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Product Description
Human Striatin-4 (STRN4) ELISA Kit | AE15741HU | Abebio
Species Reactivity: Human (Homo sapiens)
Abbreviation: STRN4
Alternative Name: FLJ35594; ZIN; zinedin; zinedin
Application: ELISA
Range: Request Information
Sensitivity: Request Information
Intra-Assay: ≤4.6%
Inter-Assay: ≤7.4%
Recovery: 0, 85
Sample Type: Serum, Plasma, Other biological fluids
Detection Method: Sandwich
Analysis Method : Quantitive
Test Principale: This assay employs a two-site sandwich ELISA to quantitate STRN4 in samples. An antibody specific for STRN4 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anySTRN4 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for STRN4 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of STRN4 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview: Zinedin, a "novel" protein described here, and SG2NA share with striatin identical protein-protein interaction domains and the same overall domain structure. A phylogenetic analysis supports the hypothesis that they constitute a multigenic family deriving from an ancestral gene. DNA probes and antibodies raised against specific domains of each protein showed that zinedin is mainly expressed in the central nervous system, whereas SG2NA, of more widespread occurrence, is mainly expressed in the brain and muscle. All three proteins are both cytosolic and membrane-bound. All three bind calmodulin in the presence of Ca (2+) . In rat brain, SG2NA and striatin are generally not found in the same neurons. Both localize to the soma and dendrites, suggesting that they share a similar type of addressing and closely related functions.
Stability: The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calculated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C) .
