RAB0232

Human IGFBP-1 ELISA Kit

Name: Human IGFBP-1 ELISA Kit
Brand: SIGMA

for serum, plasma, cell culture supernatant and urine

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About This Item

NACRES:

NA.32

UNSPSC Code:

41116158

Product Name

Human IGFBP-1 ELISA Kit, for serum, plasma, cell culture supernatant and urine

species reactivity

human

packaging

kit of 96 wells (12 strips x 8 wells)

technique(s)

ELISA: suitable
capture ELISA: suitable

input

sample type plasma
sample type serum
sample type cell culture supernatant(s)
sample type urine

assay range

inter-assay cv: <12%
intra-assay cv: <10%
sensitivity: 5 pg/mL
standard curve range: 2.74-2000 pg/mL

detection method

colorimetric

shipped in

wet ice

storage temp.

−20°C

Gene Information

human ... IGFBP1(3484)

Related Categories

Enzyme-Linked Immunosorbent Assay (ELISA) Kits

Immunoassay Platform Solutions

Application

For research use only. Not for use in diagnostic procedures.
Please refer to the attached General ELISA KIT Procedure (sandwich, competitive & Indirect ELISA)

General description

The Human IGF-BP-1 ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of human IGF-BP-1 in serum, plasma, cell culture supernatants and urine.

Immunogen

Recombinant Human IGFBP1

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.

pictograms

GHS05

signalword

Warning

hcodes

H290

pcodes

P234 - P390

Hazard Classifications

Met. Corr. 1

Storage Class

8A - Combustible corrosive hazardous materials

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Complement and other immune-related factors in cervicovaginal fluid associated with intra-amniotic infection/inflammation and spontaneous preterm delivery in women with preterm labor.

Subeen Hong et al.

Archives of gynecology and obstetrics, 301(6), 1431-1439 (2020-05-06)

To investigate whether complement and other immune-related proteins in cervicovaginal fluid (CVF) can predict intra-amniotic infection and/or inflammation (IAI) and spontaneous preterm delivery (SPTD, < 34.0 weeks) in women with preterm labor (PTL) and to compare the predictive abilities of these biomarkers with

Unique Associations between Insulin-Like Growth Factor Binding Protein-1, Insulin-Like Growth Factor-1 and T Cell Immunoglobulin Mucin 3 in Successful Twin Pregnancies Conceived with Donor Oocytes.

Giovanni Sisti et al.

Medicina (Kaunas, Lithuania), 55(5) (2019-05-19)

Background and Objectives: To investigate if pregnancies conceived using an oocyte donor necessitate an alteration in immune regulation, we compared concentrations of insulin-like growth factor binding protein (IGFBP)-1, insulin-like growth factor (IGF)-1 and T cell immunoglobulin mucin-3 (Tim-3) in women

Starvation reduces hyaluronan synthesis by suppressing TGF-β1/IGF-I signaling in rat skin.

Takumi Yamane et al.

Bioscience, biotechnology, and biochemistry, 83(3), 511-517 (2018-11-13)

Although starvation has been reported to influence the functions of various tissues, its effects on the skin are not well understood. In this study, we investigated the effect of starvation on hyaluronan synthesis in rat skin. Starvation reduced hyaluronan synthesis

Insulin-like growth factor binding protein-1 predicts preterm premature rupture of membranes in twin pregnancies.

Giovanni Sisti et al.

Archives of gynecology and obstetrics, 300(3), 583-587 (2019-06-16)

Mechanisms leading to preterm premature rupture of membranes (PPROM) remain incompletely defined. Based on the elevated occurrence of PPROM in twin gestations and recent studies of the involvement of insulin-like growth factor binding protein-1 (IGFBP-1) in the inhibition of collagen

Icaritin inhibits decidualization of endometrial stromal cells.

Aiwen Le et al.

Experimental and therapeutic medicine, 14(6), 5949-5955 (2017-12-30)

The aim of the present study was to investigate the effects of Icaritin on the proliferation and decidualization of endometrial stromal cells (ESCs). A total of 20 specimens of endometrium were collected during hysterectomy at the Gynecology Department of Shenzhen

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