iba1 apc Search Results


neun iba1 apc aldh1  (Oxford Instruments)
99
Oxford Instruments neun iba1 apc aldh1
( A ) Representative xy maximally projected Z stacks (40 μm in depth) show <t>ALDH1</t> + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).
Neun Iba1 Apc Aldh1, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
neun iba1 apc aldh1 - by Bioz Stars, 2026-03
99/100 stars
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gr 1 a488  (R&D Systems)
92
R&D Systems gr 1 a488
( A ) Representative xy maximally projected Z stacks (40 μm in depth) show <t>ALDH1</t> + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).
Gr 1 A488, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
gr 1 a488 - by Bioz Stars, 2026-03
92/100 stars
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gr 1 a488  (Thermo Fisher)
86
Thermo Fisher gr 1 a488
( A ) Representative xy maximally projected Z stacks (40 μm in depth) show <t>ALDH1</t> + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).
Gr 1 A488, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
gr 1 a488 - by Bioz Stars, 2026-03
86/100 stars
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pe-anti-pser262-tau  (Thermo Fisher)
90
Thermo Fisher pe-anti-pser262-tau
( A ) Representative xy maximally projected Z stacks (40 μm in depth) show <t>ALDH1</t> + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).
Pe Anti Pser262 Tau, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90/100 stars
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anti iba 1 apc  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology anti iba 1 apc
( A ) Representative xy maximally projected Z stacks (40 μm in depth) show <t>ALDH1</t> + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).
Anti Iba 1 Apc, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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iba1 apc  (Bioss)
94
Bioss iba1 apc
( A ) Representative xy maximally projected Z stacks (40 μm in depth) show <t>ALDH1</t> + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).
Iba1 Apc, supplied by Bioss, 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/result/iba1 apc/product/Bioss
Average 94 stars, based on 1 article reviews
iba1 apc - by Bioz Stars, 2026-03
94/100 stars
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2e2 mouse santa cruz sc 293305 wb kv1 5 mouse alomone labs apc 004 wb iba1 rabbit wako  (Alomone Labs)
93
Alomone Labs 2e2 mouse santa cruz sc 293305 wb kv1 5 mouse alomone labs apc 004 wb iba1 rabbit wako
( A ) Representative xy maximally projected Z stacks (40 μm in depth) show <t>ALDH1</t> + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).
2e2 Mouse Santa Cruz Sc 293305 Wb Kv1 5 Mouse Alomone Labs Apc 004 Wb Iba1 Rabbit Wako, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
2e2 mouse santa cruz sc 293305 wb kv1 5 mouse alomone labs apc 004 wb iba1 rabbit wako - by Bioz Stars, 2026-03
93/100 stars
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aif1 iba1 polyclonal antibody, apc-cy5 conjugated  (Bioss)
N/A
Actin-binding protein that enhances membrane ruffling and RAC activation. Enhances the actin-bundling activity of LCP1. Binds calcium. Plays a role in RAC signaling and in phagocytosis. May play a role in macrophage activation and function.
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aif-1/iba1 antibody (031) [allophycocyanin]  (Novus Biologicals)
N/A
The AIF-1/Iba1 Antibody (031) [Allophycocyanin] from Novus is a AIF-1/Iba1 antibody to AIF-1/Iba1. This antibody reacts with Human. The AIF-1/Iba1 antibody has been validated for the following applications: ELISA, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry-Paraffin.
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aif-1/iba1 antibody (raif1/1909) [allophycocyanin]  (Novus Biologicals)
N/A
The AIF-1/Iba1 Antibody (rAIF1/1909) [Allophycocyanin] from Novus is a AIF-1/Iba1 antibody to AIF-1/Iba1. This antibody reacts with Human. The AIF-1/Iba1 antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin, Protein Array.
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aif1 iba1 polyclonal antibody, apc-cy5.5 conjugated  (Bioss)
N/A
Actin-binding protein that enhances membrane ruffling and RAC activation. Enhances the actin-bundling activity of LCP1. Binds calcium. Plays a role in RAC signaling and in phagocytosis. May play a role in macrophage activation and function.
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iba1 (aif-1) antibody, anti-human, apc, reafinity  (Miltenyi Biotec)
N/A
Detection of Iba1 (AIF1)+ cells
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Image Search Results


( A ) Representative xy maximally projected Z stacks (40 μm in depth) show ALDH1 + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).

Journal: JCI Insight

Article Title: Glia limitans superficialis oxidation and breakdown promote cortical cell death after repetitive head injury

doi: 10.1172/jci.insight.149229

Figure Lengend Snippet: ( A ) Representative xy maximally projected Z stacks (40 μm in depth) show ALDH1 + astrocytes (green) in Aldh1 CreER/+ Stop fl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. ( B ) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. ( C ) Quantification of SR101 leakage by mean fluorescent intensity (MFI). ( D ) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. ( E ) Quantification of cell death by selecting only PI + DAPI + cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with * P ≤ 0.05 and *** P ≤ 0.001 (2-tailed Student’s t test).

Article Snippet: To quantify individual cell types of interest (NeuN + , Iba1 + , APC + , ALDH1 + ), a 3-dimensional “spot” corresponding to each respective cell type was created in Imaris.

Techniques: Labeling