- ￥2980
- LSM Bio
- 78-5000pg/ml
- 39pg/ml
- 进口
- ELI-14588m
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
50
- 供应商：
LSM BIO
- 检测范围：
78-5000pg/ml
- 检测方法：
夹心法ELISA或竞争法ELISA
- 应用：
检测小鼠血清，血浆，组织匀浆内的目标蛋白含量
- 适应物种：
小鼠
- 标记物：
ProSAAS, Pcsk1n
- 样本：
小鼠血清，血浆，组织匀浆
- 灵敏度：
39pg/ml
- 规格：
96Tests
Mouse ProSAAS, PCSK1N ELISA Kit
FOR RESEARCH USE ONLY!
96 Tests
Alternative name
Mouse PCSK1N ELISA KIT ,Mouse granin like neuroendocrine peptide precursor ELISA KIT ,Mouse PROSAAS ELISA KIT ,Mouse SAAS ELISA KIT ,Mouse SCG8 ELISA KIT ,Mouse SgVIII ELISA KIT ,Mouse granin-like neuroendocrine peptide ELISA KIT ,Mouse pro-SAAS ELISA KIT ,Mouse proprotein convertase 1 inhibitor ELISA KIT ,Mouse proprotein convertase subtilisin/kexin type 1 inhibitor ELISA KIT
Intended use
Mouse PCSK1N ELISA kit allows for the in vitro quantitative determination of Mouse ProSAAS concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.
Mouse PCSK1N ELISA kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to PCSK1N, During the reaction, PCSK1N in the sample or standard competes with a fixed amount of biotin-labeled PCSK1N for sites on a pre-coated Monoclonal antibody specific to PCSK1N. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of PCSK1N in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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文献和实验Clinical Chemistry and Other Laboratory Tests on Mouse Plasma or Serum
Materials Lyophilized rat/mouse PINP calibrators 0 to 5 and controls 1 and 2 (from Competitive ELISA kit; IDS Ltd, http://www.idsplc.com/): reconstitute calibrators
Performing Bronchoalveolar Lavage in the Mouse
and inflammatory cell populations; it is indispensable for studying cell influx in disease models of the airways such as asthma and COPD. Cell counts can be combined with methods such as ELISA, immunoblot, immunohistochemistry, quantitative polymerase chain
Detection of apoptotic process in situ using immunocytochemical and TUNEL assays
from invertebrates to lower and higher verterbrates, and intervenes both in physiological and in pathological states, such as normal cell turnover, embryogenesis, metamorphosis, thymic maturation and involution, neoplasm, etc. (1-4). A mouse anti-DNA monoclonal
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