rabbit anti-human rankl polyclonal antibody (PeproTech)
Structured Review

Rabbit Anti Human Rankl Polyclonal Antibody, supplied by PeproTech, 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/result/rabbit anti-human rankl polyclonal antibody/product/PeproTech
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "Activated Human T Cells Express Alternative mRNA Transcripts Encoding a Secreted Form of RANKL"
Article Title: Activated Human T Cells Express Alternative mRNA Transcripts Encoding a Secreted Form of RANKL
Journal: Genes and immunity
doi: 10.1038/gene.2013.29
Figure Legend Snippet: A. Color coded schematics showing the exon structure for the human TNFSF11 mRNA transcripts aligned with the known RANKL protein domains. Key: E, Exon; EST, expressed sequence tag; IC, intracellular; TM, transmembrane; EC, extracellular; A +1 TG, translation start site. B. Schematic showing the genomic structure of the human TNFSF11/RANKL locus. Numbering corresponds to the human genomic contig Accession: AL139382. C. Vista genome alignment of the human TNFSF11 genomic locus (identified by exon-intron schematic at top) to rhesus monkey, dog and mouse genomic loci. Shaded areas identify regions where sequence identity across a 50 bp window is 70% or greater. Key: Light blue shading : conservation of untranslated sequences; dark blue shading : conserved coding sequence; pink shading : conserved intron sequence. Location of repeat elements and single nucleotide polymorphisms (SNPs) are marked as indicated in the figure.
Techniques Used: Sequencing
Figure Legend Snippet: A. Semi-quantitative PCR followed by southern hybridization using primers to E1B and E5, shows expression of TNFSF11 Variant 2 in Saos-2 and Jurkat T cells. A second PCR product containing E1B and E2-5 was also amplified. Expression of HPRT is shown as a loading control. B. Western blots showing that the longest open reading frame of TNFSF11 Variant 2 is translated and secreted when expressed as a myc-fusion protein in 293FT cells. Identity of the protein in cell lysates and culture media was confirmed using both an anti-RANKL antibody and anti-myc antibody. C. and D. Conditioned media from 293FT cells transfected with secRANKL vector supports osteoclast differentiation (identified by counting TRAP-positive cells (red staining) with > 3 nuclei which is blocked by inclusion of 200ng/mL OPG. C. Representative results are shown C. Osteoclast quantitation/well (average of 3 wells +/−SD). D. Representative images of each culture condition (the equivalent of 10ng/mL RANKL is shown for secRANKL vector).
Techniques Used: Real-time Polymerase Chain Reaction, Hybridization, Expressing, Variant Assay, Amplification, Control, Western Blot, Transfection, Plasmid Preparation, Staining, Quantitation Assay
Figure Legend Snippet: A. TNFSF11 transcript expression in Jurkat T cells stimulated for 24 hrs with PMA/ionomycin (P/I) with and without cyclosporine A (CsA) pre-treatment. Left panel: representative semi-quantitative RT-PCR results using primers specific for TNFSF11 Variant 2 (E1B-E5) (minimum of 3 biologic repeats). GAPDH is shown as loading control. Right panel: quantitative RT-PCR showing relative expression (GAPDH house keeping gene) of total TNFSF11 expression (n = 3). * p ≤ 0.05. B. TNFSF11 mRNA expression in primary human T cells stimulated for 6 hrs with either anti-CD2/anti-CD3/anti-CD28 conjugated to MACS Bead particles (MACS-ABMB) or P/I with and without CsA pre-treatment. Left panel: representative semi-quantitative RT-PCR using primers specific for TNFSF11 Variant 1 (amplified from E1D-E4) and Transcript Variant 2 (amplified from E1B-E5) (minimum of 3 biologic repeats). GAPDH was used as the housekeeping gene. Right panel: quantitative RT-PCR showing relative expression (GAPDH housekeeping gene) of total TNFSF11 and TNFSF11 Variant 1 expression (n = 3). * and # indicate statistically significant differences (p ≤ 0.05) between indicated conditions for TNFSF11 Variant 1 and total TNFSF11 expression respectively.
Techniques Used: Expressing, Quantitative RT-PCR, Variant Assay, Control, Amplification
Figure Legend Snippet: A. Western Bot showing expression of secreted RANKL protein isoform in Jurkat T cell lysates and culture media with or without PMA/ionomycin (P/I) stimulation. RANKL-GST (a recombinant full-length transmembrane RANKL protein) was run as a control. Cont – control. B. Flow cytometry analysis of surface (membrane-bound) RANKL protein expression (i) Unstimulated MG-63 and (ii) Jurkat T cells, vehicle control or P/I stimulated. C. Flow cytometry analysis of intracellular RANKL protein expression in permeabilized Jurkat T cells treated with or without brefeldin before harvest. (i) Control unstimulated or (ii) PMA/ionomycin stimulated Jurkat T cells without brefeldin treatment (iii) Control unstimulated or (iv) P/I stimulated Jurkat T cells treated with brefeldin.
Techniques Used: Western Blot, Expressing, Recombinant, Control, Flow Cytometry, Membrane
Figure Legend Snippet: Primers
Techniques Used: Sequencing, Variant Assay
