Cardiotoxin Analog (CTX) IV 6-12
(Synonyms: 心脏毒素类似物多肽) 目录号 : GC35609Cardiotoxin Analog (CTX) IV 6-12是环磷酰胺类似物(CTX)IV的一部分肽,来源于Naja atra(台湾眼镜蛇)的毒液,是一种独特的心脏毒素类似物。
Cas No.:115722-23-1
Sample solution is provided at 25 µL, 10mM.
Cardiotoxin Analog (CTX) IV 6-12 is a peptide fragment of cyclophosphamide analog (CTX) IV, derived from the venom of Naja atra, and is a unique cardiotoxin analog[1]. Cardiotoxin Analog (CTX) IV 6-12 has a three-finger ring structure similar to neurotoxins and muscarinic toxins and has cytolytic effects on many cells[2]. Cardiotoxin Analog (CTX) IV 6-12 can cause depolarization and contraction of smooth and skeletal muscles, as well as depolarization of nerve cells[3]. Cardiotoxin Analog (CTX) IV 6-12 is able to induce membrane fusion of vesicles formed by phospholipids such as cardiolipin or sphingomyelin[4]. Cardiotoxin Analog (CTX) IV 6-12 is the only cardiotoxin isoform known to date that has a positively charged residue at the N-terminal amino acid[5]. CTX IV differs from CTX II only by the presence of arginine in place of a leucine residue at position 1[6].
References:
[1] Kaneda N, Sasaki T, Hayashi K. Primary structures of cardiotoxin analogues II and IV from the venom of Naja naja atra[J]. Biochimica et Biophysica Acta (BBA)-Protein Structure, 1977, 491(1): 53-66.
[2] Wu W G. Diversity of cobra cardiotoxin[J]. Journal of Toxicology: Toxin Reviews, 1997, 16(3): 115-134.
[3] Harvey A L. Cardiotoxins from cobra venoms: possible mechanisms of action[J]. Journal of Toxicology: Toxin Reviews, 1985, 4(1): 41-69.
[4] Forouhar F, Huang W N, Liu J H, et al. Structural basis of membrane-induced cardiotoxin A3 oligomerization[J]. Journal of Biological Chemistry, 2003, 278(24): 21980-21988.
[5] Jang J Y, Kumar T K S, Jayaraman G, et al. Comparison of the hemolytic activity and solution structures of two snake venom cardiotoxin analogues which only differ in their N-terminal amino acid[J]. Biochemistry, 1997, 36(48): 14635-14641.
[6] Kumar T K S, Pandian S T K, Jayaraman G, et al. Understanding the structure, function and folding of cobra toxins[J]. PROCEEDINGS-NATIONAL SCIENCE COUNCIL REPUBLIC OF CHINA PART A PHYSICAL SCIENCE AND ENGINEERING, 1999, 23: 1-19.
Cardiotoxin Analog (CTX) IV 6-12是环磷酰胺类似物(CTX)IV的一部分肽,来源于Naja atra(台湾眼镜蛇)的毒液,是一种独特的心脏毒素类似物[1]。Cardiotoxin Analog (CTX) IV 6-12具有类似于神经毒素和毒蕈碱毒素的三指环结构,对许多细胞具有溶细胞作用[2]。Cardiotoxin Analog (CTX) IV 6-12能够引起平滑肌和骨骼肌的去极化和挛缩,以及神经细胞的去极化[3]。Cardiotoxin Analog (CTX) IV 6-12能够诱导由磷脂(例如心磷脂或鞘磷脂)形成的囊泡的膜融合[4]。Cardiotoxin Analog (CTX) IV 6-12是迄今为止已知的唯一在N-末端氨基酸处具有带正电荷残基的心脏毒素同种型[5]。CTX IV与CTX II的唯一区别是,第1位上的亮氨酸残基被精氨酸取代[6]。
Cas No. | 115722-23-1 | SDF | |
别名 | 心脏毒素类似物多肽 | ||
分子式 | C48H70N10O7 | 分子量 | 899.13 |
溶解度 | 100 mg/ml in water | 储存条件 | Store at -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
||
Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 1.1122 mL | 5.5609 mL | 11.1219 mL |
5 mM | 0.2224 mL | 1.1122 mL | 2.2244 mL |
10 mM | 0.1112 mL | 0.5561 mL | 1.1122 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet