plasmid map and coding sequence for recombinant fabp1 Search Results


rabbit monoclonal anti got2  (Novus Biologicals)
90
Novus Biologicals rabbit monoclonal anti got2
KEY RESOURCES TABLE
Rabbit Monoclonal Anti Got2, supplied by Novus Biologicals, 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/plasmid+map+and+coding+sequence+for+recombinant+fabp1/GOT2+Antibody+(4J7O3)/pmc07573785-2-0-4
Average 90 stars, based on 1 article reviews
rabbit monoclonal anti got2 - by Bioz Stars, 2026-09
90/100 stars
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fapb1  (R&D Systems)
93
R&D Systems fapb1
Scheme of 24 h Bmp treatment of freshly isolated crypts including debris removal step prior to the treatment. Brightfield images of freshly isolated crypts treated with 24 h with indicated Bmp (Scale bar, 200 μm). Expression of generic Bmp target genes Id1, Id2 and Id3 upon 24 h Bmp treatment. (Graphs show normalized counts determined by RNAseq, n = at least 3 for each treatment and error bars denote SD). The expression of indicated villus centre genes and villus tip genes throughout the villus. Dot plot: size of the dot represents the percentage of the cells expressing the transcript and colour indicates the expression level. Used datasets: GSM2644349 and GSM2644350 (Yan et al , ; Data ref: Yan et al , ) reanalysed by Moor et al , Data ref: Moor et al . The expression of c‐Maf, the master regulator of lipid metabolism and uptake, is initiated preferentially by Bmp4. (Graph shows normalized counts determined by RNAseq, n = at least 3 for each treatment, timepoint: 24 h, error bars denote SD). Fabp1 and Fabp2 proteins connected to lipid uptake are expressed upon Bmp4 treatment. Immunoblot of freshly established organoids treated for 48 h as indicated by Bmp2 (500 ng/ml) or Bmp4 (500 ng/ml). Ada is a protein involved in purine metabolism that is expressed at the villus tip. All proteins are expressed after Bmp treatment, but <t>Fapb1</t> and Fabp2 are specifically regulated by Bmp4. qRT–PCR for villus centre genes and villus tip genes in freshly isolated crypts cultivated 24 h in Bmp2 (500 ng/ml) and Bmp4 (500 ng/ml). (Expression levels normalized to ubiquitin B (Ubb), untreated parallel set as 1, each dot represents one technical replicate of one representative experiment, and error bars show SD).
Fapb1, supplied by R&D Systems, 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/plasmid+map+and+coding+sequence+for+recombinant+fabp1/Human%2FMouse%2FRat+FABP1%2FL-FABP+Antibody/pmc10481656-18-0-4
Average 93 stars, based on 1 article reviews
fapb1 - by Bioz Stars, 2026-09
93/100 stars
  Buy from Supplier
lotus tetragonolobus lectin  (Vector Laboratories)
96
Vector Laboratories lotus tetragonolobus lectin
Circulating FABP1 is reabsorbed by PTECs. (A) Serum FABP1 levels were elevated by BLN but not by ULN. Blood was collected from the retro‐orbital plexus 12 h after surgery to measure the serum levels of creatinine and FABP1 ( n = 5). *** p < 0.001. BLN, bilateral nephrectomy; ULN, unilateral nephrectomy. (B) The kidney was isolated 10, 30, and 60 min after intravenous injection of recombinant human FABP1 (rFABP1) for subsequent immunohistochemistry. Scale bar = 500 μm. (C, D) The kidney was isolated 10 min after intravenous injection of Alexa Fluor 647 (AF647)‐rFABP1 for immunofluorescence. Scale bar = 100 μm. (C) Injected AF647‐rFABP1 was detected by anti‐FABP1 antibody (red) and AF647 (purple). (D) Higher magnification. AF647‐rFABP1 (red); lotus <t>tetragonolobus</t> <t>lectin</t> (LTL), a marker for brush border of PTECs (green); DAPI, 4',6‐diamidino‐2‐phenylindole, a marker for nuclei (blue).
Lotus Tetragonolobus Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/plasmid+map+and+coding+sequence+for+recombinant+fabp1/Fluorescein+labeled+Lotus+Tetragonolobus+Lectin+(LTL)/pmc09292749-63-6-10
Average 96 stars, based on 1 article reviews
lotus tetragonolobus lectin - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier

Image Search Results


KEY RESOURCES TABLE

Journal: Cell reports

Article Title: Respiratory Supercomplexes Promote Mitochondrial Efficiency and Growth in Severely Hypoxic Pancreatic Cancer

doi: 10.1016/j.celrep.2020.108231

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: Rabbit monoclonal anti-GOT2 , Novus Biologicals , Cat#NBPI-47469; Lot#160630; RRID:AB_10010421.

Techniques: Plasmid Preparation, Virus, Recombinant, Clinical Proteomics, Membrane, Protease Inhibitor, Avidin-Biotin Assay, Fractionation, Software

Scheme of 24 h Bmp treatment of freshly isolated crypts including debris removal step prior to the treatment. Brightfield images of freshly isolated crypts treated with 24 h with indicated Bmp (Scale bar, 200 μm). Expression of generic Bmp target genes Id1, Id2 and Id3 upon 24 h Bmp treatment. (Graphs show normalized counts determined by RNAseq, n = at least 3 for each treatment and error bars denote SD). The expression of indicated villus centre genes and villus tip genes throughout the villus. Dot plot: size of the dot represents the percentage of the cells expressing the transcript and colour indicates the expression level. Used datasets: GSM2644349 and GSM2644350 (Yan et al , ; Data ref: Yan et al , ) reanalysed by Moor et al , Data ref: Moor et al . The expression of c‐Maf, the master regulator of lipid metabolism and uptake, is initiated preferentially by Bmp4. (Graph shows normalized counts determined by RNAseq, n = at least 3 for each treatment, timepoint: 24 h, error bars denote SD). Fabp1 and Fabp2 proteins connected to lipid uptake are expressed upon Bmp4 treatment. Immunoblot of freshly established organoids treated for 48 h as indicated by Bmp2 (500 ng/ml) or Bmp4 (500 ng/ml). Ada is a protein involved in purine metabolism that is expressed at the villus tip. All proteins are expressed after Bmp treatment, but Fapb1 and Fabp2 are specifically regulated by Bmp4. qRT–PCR for villus centre genes and villus tip genes in freshly isolated crypts cultivated 24 h in Bmp2 (500 ng/ml) and Bmp4 (500 ng/ml). (Expression levels normalized to ubiquitin B (Ubb), untreated parallel set as 1, each dot represents one technical replicate of one representative experiment, and error bars show SD).

Journal: EMBO Reports

Article Title: Terminal differentiation of villus tip enterocytes is governed by distinct Tgfβ superfamily members

doi: 10.15252/embr.202256454

Figure Lengend Snippet: Scheme of 24 h Bmp treatment of freshly isolated crypts including debris removal step prior to the treatment. Brightfield images of freshly isolated crypts treated with 24 h with indicated Bmp (Scale bar, 200 μm). Expression of generic Bmp target genes Id1, Id2 and Id3 upon 24 h Bmp treatment. (Graphs show normalized counts determined by RNAseq, n = at least 3 for each treatment and error bars denote SD). The expression of indicated villus centre genes and villus tip genes throughout the villus. Dot plot: size of the dot represents the percentage of the cells expressing the transcript and colour indicates the expression level. Used datasets: GSM2644349 and GSM2644350 (Yan et al , ; Data ref: Yan et al , ) reanalysed by Moor et al , Data ref: Moor et al . The expression of c‐Maf, the master regulator of lipid metabolism and uptake, is initiated preferentially by Bmp4. (Graph shows normalized counts determined by RNAseq, n = at least 3 for each treatment, timepoint: 24 h, error bars denote SD). Fabp1 and Fabp2 proteins connected to lipid uptake are expressed upon Bmp4 treatment. Immunoblot of freshly established organoids treated for 48 h as indicated by Bmp2 (500 ng/ml) or Bmp4 (500 ng/ml). Ada is a protein involved in purine metabolism that is expressed at the villus tip. All proteins are expressed after Bmp treatment, but Fapb1 and Fabp2 are specifically regulated by Bmp4. qRT–PCR for villus centre genes and villus tip genes in freshly isolated crypts cultivated 24 h in Bmp2 (500 ng/ml) and Bmp4 (500 ng/ml). (Expression levels normalized to ubiquitin B (Ubb), untreated parallel set as 1, each dot represents one technical replicate of one representative experiment, and error bars show SD).

Article Snippet: Fapb1 (goat, polyclonal) , R&DSystems , AF1565.

Techniques: Isolation, Expressing, Western Blot, Quantitative RT-PCR

Journal: EMBO Reports

Article Title: Terminal differentiation of villus tip enterocytes is governed by distinct Tgfβ superfamily members

doi: 10.15252/embr.202256454

Figure Lengend Snippet:

Article Snippet: Fapb1 (goat, polyclonal) , R&DSystems , AF1565.

Techniques: Generated, Recombinant, Expressing, Plasmid Preparation, Transduction, Sequencing, shRNA, Gentle, Software, Positive Control, Negative Control, SYBR Green Assay, Activity Assay

Circulating FABP1 is reabsorbed by PTECs. (A) Serum FABP1 levels were elevated by BLN but not by ULN. Blood was collected from the retro‐orbital plexus 12 h after surgery to measure the serum levels of creatinine and FABP1 ( n = 5). *** p < 0.001. BLN, bilateral nephrectomy; ULN, unilateral nephrectomy. (B) The kidney was isolated 10, 30, and 60 min after intravenous injection of recombinant human FABP1 (rFABP1) for subsequent immunohistochemistry. Scale bar = 500 μm. (C, D) The kidney was isolated 10 min after intravenous injection of Alexa Fluor 647 (AF647)‐rFABP1 for immunofluorescence. Scale bar = 100 μm. (C) Injected AF647‐rFABP1 was detected by anti‐FABP1 antibody (red) and AF647 (purple). (D) Higher magnification. AF647‐rFABP1 (red); lotus tetragonolobus lectin (LTL), a marker for brush border of PTECs (green); DAPI, 4',6‐diamidino‐2‐phenylindole, a marker for nuclei (blue).

Journal: The Journal of Pathology

Article Title: Urinary FABP1 is a biomarker for impaired proximal tubular protein reabsorption and is synergistically enhanced by concurrent liver injury

doi: 10.1002/path.5775

Figure Lengend Snippet: Circulating FABP1 is reabsorbed by PTECs. (A) Serum FABP1 levels were elevated by BLN but not by ULN. Blood was collected from the retro‐orbital plexus 12 h after surgery to measure the serum levels of creatinine and FABP1 ( n = 5). *** p < 0.001. BLN, bilateral nephrectomy; ULN, unilateral nephrectomy. (B) The kidney was isolated 10, 30, and 60 min after intravenous injection of recombinant human FABP1 (rFABP1) for subsequent immunohistochemistry. Scale bar = 500 μm. (C, D) The kidney was isolated 10 min after intravenous injection of Alexa Fluor 647 (AF647)‐rFABP1 for immunofluorescence. Scale bar = 100 μm. (C) Injected AF647‐rFABP1 was detected by anti‐FABP1 antibody (red) and AF647 (purple). (D) Higher magnification. AF647‐rFABP1 (red); lotus tetragonolobus lectin (LTL), a marker for brush border of PTECs (green); DAPI, 4',6‐diamidino‐2‐phenylindole, a marker for nuclei (blue).

Article Snippet: Immunofluorescence analysis was performed with fluorescein‐labeled lotus tetragonolobus lectin (LTL; Vector Laboratories, Burlingame, CA, USA), anti‐FABP1 antibody (Cell Signaling Technology, Inc, Danvers, MA, USA), and AF555‐labeled anti‐rabbit IgG (Thermo Fisher Scientific).

Techniques: Isolation, Injection, Recombinant, Immunohistochemistry, Immunofluorescence, Marker