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rhigf-2  (Diagnostic Products Corp)

 
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    Diagnostic Products Corp rhigf-2
    Rhigf 2, supplied by Diagnostic Products Corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rhigf-2/rhigf+2/pm20106611-49-11-14
    Average 90 stars, based on 1 article reviews
    rhigf-2 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Binding Assay:

    Article Title: Placental gene expression is related to glucose metabolism and fetal cord blood levels of insulin and insulin-like growth factors in intrauterine growth restriction.
    Article Snippet: Contents lists available at ScienceDirect Early Human Development j ourna l homepage: www.e lsev ie r.com/ locate /ear lhumdev Placental gene expression is related to glucose metabolism and fetal cord blood levels of insulin and insulin-like growth factors in intrauterine growth restriction Mi Hee Lee a, Yeo Jin Jeon a, Sang Mi Lee b, Mi Hye Park c, Sung-Chul Jung a, Young Ju Kim c,⁎ a Department of Biochemistry, School of Medicine, Ewha Womans University, Seoul, Republic of Korea b Department of Molecular Medicine, School of Medicine, Ewha Womans University, Seoul, Republic of Korea c Department of Obstetrics and Gynecology, School of Medicine, Ewha Womans University, Seoul, Republic of Korea ⁎ Corresponding author.. Department of Obstetrics an University MokDong Hospital, Seoul 158-051, Republi 5029; fax: +82 2 2647 9860.. E-mail address: kkyj@ewha.ac.kr (Y.J.

    Incubation:

    Article Title: Placental gene expression is related to glucose metabolism and fetal cord blood levels of insulin and insulin-like growth factors in intrauterine growth restriction.
    Article Snippet: Contents lists available at ScienceDirect Early Human Development j ourna l homepage: www.e lsev ie r.com/ locate /ear lhumdev Placental gene expression is related to glucose metabolism and fetal cord blood levels of insulin and insulin-like growth factors in intrauterine growth restriction Mi Hee Lee a, Yeo Jin Jeon a, Sang Mi Lee b, Mi Hye Park c, Sung-Chul Jung a, Young Ju Kim c,⁎ a Department of Biochemistry, School of Medicine, Ewha Womans University, Seoul, Republic of Korea b Department of Molecular Medicine, School of Medicine, Ewha Womans University, Seoul, Republic of Korea c Department of Obstetrics and Gynecology, School of Medicine, Ewha Womans University, Seoul, Republic of Korea ⁎ Corresponding author.. Department of Obstetrics an University MokDong Hospital, Seoul 158-051, Republi 5029; fax: +82 2 2647 9860.. E-mail address: kkyj@ewha.ac.kr (Y.J.

    Inter Assay:

    Article Title: Placental gene expression is related to glucose metabolism and fetal cord blood levels of insulin and insulin-like growth factors in intrauterine growth restriction.
    Article Snippet: Contents lists available at ScienceDirect Early Human Development j ourna l homepage: www.e lsev ie r.com/ locate /ear lhumdev Placental gene expression is related to glucose metabolism and fetal cord blood levels of insulin and insulin-like growth factors in intrauterine growth restriction Mi Hee Lee a, Yeo Jin Jeon a, Sang Mi Lee b, Mi Hye Park c, Sung-Chul Jung a, Young Ju Kim c,⁎ a Department of Biochemistry, School of Medicine, Ewha Womans University, Seoul, Republic of Korea b Department of Molecular Medicine, School of Medicine, Ewha Womans University, Seoul, Republic of Korea c Department of Obstetrics and Gynecology, School of Medicine, Ewha Womans University, Seoul, Republic of Korea ⁎ Corresponding author.. Department of Obstetrics an University MokDong Hospital, Seoul 158-051, Republi 5029; fax: +82 2 2647 9860.. E-mail address: kkyj@ewha.ac.kr (Y.J.



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    SPR direct binding and competition assays show similar ligand binding affinities for IGF-TRAP 3.1 and IGF-TRAP 3.3. Direct ligand binding was measured by first capturing the IGF-TRAP onto an immobilize anti-Fc surface (4000 resonance units (RUs)), and then flowing a dilution series of the ligands indicated over the captured IGF-TRAP. Shown in (A-top) are results of binding sensorgrams of a representative analysis of a total of 3 performed. The kinetic fits used for affinity determination are shown in green. The calculated affinity constants (mean ± SD, n = 3) based on a fit to a 1:1 Langmuir binding model are shown in the Table ( A -bottom). Shown in ( B ) are results of a binding competition assay in which increasing concentrations of IGF-TRAP-3.1 or IGF-TRAP-3.3 were used to compete with binding of constant ligand concentrations to MAb MEDI-573-immobilized onto the SPR surface. The SPR response of IGF binding to MEDI-573 is shown (B-top) with IGF-TRAP-3.1 (in red), IGF-TRAP-3.3 (in green) and using rhIGF-1 (circles) or <t>rhIGF-2</t> (triangles) as ligands. Shown in (B-bottom) are IC50 values for IGF-TRAP-3.1 and IGF-TRAP-3.3 with the 95% CI (in parentheses) as determined based on the SPR competition binding assays.
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    Image Search Results


    SPR direct binding and competition assays show similar ligand binding affinities for IGF-TRAP 3.1 and IGF-TRAP 3.3. Direct ligand binding was measured by first capturing the IGF-TRAP onto an immobilize anti-Fc surface (4000 resonance units (RUs)), and then flowing a dilution series of the ligands indicated over the captured IGF-TRAP. Shown in (A-top) are results of binding sensorgrams of a representative analysis of a total of 3 performed. The kinetic fits used for affinity determination are shown in green. The calculated affinity constants (mean ± SD, n = 3) based on a fit to a 1:1 Langmuir binding model are shown in the Table ( A -bottom). Shown in ( B ) are results of a binding competition assay in which increasing concentrations of IGF-TRAP-3.1 or IGF-TRAP-3.3 were used to compete with binding of constant ligand concentrations to MAb MEDI-573-immobilized onto the SPR surface. The SPR response of IGF binding to MEDI-573 is shown (B-top) with IGF-TRAP-3.1 (in red), IGF-TRAP-3.3 (in green) and using rhIGF-1 (circles) or rhIGF-2 (triangles) as ligands. Shown in (B-bottom) are IC50 values for IGF-TRAP-3.1 and IGF-TRAP-3.3 with the 95% CI (in parentheses) as determined based on the SPR competition binding assays.

    Journal: Scientific Reports

    Article Title: Enhanced anti-metastatic bioactivity of an IGF-TRAP re-engineered to improve physicochemical properties

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    Figure Lengend Snippet: SPR direct binding and competition assays show similar ligand binding affinities for IGF-TRAP 3.1 and IGF-TRAP 3.3. Direct ligand binding was measured by first capturing the IGF-TRAP onto an immobilize anti-Fc surface (4000 resonance units (RUs)), and then flowing a dilution series of the ligands indicated over the captured IGF-TRAP. Shown in (A-top) are results of binding sensorgrams of a representative analysis of a total of 3 performed. The kinetic fits used for affinity determination are shown in green. The calculated affinity constants (mean ± SD, n = 3) based on a fit to a 1:1 Langmuir binding model are shown in the Table ( A -bottom). Shown in ( B ) are results of a binding competition assay in which increasing concentrations of IGF-TRAP-3.1 or IGF-TRAP-3.3 were used to compete with binding of constant ligand concentrations to MAb MEDI-573-immobilized onto the SPR surface. The SPR response of IGF binding to MEDI-573 is shown (B-top) with IGF-TRAP-3.1 (in red), IGF-TRAP-3.3 (in green) and using rhIGF-1 (circles) or rhIGF-2 (triangles) as ligands. Shown in (B-bottom) are IC50 values for IGF-TRAP-3.1 and IGF-TRAP-3.3 with the 95% CI (in parentheses) as determined based on the SPR competition binding assays.

    Article Snippet: Recombinant human (rh) IGF-1 for KIRA assay was obtained from the National Institute of Biological Standards and Calibrators (NIBSC, Hertfordshire, UK) (02/254). rhIGF-1 and rhIGF-2 and insulin used for surface plasmon resonance (SPR) experiments were from Sigma-Aldrich (Oakville, ON, Canada) and recombinant mouse IGF-1 was from Cedarlane (Burlington, ON, Canada).

    Techniques: Binding Assay, Ligand Binding Assay, Competitive Binding Assay