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Bethyl fip1
Fip1, supplied by Bethyl, used in various techniques. Bioz Stars score: 91/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/a301+462a/FIP1+Antibody/pm40629911-54-24-29
Average 91 stars, based on 10 article reviews
fip1 - by Bioz Stars, 2026-09
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Bethyl rabbit α fip1l1
Fig. 1. Heterozygous deletion and missense mutations reduce CPSF6 levels in patients. (A) Deletions spanning CPSF6 (orange box) on chromosome 12q15 iden- tified in eight subjects. Dashed lines indicate the minimal overlapping region, which deleted 99% of CPSF6 (subject 8). Mb, megabases. (B) Schematic of the CPSF6 protein showing the RNA binding domain (RBP; orange), the Arg/Ser-rich domain (R/SD) within the nuclear targeting domain (NTD; turquoise), and the CPSF5-interacting domain (blue). Database searches identified 15 individuals with 13 missense variants (indicated by lollipops), which are plotted here for context, but only subjects 9 to 11 (red) were enrolled in this study. Bottom: Evolutionary alignment shows that the three variants in our subjects affect residues that are conserved from zebrafish to humans and have high pathogenicity scores. See fig. S2 for details of the three splicing variants. (C) Representative Western blot and relative quantification shows that subjects 8 and 11 (the only subjects from whom we obtained fibroblasts) have lower CPSF6, CPSF5, CPSF7, and <t>FIP1L1</t> protein levels than controls. Data were normalized to GAPDH(- glyceraldehyde-3-phosphate dehydrogenase) protein. Data represent means ± SEM from at least four technical and biological replicates compared to healthy age- matched fibroblasts, *P < 0.05, **P < 0.01, and ***P < 0.001.
Rabbit α Fip1l1, supplied by Bethyl, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/a301+462a/FIP1+Antibody/pm36800428-310-39-43
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rabbit α fip1l1 - by Bioz Stars, 2026-09
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Fig. 1. Heterozygous deletion and missense mutations reduce CPSF6 levels in patients. (A) Deletions spanning CPSF6 (orange box) on chromosome 12q15 iden- tified in eight subjects. Dashed lines indicate the minimal overlapping region, which deleted 99% of CPSF6 (subject 8). Mb, megabases. (B) Schematic of the CPSF6 protein showing the RNA binding domain (RBP; orange), the Arg/Ser-rich domain (R/SD) within the nuclear targeting domain (NTD; turquoise), and the CPSF5-interacting domain (blue). Database searches identified 15 individuals with 13 missense variants (indicated by lollipops), which are plotted here for context, but only subjects 9 to 11 (red) were enrolled in this study. Bottom: Evolutionary alignment shows that the three variants in our subjects affect residues that are conserved from zebrafish to humans and have high pathogenicity scores. See fig. S2 for details of the three splicing variants. (C) Representative Western blot and relative quantification shows that subjects 8 and 11 (the only subjects from whom we obtained fibroblasts) have lower CPSF6, CPSF5, CPSF7, and FIP1L1 protein levels than controls. Data were normalized to GAPDH(- glyceraldehyde-3-phosphate dehydrogenase) protein. Data represent means ± SEM from at least four technical and biological replicates compared to healthy age- matched fibroblasts, *P < 0.05, **P < 0.01, and ***P < 0.001.

Journal: Science advances

Article Title: Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites.

doi: 10.1126/sciadv.ade4814

Figure Lengend Snippet: Fig. 1. Heterozygous deletion and missense mutations reduce CPSF6 levels in patients. (A) Deletions spanning CPSF6 (orange box) on chromosome 12q15 iden- tified in eight subjects. Dashed lines indicate the minimal overlapping region, which deleted 99% of CPSF6 (subject 8). Mb, megabases. (B) Schematic of the CPSF6 protein showing the RNA binding domain (RBP; orange), the Arg/Ser-rich domain (R/SD) within the nuclear targeting domain (NTD; turquoise), and the CPSF5-interacting domain (blue). Database searches identified 15 individuals with 13 missense variants (indicated by lollipops), which are plotted here for context, but only subjects 9 to 11 (red) were enrolled in this study. Bottom: Evolutionary alignment shows that the three variants in our subjects affect residues that are conserved from zebrafish to humans and have high pathogenicity scores. See fig. S2 for details of the three splicing variants. (C) Representative Western blot and relative quantification shows that subjects 8 and 11 (the only subjects from whom we obtained fibroblasts) have lower CPSF6, CPSF5, CPSF7, and FIP1L1 protein levels than controls. Data were normalized to GAPDH(- glyceraldehyde-3-phosphate dehydrogenase) protein. Data represent means ± SEM from at least four technical and biological replicates compared to healthy age- matched fibroblasts, *P < 0.05, **P < 0.01, and ***P < 0.001.

Article Snippet: Antibodies used for all the Western blot experiments were as follows: rabbit α-CPSF6 [1:1000 (Bethyl Laboratories, TX, catalog no. A301-356A)], mouse α-NUDT21 (2203C3) [1:500 (Santa Cruz, TX, catalog no. sc-81109)], mouse α-CPSF7 [1:500 (Santa Cruz, TX, catalog no. sc-393880)], rabbit α-FIP1L1 [1:500 (A301461A, Bethyl Laboratories, TX)], rabbit α-SCAF4 [1:1000 (Bethyl Laboratories, TX, catalog no. A303-951A)], and mouse α–glyceraldehyde-3-phosphate dehydrogenase [1:10,000 (Millipore, catalog no. CB1001)]. qPCR in human cells and zebrafish For human cells, we collected cells as described above for Western blot.

Techniques: RNA Binding Assay, Western Blot, Quantitative Proteomics