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About This Item
NACRES:
NA.32
UNSPSC Code:
41116158
Product Name
Mouse IGF-I ELISA Kit, for serum, plasma and cell culture supernatant
species reactivity
mouse
packaging
kit of 96 wells (12 strips x 8 wells)
technique(s)
ELISA: suitable
capture ELISA: suitable
input
sample type cell culture supernatant(s)
sample type serum
sample type plasma
assay range
inter-assay cv: <12%
intra-assay cv: <10%
sensitivity: 4 pg/mL
standard curve range: 2.74-2000 pg/mL
detection method
colorimetric
shipped in
wet ice
storage temp.
−20°C
Gene Information
mouse ... Igf1(16000)
Related Categories
Application
For research use only. Not for use in diagnostic procedures.
Mouse IGF-I ELISA kit has been used to measure plasma IGF-I (Insulin-like growth factor-I) level from Igf1r L/L and BAT-specific Igf1r-knockout (BATIGFIRKO) mice.
Mouse IGF-I ELISA kit has been used to measure plasma IGF-I (Insulin-like growth factor-I) level from Igf1r L/L and BAT-specific Igf1r-knockout (BATIGFIRKO) mice.
For research use only. Not for use in diagnostic procedures.
Please refer to the attached General ELISA KIT Procedure (sandwich, competitive & Indirect ELISA)
Please refer to the attached General ELISA KIT Procedure (sandwich, competitive & Indirect ELISA)
Mouse IGF-I ELISA Kit has been used to measure the concentration of insulin-like growth factor(IGF) secreted by mesenchymal stem cells(MSCs). It has also been used to measure the level of IGF1 in blood samples of mice.
Biochem/physiol Actions
IGF-I (Insulin-like growth factor-I) is required for fetal growth and development. It is also involved in the growth and repair of heart tissues. IGF-I has been linked to neuroplasticity and hippocampal neurogenesis. It is important in the recovery from ischaemic injury. IGF-I also facilitates the differentiation of adipocytes and other cells.
General description
The Mouse IGF-I ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of mouse IGF-I in serum, plasma, cell culture supernatants and urine.
Immunogen
Recombinant Mouse IGF-I
Other Notes
A sample Certificate of Analysis is available for this product.
Please type the word sample in the text box provided for lot number.
Please type the word sample in the text box provided for lot number.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Met. Corr. 1
Storage Class
8A - Combustible corrosive hazardous materials
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Flavia R Siqueira et al.
Physiology & behavior, 154, 68-75 (2015-11-26)
A low-salt (LS) diet during pregnancy has been linked to insulin resistance in adult offspring, at least in the experimental setting. However, it remains unclear if this effect is due to salt restriction during early or late pregnancy. To better
B A Taylor et al.
Cytogenetics and cell genetics, 56(1), 57-58 (1991-01-01)
The peptide hormone, insulin-like growth factor I (IGF-I), is a major determinant of growth in mammals, and also plays a role in differentiation of adipocytes and other cells (Van Wyk, 1984). Although IGF-I is synthesized in many cell types, the
María Llorens-Martín et al.
The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry, 15(2), 134-148 (2009-03-25)
This review addresses the role of serum insulin-like growth factor 1 (IGF1) as one mechanism of adult neural plasticity, specifically, its regulation of hippocampal neurogenesis among other plasticity-related processes. It is suggested that IGF has been reused advantageously both for
He He et al.
Inflammation, 38(6), 2178-2184 (2015-06-25)
Sepsis-induced myocardial injury (SIMI) is caused by various mechanisms. The aim of this study was to investigate the effects of salidroside (Sal) on SIMI and its mechanisms in rats. The sepsis model was established by intraperitoneal injection of lipopolysaccharide (LPS)
Junjie Gao et al.
Science advances, 5(11), eaaw7215-eaaw7215 (2019-12-05)
Mitochondrial transfer plays a crucial role in the regulation of tissue homeostasis and resistance to cancer chemotherapy. Osteocytes have interconnecting dendritic networks and are a model to investigate its mechanism. We have demonstrated, in primary murine osteocytes with photoactivatable mitochondria
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