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ib4  (Vector Laboratories)


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    Structured Review

    Vector Laboratories ib4
    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and <t>IB4</t> (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
    Ib4, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 323 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Tmem45b modulates itch via endoplasmic reticulum calcium regulation"

    Article Title: Tmem45b modulates itch via endoplasmic reticulum calcium regulation

    Journal: Frontiers in Physiology

    doi: 10.3389/fphys.2025.1708686

    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and IB4 (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
    Figure Legend Snippet: Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and IB4 (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.

    Techniques Used: Immunostaining, Expressing, RNAscope, In Situ Hybridization



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    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and <t>IB4</t> (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
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    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and <t>IB4</t> (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
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    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and <t>IB4</t> (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
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    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and <t>IB4</t> (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
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    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and <t>IB4</t> (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
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    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and <t>IB4</t> (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.
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    Selection of homozygously edited cells based on highest surrogate reporter expression. ( A ) Schematic of selection strategy using version 2.1- eGFP (V2.1G), a nonintegrated surrogate reporter system. PFFs were cotransfected with V2.1G, Cas9, and sgRNA plasmid, whereas the control group was only transfected with the V2.1G plasmid. FACS analysis revealed varying intensities of FITC expression among the cells. (H) The highest FITC intensity population, (M) the middle FITC intensity population, (L) the lower FITC intensity population, and (N) the negative FITC intensity population. ( B ) Correlation between genome editing efficiency and FITC intensity of endogenous targeting in PFFs. ( C ) Representative Sanger sequences of CMAH target site in wild-type cells, homozygous cell clones, and cell pools selected by V2.1G. ( D ) FACS analysis of GGTA1 targeting in PFF pools detection by <t>IB4</t> <t>lectin</t> staining. ( E ) Western blot analysis of USE1-targeted Vero E6 cell pools with middle and high FITC intensity, respectively.
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    Selection of homozygously edited cells based on highest surrogate reporter expression. ( A ) Schematic of selection strategy using version 2.1- eGFP (V2.1G), a nonintegrated surrogate reporter system. PFFs were cotransfected with V2.1G, Cas9, and sgRNA plasmid, whereas the control group was only transfected with the V2.1G plasmid. FACS analysis revealed varying intensities of FITC expression among the cells. (H) The highest FITC intensity population, (M) the middle FITC intensity population, (L) the lower FITC intensity population, and (N) the negative FITC intensity population. ( B ) Correlation between genome editing efficiency and FITC intensity of endogenous targeting in PFFs. ( C ) Representative Sanger sequences of CMAH target site in wild-type cells, homozygous cell clones, and cell pools selected by V2.1G. ( D ) FACS analysis of GGTA1 targeting in PFF pools detection by <t>IB4</t> <t>lectin</t> staining. ( E ) Western blot analysis of USE1-targeted Vero E6 cell pools with middle and high FITC intensity, respectively.
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    Selection of homozygously edited cells based on highest surrogate reporter expression. ( A ) Schematic of selection strategy using version 2.1- eGFP (V2.1G), a nonintegrated surrogate reporter system. PFFs were cotransfected with V2.1G, Cas9, and sgRNA plasmid, whereas the control group was only transfected with the V2.1G plasmid. FACS analysis revealed varying intensities of FITC expression among the cells. (H) The highest FITC intensity population, (M) the middle FITC intensity population, (L) the lower FITC intensity population, and (N) the negative FITC intensity population. ( B ) Correlation between genome editing efficiency and FITC intensity of endogenous targeting in PFFs. ( C ) Representative Sanger sequences of CMAH target site in wild-type cells, homozygous cell clones, and cell pools selected by V2.1G. ( D ) FACS analysis of GGTA1 targeting in PFF pools detection by <t>IB4</t> <t>lectin</t> staining. ( E ) Western blot analysis of USE1-targeted Vero E6 cell pools with middle and high FITC intensity, respectively.
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    Image Search Results


    Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and IB4 (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.

    Journal: Frontiers in Physiology

    Article Title: Tmem45b modulates itch via endoplasmic reticulum calcium regulation

    doi: 10.3389/fphys.2025.1708686

    Figure Lengend Snippet: Tmem45b is primarily expressed in itch-sensing neurons. (A) Immunostaining results show the expression of Tmem45b (green), CGRP (red), and NF200 (red). (B) Immunostaining results show the co-expression of Tmem45b (green) and IB4 (red). (C) Statistical analysis shows the proportion of Tmem45b + IB4 + . (D) scRNA-seq (10x Genomics) analysis identified 16 subtypes of DRG neurons. Gene annotations for these 16 neuron types are shown in the right panel. Tmem45b is predominantly enriched in neurons positive for Mrgprd, Mrgpra3, Nppb , and Th . (E) RNAscope in situ hybridization shows co-localization among Tmem45b (green), Mrgprd (red) , Mrgpra3 (red), and Nppb (red). Immunostaining results show that Tmem45b (green) is co-expressed with Th (red). Arrows indicate co-expressing cells. Scale bar, 20 μm. (F) Proportions of Mrgprd + , Mrgpra3 + , Nppb + , and Th + neurons among Tmem45b + DRG neurons. DRG was obtained from at least 3 mice.

    Article Snippet: Antibodies used in this study: GM130 (BD, 610822), Th (Millipore, AB1542), IB4 (Vector, FL-1201-.5), Tuj1 (Starter, SDT-251-28), CGRP (Dia Sorin, 24112), NF200 (CST, 2836S), PDI (Santa Cruz, SC-20132), Calnexin (Abcam, ab112995), Serca1 (Proteintech, 22361-1-AP), mitochondria-tracer (Beyotime, C1048), TGN38 (Bio-Rad, AHP499G), GFAP (Millipore, MAB3402), IBA1 (Abcam, ab5076).

    Techniques: Immunostaining, Expressing, RNAscope, In Situ Hybridization

    Selection of homozygously edited cells based on highest surrogate reporter expression. ( A ) Schematic of selection strategy using version 2.1- eGFP (V2.1G), a nonintegrated surrogate reporter system. PFFs were cotransfected with V2.1G, Cas9, and sgRNA plasmid, whereas the control group was only transfected with the V2.1G plasmid. FACS analysis revealed varying intensities of FITC expression among the cells. (H) The highest FITC intensity population, (M) the middle FITC intensity population, (L) the lower FITC intensity population, and (N) the negative FITC intensity population. ( B ) Correlation between genome editing efficiency and FITC intensity of endogenous targeting in PFFs. ( C ) Representative Sanger sequences of CMAH target site in wild-type cells, homozygous cell clones, and cell pools selected by V2.1G. ( D ) FACS analysis of GGTA1 targeting in PFF pools detection by IB4 lectin staining. ( E ) Western blot analysis of USE1-targeted Vero E6 cell pools with middle and high FITC intensity, respectively.

    Journal: Genome Research

    Article Title: Homozygous editing of multiple genes for accelerated generation of xenotransplantation pigs

    doi: 10.1101/gr.279709.124

    Figure Lengend Snippet: Selection of homozygously edited cells based on highest surrogate reporter expression. ( A ) Schematic of selection strategy using version 2.1- eGFP (V2.1G), a nonintegrated surrogate reporter system. PFFs were cotransfected with V2.1G, Cas9, and sgRNA plasmid, whereas the control group was only transfected with the V2.1G plasmid. FACS analysis revealed varying intensities of FITC expression among the cells. (H) The highest FITC intensity population, (M) the middle FITC intensity population, (L) the lower FITC intensity population, and (N) the negative FITC intensity population. ( B ) Correlation between genome editing efficiency and FITC intensity of endogenous targeting in PFFs. ( C ) Representative Sanger sequences of CMAH target site in wild-type cells, homozygous cell clones, and cell pools selected by V2.1G. ( D ) FACS analysis of GGTA1 targeting in PFF pools detection by IB4 lectin staining. ( E ) Western blot analysis of USE1-targeted Vero E6 cell pools with middle and high FITC intensity, respectively.

    Article Snippet: The following lectins and antibodies were used for staining: IB4 lectin (Vector FL-1201, 1:50 dilution), DBA lectin (Vector FL-1031, 1:50 dilution), AntiNeuGC (BioLegend 146901, 1:50 dilution), and thrombomodulin antibody (Abmart T55279, 1:100 dilution).

    Techniques: Selection, Expressing, Plasmid Preparation, Control, Transfection, Clone Assay, Staining, Western Blot