다음 MAP메이트™는 통합될 수 없습니다: -다른 분석 완충용액이 필요한 MAP메이트™. -인산 특이성 및 총 MAP메이트™ 조합, 예: 총 GSK3β 및 GSK3β(Ser 9). -PanTyr 및 자리 특이성 MAP메이트™, 예: Phospho-EGF 수용체 및 phospho-STAT1(Tyr701). -단일 표적(Akt, STAT3)를 위한 1개 이상의 1 phospho-MAP메이트™. - GAPDH 및 β-Tubulin은 panTyr를 포함하는 키트 또는 MAP메이트™와 통합될 수 없습니다.
Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
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96-Well Plate
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다른 시약 추가 (MAP메이트 사용을 위해 완충용액과 검출 키트가 필요함)
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48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
공간 절약 옵션 다수의 키트를 구매하시는 고객은 고용량 저장을 위해 키트 포장을 제거하고 비닐백에 담긴 멀티플레스 분석 구성품을 받아 저장 공간을 절약하도록 선택할 수 있습니다.
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이제 다른 키트를 사용자 지정하거나, 사전 혼합된 키트를 선택하거나, 결재하거나 또는 주문 도구를 종료할 수 있습니다.
345670
Sigma-AldrichGalanthamine, Hydrobromide - CAS 69353-21-5 - Calbiochem
A competitive and reversible inhibitor of acetylcholinesterase.
More>>A competitive and reversible inhibitor of acetylcholinesterase. Less<<
MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
A competitive and reversible inhibitor of acetylcholinesterase. Antimyasthenic agent. Can partially reverse the effects of scopolamine-induced amnesia in rats. Reported to improve learning and short-term memory in animal models.
Catalogue Number
345670
Brand Family
Calbiochem®
Synonyms
Nivalin, HBr
References
References
Pilger, C., et al. 2001. J. Mol. Graph. Model19, 288. Iliev, A., et al. 1999. Methods Find. Exp. Clin. Pharmacol. 21, 297. Southan, G.J., et al. 1996. Br. J. Pharmacol.117, 619. Mutafova-Yambolieva, V.N., et al. 1993. Gen. Pharmacol. 24, 1253.
Do not breathe dust. Wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
Product Usage Statements
Storage and Shipping Information
Ship Code
Ambient Temperature Only
Toxicity
Toxic
Hazardous Materials Attention:
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.
Storage
+2°C to +8°C
Protect from Moisture
Protect from moisture
Do not freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
카탈로그 번호
GTIN
345670-20MGCN
04055977194494
Documentation
Galanthamine, Hydrobromide - CAS 69353-21-5 - Calbiochem MSDS
Galanthamine, Hydrobromide - CAS 69353-21-5 - Calbiochem Certificates of Analysis
Title
Lot Number
345670
References
참고문헌 보기
Pilger, C., et al. 2001. J. Mol. Graph. Model19, 288. Iliev, A., et al. 1999. Methods Find. Exp. Clin. Pharmacol. 21, 297. Southan, G.J., et al. 1996. Br. J. Pharmacol.117, 619. Mutafova-Yambolieva, V.N., et al. 1993. Gen. Pharmacol. 24, 1253.
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
30-March-2010 RFH
Synonyms
Nivalin, HBr
Description
Cholinesterase antagonist. Antimyasthenic agent. Can partially reverse the effects of scopolamine-induced amnesia in rats.
Form
White solid
CAS number
69353-21-5
RTECS
DF8075000
Chemical formula
C₁₇H₂₁NO₃ · HBr
Structure formula
Purity
≥95% by HPLC
Solubility
DMSO (5 mg/ml), Ethanol (1 mg/ml) or H₂O (1 mg/ml)
Storage
Protect from moisture
+2°C to +8°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity
Toxic
Merck USA index
14, 4340
References
Pilger, C., et al. 2001. J. Mol. Graph. Model19, 288. Iliev, A., et al. 1999. Methods Find. Exp. Clin. Pharmacol. 21, 297. Southan, G.J., et al. 1996. Br. J. Pharmacol.117, 619. Mutafova-Yambolieva, V.N., et al. 1993. Gen. Pharmacol. 24, 1253.
