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arpp19  (Proteintech)


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    Structured Review

    Proteintech arpp19
    RT‐qPCR showing the mRNA expression of (A) ZNF207 , (B) ZNRF1 , (C) RGS1 , (D) <t>ARPP19</t> , (E) CXCR4 , and (F) CTLA4 in paracancerous (principal component, PC) tissues ( n = 10) and gastric cancer (GC) samples ( n = 10). * p < 0.05, ** p < 0.01, *** p < 0.001.
    Arpp19, supplied by Proteintech, 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/arpp+19/pmc12806102-183-23-24?v=Proteintech
    Average 94 stars, based on 1 article reviews
    arpp19 - by Bioz Stars, 2026-08
    94/100 stars

    Images

    1) Product Images from "Metabolic‐immune interactions in gastric cancer T cells: A single‐cell atlas for prognostic biomarker identification"

    Article Title: Metabolic‐immune interactions in gastric cancer T cells: A single‐cell atlas for prognostic biomarker identification

    Journal: Quantitative Biology

    doi: 10.1002/qub2.70027

    RT‐qPCR showing the mRNA expression of (A) ZNF207 , (B) ZNRF1 , (C) RGS1 , (D) ARPP19 , (E) CXCR4 , and (F) CTLA4 in paracancerous (principal component, PC) tissues ( n = 10) and gastric cancer (GC) samples ( n = 10). * p < 0.05, ** p < 0.01, *** p < 0.001.
    Figure Legend Snippet: RT‐qPCR showing the mRNA expression of (A) ZNF207 , (B) ZNRF1 , (C) RGS1 , (D) ARPP19 , (E) CXCR4 , and (F) CTLA4 in paracancerous (principal component, PC) tissues ( n = 10) and gastric cancer (GC) samples ( n = 10). * p < 0.05, ** p < 0.01, *** p < 0.001.

    Techniques Used: Quantitative RT-PCR, Expressing

    Immunohistochemical staining of target genes (A) ZNF207 , (B) ARPP19 , (C) ZNRF1 , (D) CXCR4 , (E) RGS1 , and (F) CTLA4 expression profiles in gastric cancer specimens and their corresponding adjacent normal gastric tissues. Brown chromogenic staining reveals positive protein expression. Blue counterstaining visualizes cell nuclei. Scale bar: 100 μm.
    Figure Legend Snippet: Immunohistochemical staining of target genes (A) ZNF207 , (B) ARPP19 , (C) ZNRF1 , (D) CXCR4 , (E) RGS1 , and (F) CTLA4 expression profiles in gastric cancer specimens and their corresponding adjacent normal gastric tissues. Brown chromogenic staining reveals positive protein expression. Blue counterstaining visualizes cell nuclei. Scale bar: 100 μm.

    Techniques Used: Immunohistochemical staining, Staining, Expressing



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    Image Search Results


    RT‐qPCR showing the mRNA expression of (A) ZNF207 , (B) ZNRF1 , (C) RGS1 , (D) ARPP19 , (E) CXCR4 , and (F) CTLA4 in paracancerous (principal component, PC) tissues ( n = 10) and gastric cancer (GC) samples ( n = 10). * p < 0.05, ** p < 0.01, *** p < 0.001.

    Journal: Quantitative Biology

    Article Title: Metabolic‐immune interactions in gastric cancer T cells: A single‐cell atlas for prognostic biomarker identification

    doi: 10.1002/qub2.70027

    Figure Lengend Snippet: RT‐qPCR showing the mRNA expression of (A) ZNF207 , (B) ZNRF1 , (C) RGS1 , (D) ARPP19 , (E) CXCR4 , and (F) CTLA4 in paracancerous (principal component, PC) tissues ( n = 10) and gastric cancer (GC) samples ( n = 10). * p < 0.05, ** p < 0.01, *** p < 0.001.

    Article Snippet: Immunohistochemical staining was then carried out using primary antibodies targeting RGS1 (Sigma, HPA028453), CXCR4 (Cell Signaling Technology, #97680), CTLA4 (Cell Signaling Technology, #53560), ARPP19 (Proteintech, 11678‐1‐AP), ZNRF1 (LSBio, LS‐C809970), and ZNF207 (Invitrogen, PA5‐53535).

    Techniques: Quantitative RT-PCR, Expressing

    Immunohistochemical staining of target genes (A) ZNF207 , (B) ARPP19 , (C) ZNRF1 , (D) CXCR4 , (E) RGS1 , and (F) CTLA4 expression profiles in gastric cancer specimens and their corresponding adjacent normal gastric tissues. Brown chromogenic staining reveals positive protein expression. Blue counterstaining visualizes cell nuclei. Scale bar: 100 μm.

    Journal: Quantitative Biology

    Article Title: Metabolic‐immune interactions in gastric cancer T cells: A single‐cell atlas for prognostic biomarker identification

    doi: 10.1002/qub2.70027

    Figure Lengend Snippet: Immunohistochemical staining of target genes (A) ZNF207 , (B) ARPP19 , (C) ZNRF1 , (D) CXCR4 , (E) RGS1 , and (F) CTLA4 expression profiles in gastric cancer specimens and their corresponding adjacent normal gastric tissues. Brown chromogenic staining reveals positive protein expression. Blue counterstaining visualizes cell nuclei. Scale bar: 100 μm.

    Article Snippet: Immunohistochemical staining was then carried out using primary antibodies targeting RGS1 (Sigma, HPA028453), CXCR4 (Cell Signaling Technology, #97680), CTLA4 (Cell Signaling Technology, #53560), ARPP19 (Proteintech, 11678‐1‐AP), ZNRF1 (LSBio, LS‐C809970), and ZNF207 (Invitrogen, PA5‐53535).

    Techniques: Immunohistochemical staining, Staining, Expressing

    BMSCs derived exosomes increased the level of XIST in osteosarcoma cells. A The exosomes from BMSCs analyzed by TEM; B The levels of exosome markers CD9, CD63, CD81 and endoplasmic reticulum marker calnexin detected by western blot (n = 3); C PKH26-labeled exosomes internalized by osteosarcoma cellline MG63 and 143B; D qRT-PCR analysis of the level of XIST in osteosarcoma cell lines MG63 and 143B treated with different concentrations of exosomes from BMSCs (n = 3); E FISH results to observe the level and localization of XIST in osteosarcoma cell lines MG63 and 143B after treatment with BMSCs derived exosomes. ** represents p < 0.01

    Journal: Cancer Cell International

    Article Title: LncRNA XIST from the bone marrow mesenchymal stem cell derived exosome promotes osteosarcoma growth and metastasis through miR-655/ACLY signal

    doi: 10.1186/s12935-022-02746-0

    Figure Lengend Snippet: BMSCs derived exosomes increased the level of XIST in osteosarcoma cells. A The exosomes from BMSCs analyzed by TEM; B The levels of exosome markers CD9, CD63, CD81 and endoplasmic reticulum marker calnexin detected by western blot (n = 3); C PKH26-labeled exosomes internalized by osteosarcoma cellline MG63 and 143B; D qRT-PCR analysis of the level of XIST in osteosarcoma cell lines MG63 and 143B treated with different concentrations of exosomes from BMSCs (n = 3); E FISH results to observe the level and localization of XIST in osteosarcoma cell lines MG63 and 143B after treatment with BMSCs derived exosomes. ** represents p < 0.01

    Article Snippet: The PVDF membrane was incubated with primary antibodies diluted with blocking solution overnight at 4°C respectively (GAPDH, Abcam, ab8245; Lamin B1, Abcam, ab16048; β-catenin, Abcam, ab32572; CD9, Abcam, ab263019; CD63, Abcam, ab134045; CD81, Abcam, ab79559; calnexin, CST, 2679; ARPP19, Affinity, DF9325; TOB1, ProteintechGroup, Inc, 14915-1-AP; ACLY, Abcam, ab40793. the dilution ratio was 1:1000), and the corresponding HRP labeled secondary antibody (HRP labeled Sheep anti-mouse secondary antibody, Wuhan Boster Biological Technology., Ltd., BA1051; HRP labeled Sheep anti-rabbit secondary antibody, Wuhan Boster Biological Technology., Ltd., BA1054; the dilution ratio was 1:5000) was diluted with the blocking solution and the PVDF membrane was incubated at room temperature.

    Techniques: Derivative Assay, Marker, Western Blot, Labeling, Quantitative RT-PCR