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anti trka  (Alomone Labs)


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    Structured Review

    Alomone Labs anti trka
    (A) Heatmap analysis on the samples from 2-step N1 and N1-I, showing the expression of indicated markers. Transcript expression values (TPM) were log10-transformed, and Z-scores were calculated. (B) Representative images showing neuronal morphology at different stages of differentiation under the 2-step N1-I, namely iPruriceptor, protocol on day12, 17, 21. Scale bars indicate 100μm. (C) Immunofluorescence staining of indicated markers on the induced neurons under iPruriceptor protocol on day 28. Scale bars indicate 50μm. The table shows the proportion of induced neurons under iPruriceptor protocol expressing the indicated markers on day 28. The percentages <t>of</t> <t>TRPV1-,</t> <t>TrkA-,</t> RET-, IL31ra-, or OSMR-positive cells among the β3 tubulin–positive population, which were stained simultaneously with each described marker, were shown.
    Anti Trka, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ant-018/bio_rxiv__2025__06__11__659208-263-28-30?v=Alomone+Labs
    Average 93 stars, based on 17 article reviews
    anti trka - by Bioz Stars, 2026-07
    93/100 stars

    Images

    1) Product Images from "Induction of Human Pruriceptors from Pluripotent Stem Cells via Transcription Factors"

    Article Title: Induction of Human Pruriceptors from Pluripotent Stem Cells via Transcription Factors

    Journal: bioRxiv

    doi: 10.1101/2025.06.11.659208

    (A) Heatmap analysis on the samples from 2-step N1 and N1-I, showing the expression of indicated markers. Transcript expression values (TPM) were log10-transformed, and Z-scores were calculated. (B) Representative images showing neuronal morphology at different stages of differentiation under the 2-step N1-I, namely iPruriceptor, protocol on day12, 17, 21. Scale bars indicate 100μm. (C) Immunofluorescence staining of indicated markers on the induced neurons under iPruriceptor protocol on day 28. Scale bars indicate 50μm. The table shows the proportion of induced neurons under iPruriceptor protocol expressing the indicated markers on day 28. The percentages of TRPV1-, TrkA-, RET-, IL31ra-, or OSMR-positive cells among the β3 tubulin–positive population, which were stained simultaneously with each described marker, were shown.
    Figure Legend Snippet: (A) Heatmap analysis on the samples from 2-step N1 and N1-I, showing the expression of indicated markers. Transcript expression values (TPM) were log10-transformed, and Z-scores were calculated. (B) Representative images showing neuronal morphology at different stages of differentiation under the 2-step N1-I, namely iPruriceptor, protocol on day12, 17, 21. Scale bars indicate 100μm. (C) Immunofluorescence staining of indicated markers on the induced neurons under iPruriceptor protocol on day 28. Scale bars indicate 50μm. The table shows the proportion of induced neurons under iPruriceptor protocol expressing the indicated markers on day 28. The percentages of TRPV1-, TrkA-, RET-, IL31ra-, or OSMR-positive cells among the β3 tubulin–positive population, which were stained simultaneously with each described marker, were shown.

    Techniques Used: Expressing, Transformation Assay, Immunofluorescence, Staining, Marker



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    (A) Heatmap analysis on the samples from 2-step N1 and N1-I, showing the expression of indicated markers. Transcript expression values (TPM) were log10-transformed, and Z-scores were calculated. (B) Representative images showing neuronal morphology at different stages of differentiation under the 2-step N1-I, namely iPruriceptor, protocol on day12, 17, 21. Scale bars indicate 100μm. (C) Immunofluorescence staining of indicated markers on the induced neurons under iPruriceptor protocol on day 28. Scale bars indicate 50μm. The table shows the proportion of induced neurons under iPruriceptor protocol expressing the indicated markers on day 28. The percentages <t>of</t> <t>TRPV1-,</t> <t>TrkA-,</t> RET-, IL31ra-, or OSMR-positive cells among the β3 tubulin–positive population, which were stained simultaneously with each described marker, were shown.
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    Image Search Results


    (A) Heatmap analysis on the samples from 2-step N1 and N1-I, showing the expression of indicated markers. Transcript expression values (TPM) were log10-transformed, and Z-scores were calculated. (B) Representative images showing neuronal morphology at different stages of differentiation under the 2-step N1-I, namely iPruriceptor, protocol on day12, 17, 21. Scale bars indicate 100μm. (C) Immunofluorescence staining of indicated markers on the induced neurons under iPruriceptor protocol on day 28. Scale bars indicate 50μm. The table shows the proportion of induced neurons under iPruriceptor protocol expressing the indicated markers on day 28. The percentages of TRPV1-, TrkA-, RET-, IL31ra-, or OSMR-positive cells among the β3 tubulin–positive population, which were stained simultaneously with each described marker, were shown.

    Journal: bioRxiv

    Article Title: Induction of Human Pruriceptors from Pluripotent Stem Cells via Transcription Factors

    doi: 10.1101/2025.06.11.659208

    Figure Lengend Snippet: (A) Heatmap analysis on the samples from 2-step N1 and N1-I, showing the expression of indicated markers. Transcript expression values (TPM) were log10-transformed, and Z-scores were calculated. (B) Representative images showing neuronal morphology at different stages of differentiation under the 2-step N1-I, namely iPruriceptor, protocol on day12, 17, 21. Scale bars indicate 100μm. (C) Immunofluorescence staining of indicated markers on the induced neurons under iPruriceptor protocol on day 28. Scale bars indicate 50μm. The table shows the proportion of induced neurons under iPruriceptor protocol expressing the indicated markers on day 28. The percentages of TRPV1-, TrkA-, RET-, IL31ra-, or OSMR-positive cells among the β3 tubulin–positive population, which were stained simultaneously with each described marker, were shown.

    Article Snippet: The cells were then incubated overnight at 4°C with the following primary antibodies diluted in blocking buffer: [anti-Tubb3 (Biolegend, 801201, 1:1000), anti-MAP2 (Abcam, AB5392,1:20000), anti-TRPV1 (Almone Lab, ACC-030,1:200), anti- Trka (Almone Lab, ANT-018, 1:200), anti-IL31RA (Abcam, AB113498, 1:200), anti- OSMR (LSBio, LS-B11477-50, 1:200), anti-RET (Novus biologicals, AF1485, 1:200)].

    Techniques: Expressing, Transformation Assay, Immunofluorescence, Staining, Marker