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Key Documents

SRP3062

Sigma-Aldrich

IGF-Binding Protein 1 human

recombinant, expressed in E. coli, ≥98% (SDS-PAGE), ≥98% (HPLC), suitable for cell culture

Sinónimos:

IBP-1, Placenta Protein 12 (PP12)

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About This Item

Código UNSPSC:
51111800
NACRES:
NA.32

origen biológico

human

recombinante

expressed in E. coli

Análisis

≥98% (HPLC)
≥98% (SDS-PAGE)

formulario

lyophilized

potencia

<0.5 μg/mL

mol peso

25.4 kDa

envase

pkg of 25 μg

técnicas

cell culture | mammalian: suitable

impurezas

<0.1 EU/μg endotoxin, tested

color

white to off-white

Nº de acceso UniProt

Condiciones de envío

wet ice

temp. de almacenamiento

−20°C

Información sobre el gen

human ... IGFBP1(3484)

Descripción general

Insulin-like growth factor-binding proteins (IGF-BPs) form high affinity complexes with both insulin-like growth factor- I and II (IGF-I and IGF-II). Currently there are seven named IGF-BPs. Insulin-like growth factor-binding protein-1 (IGF-BP1) is a 25.4kDa cysteine-rich secreted protein. It is the most abundant IGF-BP in amniotic fluid and is expressed in liver, decidua and kidneys. Levels of IGF-BP1 in serum are lowest after food. It binds to both IGF-I and IGF-II with equal affinity. Phosphorylated IGF-BP1 hinders IGF actions, whereas non-phosphorylated IGF-BP1 is stimulatory. Recombinant human IGF-BP1 is a 25.4kDa protein consisting of 235 amino acid residues (Isoform A).

Acciones bioquímicas o fisiológicas

Insulin-like growth factor-binding proteins (IGF-BPs) control the distribution, function and activity of insulin-like growth factors (IGFs) in various cell tissues and body fluids. They prolong the half-life of IGFs. Insulin-like growth factor-binding protein-1 (IGF-BP1) has been shown to have a role in the development and advancement of cancers. It is downregulated in hepatocellular carcinoma.

Secuencia

MAPWQCAPCS AEKLALCPPV SASCSEVTRS AGCGCCPMCA LPLGAACGVA TARCARGLSC RALPGEQQPL HALTRGQGAC VQESDASAPH AAEAGSPESP ESTEITEEEL LDNFHLMAPS EEDHSILWDA ISTYDGSKAL HVTNIKKWKE PCRIELYRVV ESLAKAQETS GEEISKFYLP NCNKNGFYHS RQCETSMDGE AGLCWCVYPW NGKRIPGSPE IRGDPNCQIY FNVQN

Forma física

Lyophilized from 10 mM Sodium Phosphate, pH 7.5.

Reconstitución

Centrifuge the vial prior to opening. Reconstitute in water to a concentration of 0.1-1.0 mg/ml. Do not vortex. This solution can be stored at 2-8°C for up to 1 week. For extended storage, it is recommended to further dilute in a buffer containing a carrier protein (example 0.1% BSA) and store in working aliquots at -20°C to -80°C.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Hiroyasu Kamei et al.
PloS one, 3(8), e3091-e3091 (2008-09-05)
Gene duplication is the primary force of new gene evolution. Deciphering whether a pair of duplicated genes has evolved divergent functions is often challenging. The zebrafish is uniquely positioned to provide insight into the process of functional gene evolution due
Over-expression of insulin-like growth factor binding protein-related protein-1(IGFBP-rP1/mac25) in the M12 prostate cancer cell line alters tumor growth by a delay in G1 and cyclin A associated apoptosis.
Ezzat V.A., et al.
Diabetes, obesity & metabolism, 3, 198-211 (2008)
Carnosine decreases IGFBP1 production in db/db mice through suppression of HIF-1.
Forsberg EA
The Journal of Endocrinology, 225(3), 159-167 (2015)
The extracellular regulation of growth factor action.
Flaumenhaft R
Molecular Biology of the Cell, 3(10), 1057-1065 (1992)
C Mannelli et al.
Mediators of inflammation, 2014, 635364-635364 (2014-04-17)
A proper fetomaternal immune-endocrine cross-talk in pregnancy is fundamental for reproductive success. This might be unbalanced by exposure to environmental chemicals, such as bisphenol A (BPA). As fetoplacental contamination with BPA originates from the maternal compartment, this study investigated the

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