anti metap2 Search Results



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Produced in rabbits immunized with purified, recombinant Human MAP2 / METAP2 (rh MAP2 / METAP2; Catalog#10245-H08B; NP_006829.1; Met1-Tyr478). MAP2 / METAP2 specific IgG was purified by Human MAP2 / METAP2 affinity chromatography.
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93
Atlas Antibodies anti metap2 antibody
A . IPA identified the “angiogenesis” annotation to be affected in IUGR twin placentas. B . Immunostaining of CD34 in human placentas from IUGR twins and normal cotwins. CD34 is limited to endothelial cells. Scale bar, 50 μm. C . Placental MVD in IUGR twins and normal cotwins. D . Placental vascular area density in IUGR twins and normal cotwins. E . Immunohistochemical images of EFNB2, VIM, and <t>METAP2</t> in placental shares from IUGR twins and normal cotwins. Scale bar, 100 μm. F – H . EFNB2, VIM, and METAP2 immunostaining intensity per tissue area is represented by the fold-decrease relative to the normal control mean. I – K . qRT-PCR analysis showed that the EFNB2, VIM , and METAP2 transcriptional levels were significantly lower in placentas of IUGR twins compared with normal cotwins. All data are shown as mean ± SD with 6 samples per group. *, P < 0.05; **, P < 0.01; ***, P < 0.001. MVD, microvessel density; NC, negative control; SD, standard deviation.
Anti Metap2 Antibody, supplied by Atlas Antibodies, 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/anti+metap2/Anti-METAP2/med_rxiv__2022__08__29__22278892-180-36-42
Average 93 stars, based on 1 article reviews
anti metap2 antibody - by Bioz Stars, 2026-10
93/100 stars
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Rabbit anti-Human METAP2 Polyclonal Antibody
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Removes the amino-terminal methionine from nascent proteins. The catalytic activity of human METAP2 toward Met-Val peptides is consistently two orders of magnitude higher than that of METAP1, suggesting that it is responsible for processing proteins
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Rabbit anti-Human METAP2 Polyclonal Antibody
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Rabbit Anti METAP2 Polyclonal Affinity Purified (PBS with 0.02% sodium azide, 50% glycerol, pH7.3) (Western Blot) from Innovative Research is a polyclonal antibody in a liquid format, buffered in PBS with 0.02% sodium azide, 50%
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Removes the amino-terminal methionine from nascent proteins. The catalytic activity of human METAP2 toward Met-Val peptides is consistently two orders of magnitude higher than that of METAP1, suggesting that it is responsible for processing proteins
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Rabbit Anti-Human METAP2 (N-term) Antibody, 400 µl
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Image Search Results


A . IPA identified the “angiogenesis” annotation to be affected in IUGR twin placentas. B . Immunostaining of CD34 in human placentas from IUGR twins and normal cotwins. CD34 is limited to endothelial cells. Scale bar, 50 μm. C . Placental MVD in IUGR twins and normal cotwins. D . Placental vascular area density in IUGR twins and normal cotwins. E . Immunohistochemical images of EFNB2, VIM, and METAP2 in placental shares from IUGR twins and normal cotwins. Scale bar, 100 μm. F – H . EFNB2, VIM, and METAP2 immunostaining intensity per tissue area is represented by the fold-decrease relative to the normal control mean. I – K . qRT-PCR analysis showed that the EFNB2, VIM , and METAP2 transcriptional levels were significantly lower in placentas of IUGR twins compared with normal cotwins. All data are shown as mean ± SD with 6 samples per group. *, P < 0.05; **, P < 0.01; ***, P < 0.001. MVD, microvessel density; NC, negative control; SD, standard deviation.

Journal: medRxiv

Article Title: The Proteome Landscape of Human Placentas for Monochorionic Twins with Selective Intrauterine Growth Restriction

doi: 10.1101/2022.08.29.22278892

Figure Lengend Snippet: A . IPA identified the “angiogenesis” annotation to be affected in IUGR twin placentas. B . Immunostaining of CD34 in human placentas from IUGR twins and normal cotwins. CD34 is limited to endothelial cells. Scale bar, 50 μm. C . Placental MVD in IUGR twins and normal cotwins. D . Placental vascular area density in IUGR twins and normal cotwins. E . Immunohistochemical images of EFNB2, VIM, and METAP2 in placental shares from IUGR twins and normal cotwins. Scale bar, 100 μm. F – H . EFNB2, VIM, and METAP2 immunostaining intensity per tissue area is represented by the fold-decrease relative to the normal control mean. I – K . qRT-PCR analysis showed that the EFNB2, VIM , and METAP2 transcriptional levels were significantly lower in placentas of IUGR twins compared with normal cotwins. All data are shown as mean ± SD with 6 samples per group. *, P < 0.05; **, P < 0.01; ***, P < 0.001. MVD, microvessel density; NC, negative control; SD, standard deviation.

Article Snippet: After deparaffinization, antigen retrieval and endogenous peroxide blocking, the sections (5 μm in thickness) were incubated with primary anti-CD34 antibody (Catalog No. ZM-0046, ZSGB-BIO, Beijing, China), anti-EFNB2 antibody (1:50; Catalog No. HPA008999, Atlas Antibodies, Bromma, Sweden), anti-METAP2 antibody (1:3000; Catalog No. HPA019095, Atlas Antibodies), anti-VIM antibody (Catalog No. ZM-0260, ZSGB-BIO) and anti-MTDH antibody (1:150; Catalog No. ab124789, Abcam, Cambridge, UK).

Techniques: Immunostaining, Immunohistochemical staining, Control, Quantitative RT-PCR, Negative Control, Standard Deviation