Thermo Fisher Scientific Tramadol Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA175471 | - | Thermo Fisher Scientific PA175471 Tramadol Polyclonal Antibody 1 mg pk | 재고문의 | pk | 1,163,000원 | - | 1,279,300원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
ELISA (ELISA)
5-10 µg/mL
Product Specifications
Species Reactivity
Chemical
Host/Isotype
Sheep / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Tramadol(N)-BTG
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Purification
purified
Storage buffer
PBS, pH 7.4
Contains
0.09% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_1091010
Product Specific Information
Working Concentration: 5 µg/mL. Sensitivity: 10 ng/mL Tramadol produces 96% inhibition in a competitive ELISA employing Tramadol polyclonal antibody.
Target Information
Tramadol is only found in individuals that have used or taken this drug. It is a narcotic analgesic proposed for moderate to severe pain. It may be habituating. [PubChem] Tramadol and its O-desmethyl metabolite (M1) are selective, weak OP3-receptor agonists. Opiate receptors are coupled with G-protein receptors and function as both positive and negative regulators of synaptic transmission via G-proteins that activate effector proteins. As the effector system is adenylate cyclase and cAMP located at the inner surface of the plasma membrane, opioids decrease intracellular cAMP by inhibiting adenylate cyclase. Subsequently, the release of nociceptive neurotransmitters such as substance P, GABA, dopamine, acetylcholine and noradrenaline is inhibited. The analgesic properties of Tramadol can be attributed to norepinephrine and serotonin reuptake blockade in the CNS, which inhibits pain transmission in the spinal cord. The (+) enantiomer has higher affinity for the OP3 receptor and preferentially inhibits serotonin uptake and enhances serotonin release. The (-) enantiomer preferentially inhibits norepinephrine reuptake by stimulating alpha(2)-adrenergic receptors. [National Center for Biotechnology Information. PubChem Compound Database; CID=33741].
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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