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.
Catalogue Number
Ordering Description
Qty/Pack
List
이 제품은 즐겨찾기에 저장되었습니다.
종
패널 유형
선택하신 키트
수량
카탈로그 번호
주문 설명
포장 단위
기재 가격
96-Well Plate
수량
카탈로그 번호
주문 설명
포장 단위
기재 가격
다른 시약 추가 (MAP메이트 사용을 위해 완충용액과 검출 키트가 필요함)
수량
카탈로그 번호
주문 설명
포장 단위
기재 가격
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.
이 제품은 즐겨찾기에 저장되었습니다.
해당 제품은 고객님의 카트에 추가되었습니다.
이제 다른 키트를 사용자 지정하거나, 사전 혼합된 키트를 선택하거나, 결재하거나 또는 주문 도구를 종료할 수 있습니다.
Many molecules absorb in the ultraviolet (UV) and visible (Vis) range of the electromagnetic spectrum. UV radiation covers the range from 190-350 nm, while visible radiation covers the 350-800 nm range. The absorption of radiation corresponds to the excitation of outer electrons in the molecule. In a spectrophotometer, radiation with a specific intensity is passed through a liquid sample that is contained in a cuvette (usually made of quartz). If the sample contains species that absorb(s) in that specific radiation wavelength, the radiation intensity emerging on the other side of the cuvette is reduced. This phenomenon is used to identify and/or quantify a molecule in a sample. Compounds have unique UV-Vis spectra, including a maximum absorption wavelength (λmax) and molar extinction coefficient (ε), so UV-Vis can be used to identify the presence of chemicals in samples. Because of this, UV-Vis is a popular technique in chemistry, foods, pigments, pharmaceuticals, polymers, and the life sciences, for basic or applied research as well as quality control.
Quantitation in UV-Vis spectrophotometry is expressed by Beer-Lambert’s Law:
Aλ = ελ c l
where Aλ = absorbance at wavelength λ, ελ = extinction coefficient at wavelength λ, c = concentration, and l = pathlength. In most experiments, ε and l are constant, therefore absorbance is proportional to the concentration of the compound.
UV-Vis spectrophotometers can be either single beam or double beam in design. In single-beam instruments, all the light passes through the sample cell, therefore a correction for the loss of light intensity as the beam passes through the solvent must be made. This is done by replacing the sample by a blank or reference sample to account for any matrix effects. Dual-beam spectrophotometers split the light into two beams before it reaches the sample. One beam is used as a reference beam, and the other passes through the sample. Correction is performed automatically.
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