Human FABP5/E-FABP ELISA Kit (DEIABL528)

Regulatory status: For research use only, not for use in diagnostic procedures.

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Size
96T
Sample
serum, plasma, saliva
Species Reactivity
Human
Intended Use
This Human FABP5/E-FABP ELISA Kit is used for the quantitative measurement of human FABP5/E-FABP in serum, plasma, and saliva.
Individual users should determine appropriate conditions when using other types of samples.
This assay kit is for research use only and not for use in diagnostic or therapeutic procedures.
Storage
- Upon receipt store all components at 4°C.
- Don't expose reagents to excessive light.
Precision
Intra-assay (Within-Run, n=16) CV=2.9, 1.8, 4.7 %
Inter-assay (Run-to-Run, n=5) CV=10.2, 5.7, 6.2 %
Sensitivity
The limit of detection (defined as such a concentration of human FABP5/E-FABP giving absorbance higher than mean absorbance of blank* plus three standard deviations of the absorbance of blank: A blank + 3SD blank) is better than 228 pg/mL of sample.
General Description
Fatty acid-binding proteins (FABPs) are a class of cytoplasmic proteins that bind long chain fatty acids. FABPs are small intracellular proteins (~13-14 kDa) with a high degree of tissue specificity. They are abundantly present in various cell types and play an important role in the intracellular utilization of fatty acids, transport and metabolism. There are at least nine distinct types of FABP, each showing a specific pattern of tissue expression.
Epidermal fatty acid binding protein (E-FABP and FABP5, and also called mal1 in mice) belongs to the intracellular FABP family and is expressed in differentiated adipocytes, macrophages, skin, brain, mammary glands and so on. Human FABP5/E-FABP has a high degree of homology to aP2 (mouse FABP4) and is also an important player in obesity-related disorders. FABP5/E-FABP/mal1 knockout mice exhibited enhanced insulin-stimulated glucose uptake and increased systemic insulin sensitivity, while transgenic overexpression of FABP5/E-FABP aggravated insulin resistance and hyperglycemia. Conversely, a marked compensatory up-regulation of adipocyte FABP5/E-FABP expression was observed in FABP4/ aP2-deficient mice.

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