insulin growth factor 2 igf2 protein Search Results


sirna  (MedChemExpress)
95
MedChemExpress sirna
Sirna, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/insulin+growth+factor+2+igf2+protein/IGF2BP3%2C+Human/pm39837470-121-12-25
Average 95 stars, based on 1 article reviews
sirna - by Bioz Stars, 2026-10
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anti zbp1  (Boster Bio)
93
Boster Bio anti zbp1
Anti Zbp1, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/insulin+growth+factor+2+igf2+protein/Anti-IGF2BP1+Antibody/pmc13006297-220-20-27
Average 93 stars, based on 1 article reviews
anti zbp1 - by Bioz Stars, 2026-10
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anti igf2bp2 anti mettl16 anti m 6 a  (MedChemExpress)
95
MedChemExpress anti igf2bp2 anti mettl16 anti m 6 a
FTH1 acted as the target of <t>METTL16.</t> A The immunofluorescence assay showed the subcellular localization of METTL16 and FTH1. B The binding motif sites of METTL16 for its target genes (GGAAC). C The FTH1 level in cervical cancer cells was test by the RT-PCR. D RNA immunoprecipitation (RIP) assay was conducted for the binding within METTL16 and FTH1 in HeLa cells. E RIP assay using anti-m 6 A conducted for the m 6 A modification on FTH1 mRNA. * p < 0.05, ** p < 0.01
Anti Igf2bp2 Anti Mettl16 Anti M 6 A, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/insulin+growth+factor+2+igf2+protein/IGF2BP2%2C+Human/pmc12905035-39-19-11
Average 95 stars, based on 1 article reviews
anti igf2bp2 anti mettl16 anti m 6 a - by Bioz Stars, 2026-10
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whole imp 3 protein  (ProSci Incorporated)
90
ProSci Incorporated whole imp 3 protein
FTH1 acted as the target of <t>METTL16.</t> A The immunofluorescence assay showed the subcellular localization of METTL16 and FTH1. B The binding motif sites of METTL16 for its target genes (GGAAC). C The FTH1 level in cervical cancer cells was test by the RT-PCR. D RNA immunoprecipitation (RIP) assay was conducted for the binding within METTL16 and FTH1 in HeLa cells. E RIP assay using anti-m 6 A conducted for the m 6 A modification on FTH1 mRNA. * p < 0.05, ** p < 0.01
Whole Imp 3 Protein, supplied by ProSci Incorporated, 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/insulin+growth+factor+2+igf2+protein/IMP-3+Recombinant+Protein/us09770498-767-16-22
Average 90 stars, based on 1 article reviews
whole imp 3 protein - by Bioz Stars, 2026-10
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myc igf2bp2  (Shanghai Korain Biotech Co Ltd)
93
Shanghai Korain Biotech Co Ltd myc igf2bp2
FTH1 acted as the target of <t>METTL16.</t> A The immunofluorescence assay showed the subcellular localization of METTL16 and FTH1. B The binding motif sites of METTL16 for its target genes (GGAAC). C The FTH1 level in cervical cancer cells was test by the RT-PCR. D RNA immunoprecipitation (RIP) assay was conducted for the binding within METTL16 and FTH1 in HeLa cells. E RIP assay using anti-m 6 A conducted for the m 6 A modification on FTH1 mRNA. * p < 0.05, ** p < 0.01
Myc Igf2bp2, supplied by Shanghai Korain Biotech Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/insulin+growth+factor+2+igf2+protein/Human+Insulin-like+Growth+Factor+2+MRNA-binding+Protein+2/pm38281999-108-0-13
Average 93 stars, based on 1 article reviews
myc igf2bp2 - by Bioz Stars, 2026-10
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r es ama1  (Boster Bio)
94
Boster Bio r es ama1
Trial design and vaccine procedures
R Es Ama1, supplied by Boster Bio, 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/insulin+growth+factor+2+igf2+protein/Anti-IGF2BP1+Antibody/pmc09623944-83-2-15
Average 94 stars, based on 1 article reviews
r es ama1 - by Bioz Stars, 2026-10
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igf ii protein  (Kingfisher Biotech)
94
Kingfisher Biotech igf ii protein
Trial design and vaccine procedures
Igf Ii Protein, supplied by Kingfisher Biotech, 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/insulin+growth+factor+2+igf2+protein/Bovine+IGF-2+Recombinant+Protein/pm31293026-58-17-20
Average 94 stars, based on 1 article reviews
igf ii protein - by Bioz Stars, 2026-10
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mrna-binding proteins regulating insulin-like growth factor 2 (igf2) translation  (Informa UK Limited)
90
Informa UK Limited mrna-binding proteins regulating insulin-like growth factor 2 (igf2) translation
Trial design and vaccine procedures
Mrna Binding Proteins Regulating Insulin Like Growth Factor 2 (Igf2) Translation, supplied by Informa UK Limited, 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/insulin+growth+factor+2+igf2+protein/mrna+binding+proteins+regulating+insulin+like+growth+factor+2++igf2++translation/pm30371117-29-19-5
Average 90 stars, based on 1 article reviews
mrna-binding proteins regulating insulin-like growth factor 2 (igf2) translation - by Bioz Stars, 2026-10
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Image Search Results


FTH1 acted as the target of METTL16. A The immunofluorescence assay showed the subcellular localization of METTL16 and FTH1. B The binding motif sites of METTL16 for its target genes (GGAAC). C The FTH1 level in cervical cancer cells was test by the RT-PCR. D RNA immunoprecipitation (RIP) assay was conducted for the binding within METTL16 and FTH1 in HeLa cells. E RIP assay using anti-m 6 A conducted for the m 6 A modification on FTH1 mRNA. * p < 0.05, ** p < 0.01

Journal: Discover Oncology

Article Title: Novel N 6 -methyladenosine (m 6 A) writer METTL16 promotes the cervical cancer tumorigenesis by targeting FTH1-dependent ferroptosis

doi: 10.1007/s12672-026-04403-8

Figure Lengend Snippet: FTH1 acted as the target of METTL16. A The immunofluorescence assay showed the subcellular localization of METTL16 and FTH1. B The binding motif sites of METTL16 for its target genes (GGAAC). C The FTH1 level in cervical cancer cells was test by the RT-PCR. D RNA immunoprecipitation (RIP) assay was conducted for the binding within METTL16 and FTH1 in HeLa cells. E RIP assay using anti-m 6 A conducted for the m 6 A modification on FTH1 mRNA. * p < 0.05, ** p < 0.01

Article Snippet: Cervical cancer cells were lysed by immunoprecipitation buffer (protease, phosphatase inhibitors, MCE) containing magnetic beads conjugated to specific antibodies (anti-IGF2BP2, anti-METTL16, anti-m 6 A).

Techniques: Immunofluorescence, Binding Assay, Reverse Transcription Polymerase Chain Reaction, RNA Immunoprecipitation, Modification

IGF2BP2 promoted the stability of FTH1 mRNA. A The immunofluorescent staining showed the subcellular localization of IGF2BP2 and FTH1 in HeLa cells. B The positive correlation within IGF2BP2 and FTH1 in clinical samples ( http://gepia.cancer-pku.cn/index.html ). C RNA immunoprecipitation (RIP) assay showed the immunoprecipitated FTH1 mRNA by anti-IGF2BP2 antibody. D RNA decay analysis reported the stability of FTH1 mRNA in cervical cancer cells with IGF2BP2 overexpression. E RNA decay analysis reported the stability of FTH1 mRNA in cervical cancer cells with METTL16 silencing (sh-METTL16-1, sh-METTL16-2). F RNA decay analysis reported the stability of FTH1 mRNA in cervical cancer cells with IGF2BP2 silencing (si-IGF2BP2) and METTL16 overexpression. * p < 0.05, ** p < 0.01

Journal: Discover Oncology

Article Title: Novel N 6 -methyladenosine (m 6 A) writer METTL16 promotes the cervical cancer tumorigenesis by targeting FTH1-dependent ferroptosis

doi: 10.1007/s12672-026-04403-8

Figure Lengend Snippet: IGF2BP2 promoted the stability of FTH1 mRNA. A The immunofluorescent staining showed the subcellular localization of IGF2BP2 and FTH1 in HeLa cells. B The positive correlation within IGF2BP2 and FTH1 in clinical samples ( http://gepia.cancer-pku.cn/index.html ). C RNA immunoprecipitation (RIP) assay showed the immunoprecipitated FTH1 mRNA by anti-IGF2BP2 antibody. D RNA decay analysis reported the stability of FTH1 mRNA in cervical cancer cells with IGF2BP2 overexpression. E RNA decay analysis reported the stability of FTH1 mRNA in cervical cancer cells with METTL16 silencing (sh-METTL16-1, sh-METTL16-2). F RNA decay analysis reported the stability of FTH1 mRNA in cervical cancer cells with IGF2BP2 silencing (si-IGF2BP2) and METTL16 overexpression. * p < 0.05, ** p < 0.01

Article Snippet: Cervical cancer cells were lysed by immunoprecipitation buffer (protease, phosphatase inhibitors, MCE) containing magnetic beads conjugated to specific antibodies (anti-IGF2BP2, anti-METTL16, anti-m 6 A).

Techniques: Staining, RNA Immunoprecipitation, Immunoprecipitation, Over Expression

Trial design and vaccine procedures

Journal: Parasites & Vectors

Article Title: Preliminary evaluation of the protective effects of recombinant AMA1 and IMP1 against Eimeria stiedae infection in rabbits

doi: 10.1186/s13071-022-05492-4

Figure Lengend Snippet: Trial design and vaccine procedures

Article Snippet: The separated r Es AMA1 and r Es IMP1 were transferred onto nitrocellulose (NC) membranes (Boster, Wuhan, China), separately.

Techniques: Infection, Sterility, Injection

Multiple sequence alignments of IMP1 and AMA1 from different species. a Multiple alignment of E. stiedae IMP1 with IMP1 proteins from other parasites: Eimeria maxima (UniProt: F4MKA6), Eimeria acervulina (UniProt: U6GHD9), Eimeria tenella (UniProt: F4MKA7), Eimeria mitis (UniProt: U6JVY4), Eimeria praecox (UniProt: U6GBP2); ( b ) multiple alignment of E. stiedae AMA1 with AMA1 proteins from other parasites: Eimeria tenella (UniProt: U6KTA0), Eimeria brunetti (UniProt: U6LBB9), Toxoplasma gondii (UniProt: B6KAM0), Besnoitia besnoiti (UniProt: A0A2A9MBX4), Neospora caninum (UniProt: F0VH85); Blue shading indicates conserved residues. Dashed red boxes represent B-cell epitopes. The transmembrane region is marked with a solid red box

Journal: Parasites & Vectors

Article Title: Preliminary evaluation of the protective effects of recombinant AMA1 and IMP1 against Eimeria stiedae infection in rabbits

doi: 10.1186/s13071-022-05492-4

Figure Lengend Snippet: Multiple sequence alignments of IMP1 and AMA1 from different species. a Multiple alignment of E. stiedae IMP1 with IMP1 proteins from other parasites: Eimeria maxima (UniProt: F4MKA6), Eimeria acervulina (UniProt: U6GHD9), Eimeria tenella (UniProt: F4MKA7), Eimeria mitis (UniProt: U6JVY4), Eimeria praecox (UniProt: U6GBP2); ( b ) multiple alignment of E. stiedae AMA1 with AMA1 proteins from other parasites: Eimeria tenella (UniProt: U6KTA0), Eimeria brunetti (UniProt: U6LBB9), Toxoplasma gondii (UniProt: B6KAM0), Besnoitia besnoiti (UniProt: A0A2A9MBX4), Neospora caninum (UniProt: F0VH85); Blue shading indicates conserved residues. Dashed red boxes represent B-cell epitopes. The transmembrane region is marked with a solid red box

Article Snippet: The separated r Es AMA1 and r Es IMP1 were transferred onto nitrocellulose (NC) membranes (Boster, Wuhan, China), separately.

Techniques: Sequencing

SDS-PAGE and Western blotting analysis of r Es IMP1 ( a ) and r Es AMA1 ( b ). Lane M: Protein molecular weight markers; lanes 1–4: recombinant proteins that were dissolved in the supernatant, 4 M urea, 6 M urea, and 8 M urea after ultrasonication; lane 5: purified recombinant proteins; lane 6: purified recombinant proteins incubated with anti- E. stiedae positive sera; lane 7: purified recombinant proteins incubated with negative sera from coccidia-free rabbits (the bands are indicated using arrows)

Journal: Parasites & Vectors

Article Title: Preliminary evaluation of the protective effects of recombinant AMA1 and IMP1 against Eimeria stiedae infection in rabbits

doi: 10.1186/s13071-022-05492-4

Figure Lengend Snippet: SDS-PAGE and Western blotting analysis of r Es IMP1 ( a ) and r Es AMA1 ( b ). Lane M: Protein molecular weight markers; lanes 1–4: recombinant proteins that were dissolved in the supernatant, 4 M urea, 6 M urea, and 8 M urea after ultrasonication; lane 5: purified recombinant proteins; lane 6: purified recombinant proteins incubated with anti- E. stiedae positive sera; lane 7: purified recombinant proteins incubated with negative sera from coccidia-free rabbits (the bands are indicated using arrows)

Article Snippet: The separated r Es AMA1 and r Es IMP1 were transferred onto nitrocellulose (NC) membranes (Boster, Wuhan, China), separately.

Techniques: SDS Page, Western Blot, Molecular Weight, Recombinant, Purification, Incubation

Protective effects of r Es AMA1 and r Es IMP1 against E. stiedae infection under different evaluation indicators

Journal: Parasites & Vectors

Article Title: Preliminary evaluation of the protective effects of recombinant AMA1 and IMP1 against Eimeria stiedae infection in rabbits

doi: 10.1186/s13071-022-05492-4

Figure Lengend Snippet: Protective effects of r Es AMA1 and r Es IMP1 against E. stiedae infection under different evaluation indicators

Article Snippet: The separated r Es AMA1 and r Es IMP1 were transferred onto nitrocellulose (NC) membranes (Boster, Wuhan, China), separately.

Techniques: Infection

Gross postmortem examinations of the liver. a PBS-uninfected group; ( b ) PBS-infected group; ( c ) Quil-A-infected group; ( d ) Trx-His-S-infected group; ( e ) r Es AMA1 group; ( f ) r Es IMP1 group

Journal: Parasites & Vectors

Article Title: Preliminary evaluation of the protective effects of recombinant AMA1 and IMP1 against Eimeria stiedae infection in rabbits

doi: 10.1186/s13071-022-05492-4

Figure Lengend Snippet: Gross postmortem examinations of the liver. a PBS-uninfected group; ( b ) PBS-infected group; ( c ) Quil-A-infected group; ( d ) Trx-His-S-infected group; ( e ) r Es AMA1 group; ( f ) r Es IMP1 group

Article Snippet: The separated r Es AMA1 and r Es IMP1 were transferred onto nitrocellulose (NC) membranes (Boster, Wuhan, China), separately.

Techniques: Infection

Biochemical estimation of ALT and AST levels in the six groups

Journal: Parasites & Vectors

Article Title: Preliminary evaluation of the protective effects of recombinant AMA1 and IMP1 against Eimeria stiedae infection in rabbits

doi: 10.1186/s13071-022-05492-4

Figure Lengend Snippet: Biochemical estimation of ALT and AST levels in the six groups

Article Snippet: The separated r Es AMA1 and r Es IMP1 were transferred onto nitrocellulose (NC) membranes (Boster, Wuhan, China), separately.

Techniques:

Changes in serum antibody levels. The changes in serum anti-r Es IMP1 ( a ) and r Es AMA1 ( b ) antibody levels after the first vaccination (week 0, indicated by arrows), booster vaccination (week 2, indicated by arrows), and infection with E. stiedae (week 4, indicated by an arrow)

Journal: Parasites & Vectors

Article Title: Preliminary evaluation of the protective effects of recombinant AMA1 and IMP1 against Eimeria stiedae infection in rabbits

doi: 10.1186/s13071-022-05492-4

Figure Lengend Snippet: Changes in serum antibody levels. The changes in serum anti-r Es IMP1 ( a ) and r Es AMA1 ( b ) antibody levels after the first vaccination (week 0, indicated by arrows), booster vaccination (week 2, indicated by arrows), and infection with E. stiedae (week 4, indicated by an arrow)

Article Snippet: The separated r Es AMA1 and r Es IMP1 were transferred onto nitrocellulose (NC) membranes (Boster, Wuhan, China), separately.

Techniques: Infection