rabbit slc12a2 Search Results


94
ABclonal Biotechnology nkcc1 protein
a Schematic illustration of the functions of siR/RSV@TNP in ChP epithelial cells. Illustration created using Microsoft PowerPoint, incorporating elements (siR/RSV@TNP and SPAK siRNA) adapted from in BioRender. Gao, H. (2025) https://BioRender.com/i60a962 . b The mRNA expression of SPAK after different treatments, n = 4 biological replicates for each group. c Western blot result of SPAK. d Immunofluorescence of SPAK. Scale bar, 20 μm. e Western blot result of SPAK. f , g The mRNA expression of <t>NKCC1</t> and KCNJ13 after different treatments, n = 4 biological replicates for each group respectively. h Western blot result of p-SPAK, n = 3 biological replicates for each group. i Immunofluorescence of pSPAK. Scale bar, 20 μm. All data are presented as mean ± SD. One-way analysis of variance (ANOVA) with Tukey’s multiple comparisons test or Dunnett’s multiple comparisons test were used for the statistical comparison among multiple groups, respectively. Statistical analyses were conducted with a 95% confidence interval, and significance was defined as p < 0.05. Source data are provided as a Source Data file.
Nkcc1 Protein, supplied by ABclonal Biotechnology, 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/rabbit+slc12a2/SLC12A2+Rabbit+pAb/pmc12246246-269-5-19
Average 94 stars, based on 1 article reviews
nkcc1 protein - by Bioz Stars, 2026-10
94/100 stars
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Rabbit anti-Human SLC12A2 Polyclonal Antibody
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SLC12A2 / NKCC1 Rabbit anti-Human Polyclonal (C-Terminus) (Unconjugated) Antibody, (50 µg)
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Rabbit Polyclonal Anti SLC12A2 Antibody
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SLC12A2 / NKCC1 Rabbit anti-Human Polyclonal (Internal) (Unconjugated) Antibody, (50 µg)
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Image Search Results


a Schematic illustration of the functions of siR/RSV@TNP in ChP epithelial cells. Illustration created using Microsoft PowerPoint, incorporating elements (siR/RSV@TNP and SPAK siRNA) adapted from in BioRender. Gao, H. (2025) https://BioRender.com/i60a962 . b The mRNA expression of SPAK after different treatments, n = 4 biological replicates for each group. c Western blot result of SPAK. d Immunofluorescence of SPAK. Scale bar, 20 μm. e Western blot result of SPAK. f , g The mRNA expression of NKCC1 and KCNJ13 after different treatments, n = 4 biological replicates for each group respectively. h Western blot result of p-SPAK, n = 3 biological replicates for each group. i Immunofluorescence of pSPAK. Scale bar, 20 μm. All data are presented as mean ± SD. One-way analysis of variance (ANOVA) with Tukey’s multiple comparisons test or Dunnett’s multiple comparisons test were used for the statistical comparison among multiple groups, respectively. Statistical analyses were conducted with a 95% confidence interval, and significance was defined as p < 0.05. Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: Targeting modulation of the choroid plexus blood-CSF barrier and CSF hypersecretion via lipid nanoparticle-mediated co-delivery of siRNA and resveratrol

doi: 10.1038/s41467-025-61543-1

Figure Lengend Snippet: a Schematic illustration of the functions of siR/RSV@TNP in ChP epithelial cells. Illustration created using Microsoft PowerPoint, incorporating elements (siR/RSV@TNP and SPAK siRNA) adapted from in BioRender. Gao, H. (2025) https://BioRender.com/i60a962 . b The mRNA expression of SPAK after different treatments, n = 4 biological replicates for each group. c Western blot result of SPAK. d Immunofluorescence of SPAK. Scale bar, 20 μm. e Western blot result of SPAK. f , g The mRNA expression of NKCC1 and KCNJ13 after different treatments, n = 4 biological replicates for each group respectively. h Western blot result of p-SPAK, n = 3 biological replicates for each group. i Immunofluorescence of pSPAK. Scale bar, 20 μm. All data are presented as mean ± SD. One-way analysis of variance (ANOVA) with Tukey’s multiple comparisons test or Dunnett’s multiple comparisons test were used for the statistical comparison among multiple groups, respectively. Statistical analyses were conducted with a 95% confidence interval, and significance was defined as p < 0.05. Source data are provided as a Source Data file.

Article Snippet: The expression of SPAK an NKCC1 protein was detected using the Western Blotting analysis, employing specific antibodies for SPAK (ABclonal, A2275, 1:1000) and NKCC1 (Proteintech, 13884-1-AP, 1:1000).

Techniques: Expressing, Western Blot, Immunofluorescence, Comparison