475818
Microcystin-LW, Microcystis aeruginosa
Analog of Microcystin-LR with Trp substituted in place of Arg. Believed to be more cell-permeable than other microcystins making it useful for biochemical studies in intact cells.
别名:
Microcystin-LW, Microcystis aeruginosa, MCYST-LW
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About This Item
经验公式（希尔记法）:
C54H72N8O12
分子量:
1025.20
分類程式碼代碼:
12352200
NACRES:
NA.77
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品質等級
化驗
≥95% (HPLC)
形狀
film
製造商／商標名
Calbiochem®
儲存條件
OK to freeze
顏色
colorless
溶解度
methanol: 2 mg/mL
DMSO: 2.5 mg/mL
運輸包裝
ambient
儲存溫度
−20°C
一般說明
Analog of Microcystin-LR (Cat. No 475815) with Trp group substituted in place of Arg. Believed to be more cell-permeable than other microcystins, making it useful for biochemical studies in intact cells.
Analog of Microcystin-LR (Cat. No. 475815) with Trp substituted in place of Arg. Believed to be more cell-permeable than other microcystins making it useful for biochemical studies in intact cells.
生化／生理作用
Cell permeable: yes
Product does not compete with ATP.
Reversible: no
包裝
yes
警告
Toxicity: Highly Toxic (H)
其他說明
Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
法律資訊
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
L A Lawton et al.
The Analyst, 119(7), 1525-1530 (1994-07-01)
Increasing concern over the presence of microcystins (cyanobacterial/blue-green algal hepatotoxins) in water supplies has emphasized the need for a suitable analytical method. As many microcystins are known to exist, a method was developed that permits the determination of numerous variants
L A Lawton et al.
Natural toxins, 3(1), 50-57 (1995-01-01)
Six microcystins were identified in a laboratory culture of the cyanobacterium (blue-green alga) Microcystis aeruginosa PCC 7813 using high-performance liquid chromatography coupled with diode array detection (HPLC-DAD) and mass spectrometry (LC-MS). The toxins were purified and further characterized by amino
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