digest is prewarmed to +37°C and perfused at a rate preoptimized for the particular
organ. Addition of 3 mM CaCl2 increases the efficiency of dissociation.
• Dispersed cells and tissue fragments are separated from larger pieces by passing the
mixture through a sterile stainless steel or nylon mesh. Fresh collagenase solution
can be added to the fragments if further disaggregation is required.
• Wash several times to eliminate debris and enzyme solution. A density separation
step (Nycodenz) will give a cleaner suspension.
• Resuspend the pellet in the culture medium and incubate under predetermined
conditions.
For further information on this or other GIBCOTM products, contact Technical Services at the
following:
United States TECH-LINE SM : 1 800 955 6288
Canada TECH-LINE: 1 800 757 8257
Outside the U.S. and Canada, refer to the GIBCO products catalogue for the TECH-LINE in your
region.
You may also contact your Invitrogen Sales Representative or our World Wide Web site at
www.invitrogen.com.
For research use only.
CAUTION: Not intended for human or animal
diagnostic or therapeutic uses.
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文献和实验胶原酶I Gibco 17100017 100mg 220 胶原酶II Gibco 17101015 100mg 220 胶原酶IV Gibco 17104019 100mg 220 链脲佐菌素 Sigma S0130 100mg 198 牛血清白蛋白 Amresco 332 5g 40 分子生物学 RNAout(快速RNA提取试剂) 国产 50次 329 Erasol(RNA酶清除剂) 国产 50ml 112 Taq
内皮细胞分布于整个循环系统,从心脏到最小的毛细血管。在这个步骤中,气管的活力很非常重要。取出器官和开始消化之间的时间越短将提高细胞更有活力的产出及不在含氧量低的条件下太久。小鼠的数量需要:小鼠应该是5~6周大小。年龄大的小鼠内皮细胞的产出会少些。最少5个小鼠可以得到很好的产出。 一、材料和试剂 1. 内皮细胞生长添加剂(ECGS)(Sigma,catalognumber:E2759) 2. 胶原酶I(Invitrogen,Catalognumber:17100-017
%酒精中浸泡. 在超净平台中解剖进减少污染。 2. 去除内膜使用的镊子即可. 来回刮. 除去内皮细胞。 3. 去除内皮和外膜后. 置于20%FBS的D ME M培养液中2-3天. 得到更多的细胞。 4. 在0. 2%胶原酶I中消化时. 应经常地摇动. 有利于消化. 又可以仔细观察. 一举二得啊 5. 动脉消化后. 会有一些脱落的细胞和丝状或是一小块. 可以分开来养. 一个贴于培养皿中
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