human placenta large insert cdna library Search Results


99
Thermo Fisher gene exp cdh1 mm01247357 m1
Gene Exp Cdh1 Mm01247357 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+placenta+large+insert+cdna+library/Gene+Exp%2E+Cdh1%2C+Mm01247357_m1/ppr0560555-368-112--1
Average 99 stars, based on 1 article reviews
gene exp cdh1 mm01247357 m1 - by Bioz Stars, 2026-09
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90
GenHunter Corporation thermostable human placental alkaline phosphatase (ap
Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of <t>human</t> SPARC and a <t>thermostable</t> human <t>placental</t> <t>alkaline</t> <t>phosphatase</t> (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.
Thermostable Human Placental Alkaline Phosphatase (Ap, supplied by GenHunter Corporation, 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/human+placenta+large+insert+cdna+library/alkaline+phosphatase++ap++fusion+protein/pmc01850537-120-24-35
Average 90 stars, based on 1 article reviews
thermostable human placental alkaline phosphatase (ap - by Bioz Stars, 2026-09
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90
R&D Systems goat anti human e cadherin primary antibody
Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of <t>human</t> SPARC and a <t>thermostable</t> human <t>placental</t> <t>alkaline</t> <t>phosphatase</t> (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.
Goat Anti Human E Cadherin Primary Antibody, supplied by R&D Systems, 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/human+placenta+large+insert+cdna+library/Human+Cadherin-11+PE-conjugated+Antibody/pmc03611242-128-4-9
Average 90 stars, based on 1 article reviews
goat anti human e cadherin primary antibody - by Bioz Stars, 2026-09
90/100 stars
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90
Corning Life Sciences human placental collagen–coated 6.5-mm transwell inserts
Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of <t>human</t> SPARC and a <t>thermostable</t> human <t>placental</t> <t>alkaline</t> <t>phosphatase</t> (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.
Human Placental Collagen–Coated 6.5 Mm Transwell Inserts, supplied by Corning Life Sciences, 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/human+placenta+large+insert+cdna+library/human+placental+collagen+coated+6+5+mm+transwell+inserts/pmc07055692-83-12-14
Average 90 stars, based on 1 article reviews
human placental collagen–coated 6.5-mm transwell inserts - by Bioz Stars, 2026-09
90/100 stars
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90
Corning Life Sciences porous support 24-well transwell inserts
Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of <t>human</t> SPARC and a <t>thermostable</t> human <t>placental</t> <t>alkaline</t> <t>phosphatase</t> (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.
Porous Support 24 Well Transwell Inserts, supplied by Corning Life Sciences, 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/human+placenta+large+insert+cdna+library/96+well+plates/pm33542495-104-20-31
Average 90 stars, based on 1 article reviews
porous support 24-well transwell inserts - by Bioz Stars, 2026-09
90/100 stars
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94
R&D Systems dr9046658 af1075 sp r d systems e cadherin mouse
Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of <t>human</t> SPARC and a <t>thermostable</t> human <t>placental</t> <t>alkaline</t> <t>phosphatase</t> (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.
Dr9046658 Af1075 Sp R D Systems E Cadherin Mouse, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+placenta+large+insert+cdna+library/Human+Cerberus+1+Antibody/pm37369348-1021-67-69
Average 94 stars, based on 1 article reviews
dr9046658 af1075 sp r d systems e cadherin mouse - by Bioz Stars, 2026-09
94/100 stars
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90
Imedex LLC human placental collagen type iv/ivox
Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of <t>human</t> SPARC and a <t>thermostable</t> human <t>placental</t> <t>alkaline</t> <t>phosphatase</t> (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.
Human Placental Collagen Type Iv/Ivox, supplied by Imedex LLC, 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/human+placenta+large+insert+cdna+library/human+collagens/pm16202409-66-11-24
Average 90 stars, based on 1 article reviews
human placental collagen type iv/ivox - by Bioz Stars, 2026-09
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Placenta Growth Factor-1 Human Recombinant produced in insect cells is a homodimer, glycosylated polypeptide chain containing 2 x 131 amino acids and having a total molecular mass of approximately 34 kDa. The PLGF-1 is purified
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Recombinant Human Placenta Growth Factor-1 (PlGF-1) is a 19 kDa protein produced ininsect cellsas a homodimer containing 131 amino acid residues andwith a C-terminal His-tag (6x His).Human Placenta Growth Factor (PlGF) is a polypeptide growth
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Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of human SPARC and a thermostable human placental alkaline phosphatase (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.

Journal:

Article Title: SPARC (Secreted Protein Acidic and Rich in Cysteine) Induces Apoptosis in Ovarian Cancer Cells

doi:

Figure Lengend Snippet: Cell surface receptor binding assays of HOSE cells and ovarian cancer cells. A secreted SPARC-AP fusion protein consists of human SPARC and a thermostable human placental alkaline phosphatase (AP) was used to examine the presence of putative SPARC receptors in ovarian cells. As background control, a secretory AP protein produced by the 293T/pAPtag-4 stable cell line was also used in this assay. Cells incubated with culture medium containing SPARC-AP or AP proteins were washed, lysed, and assayed for AP activities. Increase in ligand binding is indicated by the increase in AP activity, which is quantified by measuring absorbance at 405 nm. HOSE1-15 cells showed high levels of binding, whereas the three ovarian cancer cell lines studied have less binding to the SPARC-AP fusion protein.

Article Snippet: The amplified DNA fragment was digested with Hind III and Bgl II, which was subsequently inserted in-frame upstream of the coding sequence of a thermostable human placental alkaline phosphatase (AP) in the expression vector pAPtag-2 (GenHunter Corp., Nashville, TN).

Techniques: Cell Surface Receptor Assay, Binding Assay, Produced, Stable Transfection, Incubation, Ligand Binding Assay, Activity Assay