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gus staining solution  (Gold Biotechnology Inc)


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    Structured Review

    Gold Biotechnology Inc gus staining solution
    <t>Histochemical</t> <t>staining</t> of translational fusion constructs (designs in which a promoter drives the expression of a target gene coding sequence translationally fused to <t>GUS,</t> thereby producing a single fusion protein). Scale bars are 5 mm.
    Gus Staining Solution, supplied by Gold Biotechnology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gus+staining+solution/L-Xylose/pmc12845159-211-19-46
    Average 95 stars, based on 1 article reviews
    gus staining solution - by Bioz Stars, 2026-11
    95/100 stars

    Images

    1) Product Images from "Identification of a GA-Related Cis -Element Regulating Male Peduncle Elongation in Papaya"

    Article Title: Identification of a GA-Related Cis -Element Regulating Male Peduncle Elongation in Papaya

    Journal: Plants

    doi: 10.3390/plants15020209

    Histochemical staining of translational fusion constructs (designs in which a promoter drives the expression of a target gene coding sequence translationally fused to GUS, thereby producing a single fusion protein). Scale bars are 5 mm.
    Figure Legend Snippet: Histochemical staining of translational fusion constructs (designs in which a promoter drives the expression of a target gene coding sequence translationally fused to GUS, thereby producing a single fusion protein). Scale bars are 5 mm.

    Techniques Used: Staining, Construct, Expressing, Sequencing

    Related Articles

    other:

    Article Title: Membrane-associated effluxosomes coordinate multi-metal resistance in Mycobacterium tuberculosis.
    Article Snippet: Cultures were incubated for 3 h with 200 μM Biotin (Sigma, B4501) with shaking at 37 °C.

    Incubation:

    Article Title: Identification of a GA-Related Cis-Element Regulating Male Peduncle Elongation in Papaya
    Article Snippet: .. Various tissues from T3 transformants (leaf, inflorescence, stem, and pedicels) were collected 44 days after planting, and incubated in GUS staining solution (0.1 M NaPO4 at pH 7.0, 10 mM EDTA, 0.1% Triton X-100, 1 mM K3FE(CN)6 [Thermo Scientific], 2 mM X-Gluc [Gold Biotechnology, St. Louis, MO, USA]) overnight. ..

    Article Title: Membrane-associated effluxosomes coordinate multi-metal resistance in Mycobacterium tuberculosis
    Article Snippet: Lysis was performed by mechanical disruption 3 × 45 s (Biospec Minibeadbeater) with 5 min icing between runs. .. For biotinylated protein capture, protein lysates were mixed with 80 μL of Streptavidin-Agarose (GoldBio, S-105-10) prewashed 3X in 1 ml TBS and incubated rotating at 4 °C for 18 h. Agarose beads were collected at 250× g for 1 min at 4 °C and washed 2xs with 1 ml RIPA/SDS (TBS + 0.1% Triton X-100, 0.1% SDS, and 0.5% sodium deoxycholate) followed by four washes with TBS. .. Pooled supernatants were mixed with 150 μL of 10x RIPA buffer detergents (TBS + 10% Triton X-100, 1% SDS, and 5% sodium deoxycholate), mixed by inversion, and centrifuged at 20,000× g . The supernatant was filtered twice through EMD Millipore TM Ultrafree TM -CL Centrifugal Filter Devices with Durapore TM Membrane to remove any residual M. tuberculosis .

    Article Title: Motor learning and dopamine-dependent striatal synaptic plasticity are controlled by astrocytic MEGF10
    Article Snippet: After fixation, brains were obtained and postfixated overnight (4% PFA, 4 °C), followed by incubation in 30% sucrose (Sigma-Aldrich) in DPBS for at least 48 h. After, the brain was embedded in an OCT compound (Leica) and cryo-sectioned into 30 μm slices. .. Brain slices were incubated in blocking solution (4% bovine serum albumin, GoldBio; 0.3% Triton X-100, Sigma-Aldrich; in DPBS) for an hour at room temperature, followed by incubation in primary antibody solution (48 h, 4 °C). .. Primary antibodies were appropriately diluted in blocking solution (rabbit anti-S100β (1:500), Abcam #ab52642; guinea pig anti-S100β (1:500), Synaptic Systems #287004; rabbit anti-IBA1 (1:500), WAKO #019-19741; rabbit anti-tRFP (1:500), Evrogen #AB233; rat anti-mCherry (1:500), Invitrogen # M11217 ; chicken anti-GFP (1:2000), Aves Labs #GFP-1020; rabbit anti-c-Fos (1:500), Cell signaling technology #2250S; rabbit anti-HA (1:500), Cell signaling technology #3724; chicken anti-HA (1:500), Sigma-Aldrich #AB3254; sheep anti-TH (1:500), Sigma-Aldrich #AB1542; rabbit anti-TH (1:500), Sigma-Aldrich #AB152).

    Article Title: Identification of a GA-Related Cis -Element Regulating Male Peduncle Elongation in Papaya
    Article Snippet: .. Various tissues from T3 transformants (leaf, inflorescence, stem, and pedicels) were collected 44 days after planting, and incubated in GUS staining solution (0.1 M NaPO 4 at pH 7.0, 10 mM EDTA, 0.1% Triton X-100, 1 mM K 3 FE(CN) 6 [Thermo Scientific], 2 mM X-Gluc [Gold Biotechnology, St. Louis, MO, USA]) overnight. ..

    Article Title: ZINC-FINGER MOTIFS UNIQUE TO ARABIDOPSIS THALIANA PARALOGS RPA1C AND RPA1E ARE REQUIRED FOR RPA-DEPENDENT DNA REPAIR
    Article Snippet: .. Following fixation, plants were incubated in 50 mM NaPO 4 , pH 7.2, 0.5 mM K 3 Fe(CN) 6 , 0.5 mM K 4 Fe(CN) 6 , 10 mM EDTA, 0.01% Trition X-100, and 2 mM X-Gluc (Gold Biotechnology, St. Louis, MO, USA) overnight at 37°C. ..

    Staining:

    Article Title: Identification of a GA-Related Cis-Element Regulating Male Peduncle Elongation in Papaya
    Article Snippet: .. Various tissues from T3 transformants (leaf, inflorescence, stem, and pedicels) were collected 44 days after planting, and incubated in GUS staining solution (0.1 M NaPO4 at pH 7.0, 10 mM EDTA, 0.1% Triton X-100, 1 mM K3FE(CN)6 [Thermo Scientific], 2 mM X-Gluc [Gold Biotechnology, St. Louis, MO, USA]) overnight. ..

    Article Title: Identification of a GA-Related Cis -Element Regulating Male Peduncle Elongation in Papaya
    Article Snippet: .. Various tissues from T3 transformants (leaf, inflorescence, stem, and pedicels) were collected 44 days after planting, and incubated in GUS staining solution (0.1 M NaPO 4 at pH 7.0, 10 mM EDTA, 0.1% Triton X-100, 1 mM K 3 FE(CN) 6 [Thermo Scientific], 2 mM X-Gluc [Gold Biotechnology, St. Louis, MO, USA]) overnight. ..

    Blocking Assay:

    Article Title: Motor learning and dopamine-dependent striatal synaptic plasticity are controlled by astrocytic MEGF10
    Article Snippet: After fixation, brains were obtained and postfixated overnight (4% PFA, 4 °C), followed by incubation in 30% sucrose (Sigma-Aldrich) in DPBS for at least 48 h. After, the brain was embedded in an OCT compound (Leica) and cryo-sectioned into 30 μm slices. .. Brain slices were incubated in blocking solution (4% bovine serum albumin, GoldBio; 0.3% Triton X-100, Sigma-Aldrich; in DPBS) for an hour at room temperature, followed by incubation in primary antibody solution (48 h, 4 °C). .. Primary antibodies were appropriately diluted in blocking solution (rabbit anti-S100β (1:500), Abcam #ab52642; guinea pig anti-S100β (1:500), Synaptic Systems #287004; rabbit anti-IBA1 (1:500), WAKO #019-19741; rabbit anti-tRFP (1:500), Evrogen #AB233; rat anti-mCherry (1:500), Invitrogen # M11217 ; chicken anti-GFP (1:2000), Aves Labs #GFP-1020; rabbit anti-c-Fos (1:500), Cell signaling technology #2250S; rabbit anti-HA (1:500), Cell signaling technology #3724; chicken anti-HA (1:500), Sigma-Aldrich #AB3254; sheep anti-TH (1:500), Sigma-Aldrich #AB1542; rabbit anti-TH (1:500), Sigma-Aldrich #AB152).

    Luciferase:

    Article Title: Pathogen effector disarms circadian-immune crosstalk by targeting TCP14, a dual regulator of clock and defense.
    Article Snippet: .. Arabidopsis seedlings of luciferase reporter grown under 12 h light/12 h dark condition at 22◦C for 6 days were transferred to either constant light or diurnal condition and sprayed with 2.5 mM luciferin (Gold Biotechnology, LUCK-1G) in 0.02% Triton X-100 (Figures 1A, S1B, S3F, and S3G). ..

    Lysis:

    Article Title: The redundant protein synthesis gene Aimp1 challenges the canonical inverse relationship between translation and autophagy.
    Article Snippet: .. After 4 hours of exposure to Chlo or BafA1, HAP1 cells were lysed in lysis buffer containing 50 mM Tris-HCl (pH 7.6), 150 mM NaCl, 1.0% IGE-PAL, 0.5% Triton-X100, protease inhibitor cocktail (GoldBio, GB331-5), and Simple StopTM 1 Phosphatase Inhibitor Cocktail (GoldBio, GB-450-1). .. After 4 hours of exposure to Chlo or BafA1, HAP1 cells were lysed in lysis buffer containing 50 mM Tris-HCl (pH 7.6), 150 mM NaCl, 1.0% IGE-PAL, 0.5% Triton-X100, protease inhibitor cocktail (GoldBio, GB331-5), and Simple Stop 1 Phosphatase Inhibitor Cocktail (GoldBio, GB-450-1).

    Protease Inhibitor:

    Article Title: The redundant protein synthesis gene Aimp1 challenges the canonical inverse relationship between translation and autophagy.
    Article Snippet: .. After 4 hours of exposure to Chlo or BafA1, HAP1 cells were lysed in lysis buffer containing 50 mM Tris-HCl (pH 7.6), 150 mM NaCl, 1.0% IGE-PAL, 0.5% Triton-X100, protease inhibitor cocktail (GoldBio, GB331-5), and Simple StopTM 1 Phosphatase Inhibitor Cocktail (GoldBio, GB-450-1). .. After 4 hours of exposure to Chlo or BafA1, HAP1 cells were lysed in lysis buffer containing 50 mM Tris-HCl (pH 7.6), 150 mM NaCl, 1.0% IGE-PAL, 0.5% Triton-X100, protease inhibitor cocktail (GoldBio, GB331-5), and Simple Stop 1 Phosphatase Inhibitor Cocktail (GoldBio, GB-450-1).



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    SEM image of young spikes ( a ) and central florets ( b ) from Fielder <t>and</t> <t>AcRR1</t> -OE at the pistil and stamen formation stages. Scale bar, a 1 mm; b 0.5 mm. c Comparison of the florets number that eventually formed in Fielder and AcRR1 -OE. d <t>GUS</t> histochemical assays of Pro AcRR1 : GUS during young spike differentiation. I, floret differentiation stage; II, pistil and stamen formation stage; III, anther connective stage; IV, tetrad stage; V, white anther stage. Scale bar, 100 μm. In ( a ‒ d ) S, spikelet; F, floret primordia; AP, awn primordia; AF, apical floret; CF, central florets; BF, basal florets; A, anther. e , f Cytokinin and IAA contents of Fielder and AcRR1 -OE young spikes at the double ridge stage. g DEGs related to cytokinin degradation and biosynthesis in Fielder and AcRR1 -OE young spikes. h Expression of TaWOX11-2D in young spikes of AcRR1 -OE lines. i Direct binding of AcRR1 to the TaWOX11-2D promoter. j EMSA of the binding of AcRR1-His to the AGATN (A/T/C) motif in the TaWOX11-2D promoter. k ChIP‒qPCR assay of the binding of AcRR1 to the TaWOX11-2D promoter. l Representative spikes and middle spikelets of Jing 411 and the Tawox11-2D mutant. Scale bar, left, 2 cm; right, 1 cm. The grain number per spikelet ( m ) and grain number per spike ( n ) of F 2 TaWOX11-2D DD , TaWOX11-2D Dd and TaWOX11-2D dd plants derived from a cross of the Tawox11-2D mutant with Jing 411. o Direct binding of AcRR1 and wheat orthologs to the TaWOX11-2D promoter. The data are presented as the means ± S.D.s. In ( e ‒ i , k , o ) n = 3 biologically independent replicates. In ( c , m , n ) n represents the number of biologically independent plants. A two-tailed Student’s t test was used to determine P values. Source data are provided as a file.
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    SEM image of young spikes ( a ) and central florets ( b ) from Fielder <t>and</t> <t>AcRR1</t> -OE at the pistil and stamen formation stages. Scale bar, a 1 mm; b 0.5 mm. c Comparison of the florets number that eventually formed in Fielder and AcRR1 -OE. d <t>GUS</t> histochemical assays of Pro AcRR1 : GUS during young spike differentiation. I, floret differentiation stage; II, pistil and stamen formation stage; III, anther connective stage; IV, tetrad stage; V, white anther stage. Scale bar, 100 μm. In ( a ‒ d ) S, spikelet; F, floret primordia; AP, awn primordia; AF, apical floret; CF, central florets; BF, basal florets; A, anther. e , f Cytokinin and IAA contents of Fielder and AcRR1 -OE young spikes at the double ridge stage. g DEGs related to cytokinin degradation and biosynthesis in Fielder and AcRR1 -OE young spikes. h Expression of TaWOX11-2D in young spikes of AcRR1 -OE lines. i Direct binding of AcRR1 to the TaWOX11-2D promoter. j EMSA of the binding of AcRR1-His to the AGATN (A/T/C) motif in the TaWOX11-2D promoter. k ChIP‒qPCR assay of the binding of AcRR1 to the TaWOX11-2D promoter. l Representative spikes and middle spikelets of Jing 411 and the Tawox11-2D mutant. Scale bar, left, 2 cm; right, 1 cm. The grain number per spikelet ( m ) and grain number per spike ( n ) of F 2 TaWOX11-2D DD , TaWOX11-2D Dd and TaWOX11-2D dd plants derived from a cross of the Tawox11-2D mutant with Jing 411. o Direct binding of AcRR1 and wheat orthologs to the TaWOX11-2D promoter. The data are presented as the means ± S.D.s. In ( e ‒ i , k , o ) n = 3 biologically independent replicates. In ( c , m , n ) n represents the number of biologically independent plants. A two-tailed Student’s t test was used to determine P values. Source data are provided as a file.
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    SEM image of young spikes ( a ) and central florets ( b ) from Fielder <t>and</t> <t>AcRR1</t> -OE at the pistil and stamen formation stages. Scale bar, a 1 mm; b 0.5 mm. c Comparison of the florets number that eventually formed in Fielder and AcRR1 -OE. d <t>GUS</t> histochemical assays of Pro AcRR1 : GUS during young spike differentiation. I, floret differentiation stage; II, pistil and stamen formation stage; III, anther connective stage; IV, tetrad stage; V, white anther stage. Scale bar, 100 μm. In ( a ‒ d ) S, spikelet; F, floret primordia; AP, awn primordia; AF, apical floret; CF, central florets; BF, basal florets; A, anther. e , f Cytokinin and IAA contents of Fielder and AcRR1 -OE young spikes at the double ridge stage. g DEGs related to cytokinin degradation and biosynthesis in Fielder and AcRR1 -OE young spikes. h Expression of TaWOX11-2D in young spikes of AcRR1 -OE lines. i Direct binding of AcRR1 to the TaWOX11-2D promoter. j EMSA of the binding of AcRR1-His to the AGATN (A/T/C) motif in the TaWOX11-2D promoter. k ChIP‒qPCR assay of the binding of AcRR1 to the TaWOX11-2D promoter. l Representative spikes and middle spikelets of Jing 411 and the Tawox11-2D mutant. Scale bar, left, 2 cm; right, 1 cm. The grain number per spikelet ( m ) and grain number per spike ( n ) of F 2 TaWOX11-2D DD , TaWOX11-2D Dd and TaWOX11-2D dd plants derived from a cross of the Tawox11-2D mutant with Jing 411. o Direct binding of AcRR1 and wheat orthologs to the TaWOX11-2D promoter. The data are presented as the means ± S.D.s. In ( e ‒ i , k , o ) n = 3 biologically independent replicates. In ( c , m , n ) n represents the number of biologically independent plants. A two-tailed Student’s t test was used to determine P values. Source data are provided as a file.
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    Image Search Results


    Histochemical staining of translational fusion constructs (designs in which a promoter drives the expression of a target gene coding sequence translationally fused to GUS, thereby producing a single fusion protein). Scale bars are 5 mm.

    Journal: Plants

    Article Title: Identification of a GA-Related Cis -Element Regulating Male Peduncle Elongation in Papaya

    doi: 10.3390/plants15020209

    Figure Lengend Snippet: Histochemical staining of translational fusion constructs (designs in which a promoter drives the expression of a target gene coding sequence translationally fused to GUS, thereby producing a single fusion protein). Scale bars are 5 mm.

    Article Snippet: Various tissues from T3 transformants (leaf, inflorescence, stem, and pedicels) were collected 44 days after planting, and incubated in GUS staining solution (0.1 M NaPO 4 at pH 7.0, 10 mM EDTA, 0.1% Triton X-100, 1 mM K 3 FE(CN) 6 [Thermo Scientific], 2 mM X-Gluc [Gold Biotechnology, St. Louis, MO, USA]) overnight.

    Techniques: Staining, Construct, Expressing, Sequencing

    SEM image of young spikes ( a ) and central florets ( b ) from Fielder and AcRR1 -OE at the pistil and stamen formation stages. Scale bar, a 1 mm; b 0.5 mm. c Comparison of the florets number that eventually formed in Fielder and AcRR1 -OE. d GUS histochemical assays of Pro AcRR1 : GUS during young spike differentiation. I, floret differentiation stage; II, pistil and stamen formation stage; III, anther connective stage; IV, tetrad stage; V, white anther stage. Scale bar, 100 μm. In ( a ‒ d ) S, spikelet; F, floret primordia; AP, awn primordia; AF, apical floret; CF, central florets; BF, basal florets; A, anther. e , f Cytokinin and IAA contents of Fielder and AcRR1 -OE young spikes at the double ridge stage. g DEGs related to cytokinin degradation and biosynthesis in Fielder and AcRR1 -OE young spikes. h Expression of TaWOX11-2D in young spikes of AcRR1 -OE lines. i Direct binding of AcRR1 to the TaWOX11-2D promoter. j EMSA of the binding of AcRR1-His to the AGATN (A/T/C) motif in the TaWOX11-2D promoter. k ChIP‒qPCR assay of the binding of AcRR1 to the TaWOX11-2D promoter. l Representative spikes and middle spikelets of Jing 411 and the Tawox11-2D mutant. Scale bar, left, 2 cm; right, 1 cm. The grain number per spikelet ( m ) and grain number per spike ( n ) of F 2 TaWOX11-2D DD , TaWOX11-2D Dd and TaWOX11-2D dd plants derived from a cross of the Tawox11-2D mutant with Jing 411. o Direct binding of AcRR1 and wheat orthologs to the TaWOX11-2D promoter. The data are presented as the means ± S.D.s. In ( e ‒ i , k , o ) n = 3 biologically independent replicates. In ( c , m , n ) n represents the number of biologically independent plants. A two-tailed Student’s t test was used to determine P values. Source data are provided as a file.

    Journal: Nature Communications

    Article Title: AcRR1 of Agropyron cristatum boosts wheat yield by regulating grain number per spike and heading date

    doi: 10.1038/s41467-025-61917-5

    Figure Lengend Snippet: SEM image of young spikes ( a ) and central florets ( b ) from Fielder and AcRR1 -OE at the pistil and stamen formation stages. Scale bar, a 1 mm; b 0.5 mm. c Comparison of the florets number that eventually formed in Fielder and AcRR1 -OE. d GUS histochemical assays of Pro AcRR1 : GUS during young spike differentiation. I, floret differentiation stage; II, pistil and stamen formation stage; III, anther connective stage; IV, tetrad stage; V, white anther stage. Scale bar, 100 μm. In ( a ‒ d ) S, spikelet; F, floret primordia; AP, awn primordia; AF, apical floret; CF, central florets; BF, basal florets; A, anther. e , f Cytokinin and IAA contents of Fielder and AcRR1 -OE young spikes at the double ridge stage. g DEGs related to cytokinin degradation and biosynthesis in Fielder and AcRR1 -OE young spikes. h Expression of TaWOX11-2D in young spikes of AcRR1 -OE lines. i Direct binding of AcRR1 to the TaWOX11-2D promoter. j EMSA of the binding of AcRR1-His to the AGATN (A/T/C) motif in the TaWOX11-2D promoter. k ChIP‒qPCR assay of the binding of AcRR1 to the TaWOX11-2D promoter. l Representative spikes and middle spikelets of Jing 411 and the Tawox11-2D mutant. Scale bar, left, 2 cm; right, 1 cm. The grain number per spikelet ( m ) and grain number per spike ( n ) of F 2 TaWOX11-2D DD , TaWOX11-2D Dd and TaWOX11-2D dd plants derived from a cross of the Tawox11-2D mutant with Jing 411. o Direct binding of AcRR1 and wheat orthologs to the TaWOX11-2D promoter. The data are presented as the means ± S.D.s. In ( e ‒ i , k , o ) n = 3 biologically independent replicates. In ( c , m , n ) n represents the number of biologically independent plants. A two-tailed Student’s t test was used to determine P values. Source data are provided as a file.

    Article Snippet: Histochemical analysis of GUS activity in Pro AcRR1 : GUS transgenic lines was performed with a GUS staining solution (Solarbio, China) according to the manufacturer’s instructions.

    Techniques: Comparison, Expressing, Binding Assay, Mutagenesis, Derivative Assay, Two Tailed Test