ARG83497

Monkey CST3 / Cystatin C ELISA Kit

Monkey CST3 / Cystatin C ELISA Kit for ELISA and Monkey

Overview

Product Description ARG83497 Monkey CST3 / Cystatin C ELISA Kit is an Enzyme Immunoassay kit for the quantification of Monkey CST3 / Cystatin C in Plasma and Serum
Tested Reactivity Mk
Tested Application ELISA
Target Name CST3 / Cystatin C
Conjugation HRP
Conjugation Note Substrate: TMB and read at 450 nm.
Sensitivity 0.0625 ng/ml
Sample Type Plasma and Serum
Standard Range 0.125 - 4 ng/ml
Sample Volume 100 μl
Precision Intra-Assay CV: < 10%
Inter-Assay CV: < 10%
Alternate Names CST3; Cystatin C; Neuroendocrine Basic Polypeptide; Post-Gamma-Globulin; Gamma-Trace; Cystatin-C; Cystatin C (Amyloid Angiopathy And Cerebral Hemorrhage); Epididymis Secretory Protein Li 2; BA218C14.4 (Cystatin C); Cystatin 3; Cystatin-3; HEL-S-2; ARMD11

Application Instructions

Assay Time 2 hours

Properties

Form 96 well
Storage Instruction Store the kit at 4°C. Keep microplate wells sealed in a dry bag with desiccants. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 574313 Monkey CST3

Swiss-port # O19092 Monkey Cystatin-C

Gene Symbol CST3
Gene Full Name cystatin C
Background The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions, where they appear to provide protective functions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes the most abundant extracellular inhibitor of cysteine proteases, which is found in high concentrations in biological fluids and is expressed in virtually all organs of the body. A mutation in this gene has been associated with amyloid angiopathy. Expression of this protein in vascular wall smooth muscle cells is severely reduced in both atherosclerotic and aneurysmal aortic lesions, establishing its role in vascular disease. In addition, this protein has been shown to have an antimicrobial function, inhibiting the replication of herpes simplex virus. Alternative splicing results in multiple transcript variants encoding a single protein.
Function As an inhibitor of cysteine proteinases, this protein is thought to serve an important physiological role as a local regulator of this enzyme activity.
Cellular Localization Amyloid, Secreted
PTM Disulfide bond, Glycoprotein, Phosphoprotein
Title Download Link
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