- $875
- LSBio
- 62.5 - 4000 pg/ml
- LS-F29823
- 美国
- 2025年07月16日
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- 详细信息
- 文献和实验
- 技术资料
- 样本：
血清/血浆/组织匀浆液
- 库存：
1000
- 适应物种：
Human
- 应用：
科研使用
- 检测方法：
ELISA
- 检测范围：
62.5 - 4000 pg/ml
- 供应商：
康朗生物
- 规格：
96T
Human IgA, Secretory ELISA Kit (CLIA)
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Product Description
LS-F29823 is a 96-well enzyme-linked immunosorbent assay (ELISA) for the Quantitative detection of Human IgA, Secretory in samples of Plasma and Serum. It is based upon a Sandwich CLIA assay principle and can be used to detect levels of IgA, Secretory as low as 37.5 picograms per milliliter.Specifications
TypeCLIA (chemiluminescent immunoassay) kit
Target
IgA, Secretory
Reactivity
Human
Manual
Intended Sample Types
Plasma, Serum
Format
12 x 8-Well Microstrips
Detection
Chemiluminescent
Measurement
Quantitative
Detection Range
62.5 - 4000 pg/ml
Sensitivity
37.5 pg/ml
Precision
Intra-Assay: CV<15% Inter-Assay: CV<15%
Storage
Short term: 4°C; Long term: see manual.
Quality Assurance
Due to their limited shelf life, LSBio ELISA kits are not typically stocked as finished goods. Upon receipt of an order each kit is assembled and tested to ensure that it meets specifications before shipping. Minor changes may occur to the Range, Sensitivity, and Precision. In the event of a significant change the order would be confirmed with the customer before shipping ELISA kit lot numbers reflect the date of final assembly and testing for each specific kit rather than a bulk manufactured lot. All kits are tested to confirm that they fall within their defined Inter- and Intra- assay coefficient of variation.
Kit Components
- User Manual
- 96-well Microplate
- Detection Reagents
- Wash Buffer
- Substrate
- Stop Solution
- Adhesive Plate Sealers
Restrictions
For research use only.
Guarantee
This elisa kit carries the LSBio 100% Guarantee.
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Sandwich CLIA Platform Overview
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文献和实验Purification and Characterization of Human Serum and Secretory IgA1 and IgA2 Using Jacalin
Human immunoglobulin A (IgA) is found in serum and secretions in several different forms (1 ), Serum IgA is produced by the bone marrow and is pre-dominately monomeric (M r = 160 kDa
for the serodiagnosis of human fasciolosis. The methods illustrated in this chapter will explain the isolation of cysteine proteases from F. hepatica excretory-secretory products by gel filtration and anion exchange chromatography, and their subsequent characterization
Synchronizing Protein Transport in the Secretory Pathway
or transported to their target compartments, newly synthesized proteins leave the endoplasmic reticulum to reach the Golgi apparatus, where they are processed and sorted toward their final destinations along the secretory pathway. It is now clear that many Golgi
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