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goat anti rat timp1  (R&D Systems)


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    R&D Systems goat anti rat timp1
    Fig. 1. Early-phase elevation of <t>TIMP-1</t> in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.
    Goat Anti Rat Timp1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/goat+anti+timp1/Rat+TIMP-1+Antibody/pm40158735-69-19-25
    Average 93 stars, based on 18 article reviews
    goat anti rat timp1 - by Bioz Stars, 2026-10
    93/100 stars

    Images

    1) Product Images from "TIMP-1 associates with myelin membrane and preserves myelin in injured peripheral nerve."

    Article Title: TIMP-1 associates with myelin membrane and preserves myelin in injured peripheral nerve.

    Journal: Neurobiology of disease

    doi: 10.1016/j.nbd.2025.106892

    Fig. 1. Early-phase elevation of TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.
    Figure Legend Snippet: Fig. 1. Early-phase elevation of TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.

    Techniques Used: Western Blot, Control

    Fig. 2. TIMP-1 in myelinating (m)SC and myelin sheath in CCI nerve. A, A myelinated axon (Ax) and mSC unit (a schematic). B, TIMP-1 immunofluores cence in rat sciatic nerve at days 0 (contralateral), 1, and 7 post-CCI; median (interquartile range) immunoreactivity count per (81,380 μm2 endoneurial area) of n = 6–7/group (3–4 male, 3–4 female), 3 sections/n; Kruskal-Wallis test with Dunn-Bonferoni post-hoc were used for p = value Red circle, female; blue square, male. C, MBP (green) and TIMP-1 (red) dual-IF shows TIMP-1 in MBP- reactive mSC cytoplasm (arrowheads) and myelin sheaths (arrows) in CCI nerves; DAPI (blue). Scale bar, 10 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
    Figure Legend Snippet: Fig. 2. TIMP-1 in myelinating (m)SC and myelin sheath in CCI nerve. A, A myelinated axon (Ax) and mSC unit (a schematic). B, TIMP-1 immunofluores cence in rat sciatic nerve at days 0 (contralateral), 1, and 7 post-CCI; median (interquartile range) immunoreactivity count per (81,380 μm2 endoneurial area) of n = 6–7/group (3–4 male, 3–4 female), 3 sections/n; Kruskal-Wallis test with Dunn-Bonferoni post-hoc were used for p = value Red circle, female; blue square, male. C, MBP (green) and TIMP-1 (red) dual-IF shows TIMP-1 in MBP- reactive mSC cytoplasm (arrowheads) and myelin sheaths (arrows) in CCI nerves; DAPI (blue). Scale bar, 10 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Techniques Used:

    Fig. 3. Myelin/membrane (mm)TIMP-1 in fractionated CCI nerve. A, FLOT-1 (47 kD, lipid raft marker) and MBP (14, 18 kD, myelin marker) immunoblot ting in rat sciatic nerve sucrose fractions (1−12) at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group, female shown. FLOT-1 and MBP in light/buoyant fractions (4,5,6), defined as myelin/membrane lipid rafts. FLOT-1 in heavy/ non-buoyant fractions (10,11,12). B, TIMP-1 (28 kD) immunoblotting of frac tions (4,5,6) in rat sciatic nerve at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group. TL, total lysate control; M, molecular weight standard. C, LC- MS/MS analysis of rat female sciatic nerve sample [4–6] at day 1 post-CCI, as in A-B, concentrated using an Ultracel-10 membrane filter. Note TIMP-1 (rat, Accession #P30120) and myelin proteins, P0 (rat, MYP0, Accession #P06907) and MBP (rat, Accession #P02688), in the myelin/membrane lipid raft fraction.
    Figure Legend Snippet: Fig. 3. Myelin/membrane (mm)TIMP-1 in fractionated CCI nerve. A, FLOT-1 (47 kD, lipid raft marker) and MBP (14, 18 kD, myelin marker) immunoblot ting in rat sciatic nerve sucrose fractions (1−12) at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group, female shown. FLOT-1 and MBP in light/buoyant fractions (4,5,6), defined as myelin/membrane lipid rafts. FLOT-1 in heavy/ non-buoyant fractions (10,11,12). B, TIMP-1 (28 kD) immunoblotting of frac tions (4,5,6) in rat sciatic nerve at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group. TL, total lysate control; M, molecular weight standard. C, LC- MS/MS analysis of rat female sciatic nerve sample [4–6] at day 1 post-CCI, as in A-B, concentrated using an Ultracel-10 membrane filter. Note TIMP-1 (rat, Accession #P30120) and myelin proteins, P0 (rat, MYP0, Accession #P06907) and MBP (rat, Accession #P02688), in the myelin/membrane lipid raft fraction.

    Techniques Used: Membrane, Marker, Western Blot, Control, Molecular Weight, Liquid Chromatography with Mass Spectroscopy

    Fig. 4. Time-course of (mm)TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in fractionated rat sciatic nerve in samples [4–6] and [10–12] at days 0 (contralateral) and 1 post-CCI. FLOT-1 (47 kD) as lipid rafts marker/loading control. Exposure times: 1-12 min. B, The mean TIMP-1 to FLOT-1 ratio in sample [4–6] at days 0, 1, 7, and 28 post-CCI ± SEM of n = 6–8/group (2–4 male, 3–5 female); by one-way ANOVA and Student’s t-test. -Representative of A.
    Figure Legend Snippet: Fig. 4. Time-course of (mm)TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in fractionated rat sciatic nerve in samples [4–6] and [10–12] at days 0 (contralateral) and 1 post-CCI. FLOT-1 (47 kD) as lipid rafts marker/loading control. Exposure times: 1-12 min. B, The mean TIMP-1 to FLOT-1 ratio in sample [4–6] at days 0, 1, 7, and 28 post-CCI ± SEM of n = 6–8/group (2–4 male, 3–5 female); by one-way ANOVA and Student’s t-test. -Representative of A.

    Techniques Used: Western Blot, Marker, Control

    Related Articles

    other:

    Article Title: Single cell RNA sequencing analysis of mouse cochlear supporting cell transcriptomes with activated ERBB2 receptor indicates a cell-specific response that promotes CD44 activation
    Article Snippet: The following primary antibodies were used: chicken anti-GFP (1:100; Abcam; AB_300798), mouse anti-PVALB (1:1,000, EMD Millipore; MAB1572), goat anti-OPN (SPP1; 1:100; R&D Systems; AF808), goat anti-TIMP1 (1:100; R&D Systems; AF980), rabbit anti-CD44 (1:100; Abcam; AB157107), rabbit anti-pERBB2 (1:200; Santa Cruz; sc-12352), goat anti-SOX2 (1:500; Santa Cruz; sc-17320), rabbit anti-MYO7 (1:1,000; Proteus; 25-6790), rabbit anti-activated CASP3 (1:500; R&D Systems, AF835), and rabbit anti-TAK1 (1:500; Thermo Fisher Scientific; 28H25L68).

    Article Title: Single cell RNA sequencing analysis of mouse cochlear supporting cell transcriptomes with activated ERBB2 receptor, a candidate mediator of hearing restoration mechanisms.
    Article Snippet: The following primary antibodies were used: chicken anti-GFP (1:100; Abcam; AB_300798), mouse anti-PVALB (1:1000, EMD Millipore; MAB1572), goat anti-OPN (1:100; R&D Systems; AF808), goat anti-TIMP1 (1:100; R&D Systems; AF980), rabbit anti-CD44 (1:100; Abcam; AB157107).

    Article Title: Role of macrophages in regression of myocardial fibrosis following alleviation of left ventricular pressure overload.
    Article Snippet: Sustained hemodynamic pressure overload (PO) produced by murine transverse aortic constriction (TAC) causes myocardial fibrosis; removal of TAC (unTAC) returns left ventricle (LV) hemodynamic load to normal and results in significant, but incomplete regression of myocardial fibrosis.. However, the cellular mechanisms that result in these outcomes have not been defined.. The objective was to determine temporal changes in myocardial macrophage phenotype in TAC and unTAC and determine whether macrophage depletion alters collagen degradation after unTAC.

    Article Title: Single cell RNA sequencing analysis of mouse cochlear supporting cell transcriptomes with activated ERBB2 receptor, a candidate mediator of hearing restoration mechanisms
    Article Snippet: The following primary antibodies were used: chicken anti-GFP (1:100; Abcam; AB_300798), mouse anti-PVALB (1:1000, EMD Millipore; MAB1572), goat anti-OPN (1:100; R&D Systems; AF808), goat anti-TIMP1 (1:100; R&D Systems; AF980), rabbit anti-CD44 (1:100; Abcam; AB157107).

    Article Title: Single cell RNA sequencing analysis of mouse cochlear supporting cell transcriptomes with activated ERBB2 receptor indicates a cell-specific response that promotes CD44 activation.
    Article Snippet: The following primary antibodies were used: chicken anti-GFP (1:100; Abcam; AB_300798), mouse anti-PVALB (1:1,000, EMD Millipore; MAB1572), goat antiOPN (SPP1; 1:100; R&D Systems; AF808), goat anti-TIMP1 (1:100; R&D Systems; AF980), rabbit anti-CD44 (1:100; Abcam; AB157107), rabbit anti-pERBB2 (1:200; Santa Cruz; sc-12352), goat anti-SOX2 (1:500; Santa Cruz; sc-17320), rabbit antiMYO7 (1:1,000; Proteus; 25-6790), rabbit anti-activated CASP3 (1:500; R&D Systems, AF835), and rabbit anti-TAK1 (1:500; Thermo Fisher Scientific; 28H25L68).



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    Fig. 1. Early-phase elevation of <t>TIMP-1</t> in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.
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    Fig. 1. Early-phase elevation of <t>TIMP-1</t> in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.
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    Fig. 1. Early-phase elevation of <t>TIMP-1</t> in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.
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    Image Search Results


    Fig. 1. Early-phase elevation of TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.

    Journal: Neurobiology of disease

    Article Title: TIMP-1 associates with myelin membrane and preserves myelin in injured peripheral nerve.

    doi: 10.1016/j.nbd.2025.106892

    Figure Lengend Snippet: Fig. 1. Early-phase elevation of TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in rat sciatic nerve total lysates at days 0 (contralateral), 1, 7, and 28 post- CCI, using GAPDH (36 kD) as a loading control. B, The mean TIMP-1 to GAPDH ratio ± SEM of n = 6 (3 male, 3 female) rats/group of A.; by one-way ANOVA with Tukey’s post-hoc test, or Student’s t-test. C, The mean TIMP-1 to GAPDH ratio ± SEM of n = 3 male vs. 3 female rats/group of B.; by one-way ANOVA with Tukey’s post-hoc test. B-C: n.s, not significant.

    Article Snippet: Nonspecific binding was blocked with 10 % normal donkey serum (Sigma, 1 h, room temperature) and incubated overnight with goat anti-rat Timp1 (1:50; Cat# AF580, R&D Systems) and rabbit anti-MBP (1:100; Cat# ab40390, Abcam) primary antibodies (4 ◦C, 16–18 h).

    Techniques: Western Blot, Control

    Fig. 2. TIMP-1 in myelinating (m)SC and myelin sheath in CCI nerve. A, A myelinated axon (Ax) and mSC unit (a schematic). B, TIMP-1 immunofluores cence in rat sciatic nerve at days 0 (contralateral), 1, and 7 post-CCI; median (interquartile range) immunoreactivity count per (81,380 μm2 endoneurial area) of n = 6–7/group (3–4 male, 3–4 female), 3 sections/n; Kruskal-Wallis test with Dunn-Bonferoni post-hoc were used for p = value Red circle, female; blue square, male. C, MBP (green) and TIMP-1 (red) dual-IF shows TIMP-1 in MBP- reactive mSC cytoplasm (arrowheads) and myelin sheaths (arrows) in CCI nerves; DAPI (blue). Scale bar, 10 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Journal: Neurobiology of disease

    Article Title: TIMP-1 associates with myelin membrane and preserves myelin in injured peripheral nerve.

    doi: 10.1016/j.nbd.2025.106892

    Figure Lengend Snippet: Fig. 2. TIMP-1 in myelinating (m)SC and myelin sheath in CCI nerve. A, A myelinated axon (Ax) and mSC unit (a schematic). B, TIMP-1 immunofluores cence in rat sciatic nerve at days 0 (contralateral), 1, and 7 post-CCI; median (interquartile range) immunoreactivity count per (81,380 μm2 endoneurial area) of n = 6–7/group (3–4 male, 3–4 female), 3 sections/n; Kruskal-Wallis test with Dunn-Bonferoni post-hoc were used for p = value Red circle, female; blue square, male. C, MBP (green) and TIMP-1 (red) dual-IF shows TIMP-1 in MBP- reactive mSC cytoplasm (arrowheads) and myelin sheaths (arrows) in CCI nerves; DAPI (blue). Scale bar, 10 μm. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Article Snippet: Nonspecific binding was blocked with 10 % normal donkey serum (Sigma, 1 h, room temperature) and incubated overnight with goat anti-rat Timp1 (1:50; Cat# AF580, R&D Systems) and rabbit anti-MBP (1:100; Cat# ab40390, Abcam) primary antibodies (4 ◦C, 16–18 h).

    Techniques:

    Fig. 3. Myelin/membrane (mm)TIMP-1 in fractionated CCI nerve. A, FLOT-1 (47 kD, lipid raft marker) and MBP (14, 18 kD, myelin marker) immunoblot ting in rat sciatic nerve sucrose fractions (1−12) at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group, female shown. FLOT-1 and MBP in light/buoyant fractions (4,5,6), defined as myelin/membrane lipid rafts. FLOT-1 in heavy/ non-buoyant fractions (10,11,12). B, TIMP-1 (28 kD) immunoblotting of frac tions (4,5,6) in rat sciatic nerve at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group. TL, total lysate control; M, molecular weight standard. C, LC- MS/MS analysis of rat female sciatic nerve sample [4–6] at day 1 post-CCI, as in A-B, concentrated using an Ultracel-10 membrane filter. Note TIMP-1 (rat, Accession #P30120) and myelin proteins, P0 (rat, MYP0, Accession #P06907) and MBP (rat, Accession #P02688), in the myelin/membrane lipid raft fraction.

    Journal: Neurobiology of disease

    Article Title: TIMP-1 associates with myelin membrane and preserves myelin in injured peripheral nerve.

    doi: 10.1016/j.nbd.2025.106892

    Figure Lengend Snippet: Fig. 3. Myelin/membrane (mm)TIMP-1 in fractionated CCI nerve. A, FLOT-1 (47 kD, lipid raft marker) and MBP (14, 18 kD, myelin marker) immunoblot ting in rat sciatic nerve sucrose fractions (1−12) at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group, female shown. FLOT-1 and MBP in light/buoyant fractions (4,5,6), defined as myelin/membrane lipid rafts. FLOT-1 in heavy/ non-buoyant fractions (10,11,12). B, TIMP-1 (28 kD) immunoblotting of frac tions (4,5,6) in rat sciatic nerve at day 1 post-CCI. Rep. of n = 6 (3 male, 3 female) per group. TL, total lysate control; M, molecular weight standard. C, LC- MS/MS analysis of rat female sciatic nerve sample [4–6] at day 1 post-CCI, as in A-B, concentrated using an Ultracel-10 membrane filter. Note TIMP-1 (rat, Accession #P30120) and myelin proteins, P0 (rat, MYP0, Accession #P06907) and MBP (rat, Accession #P02688), in the myelin/membrane lipid raft fraction.

    Article Snippet: Nonspecific binding was blocked with 10 % normal donkey serum (Sigma, 1 h, room temperature) and incubated overnight with goat anti-rat Timp1 (1:50; Cat# AF580, R&D Systems) and rabbit anti-MBP (1:100; Cat# ab40390, Abcam) primary antibodies (4 ◦C, 16–18 h).

    Techniques: Membrane, Marker, Western Blot, Control, Molecular Weight, Liquid Chromatography with Mass Spectroscopy

    Fig. 4. Time-course of (mm)TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in fractionated rat sciatic nerve in samples [4–6] and [10–12] at days 0 (contralateral) and 1 post-CCI. FLOT-1 (47 kD) as lipid rafts marker/loading control. Exposure times: 1-12 min. B, The mean TIMP-1 to FLOT-1 ratio in sample [4–6] at days 0, 1, 7, and 28 post-CCI ± SEM of n = 6–8/group (2–4 male, 3–5 female); by one-way ANOVA and Student’s t-test. -Representative of A.

    Journal: Neurobiology of disease

    Article Title: TIMP-1 associates with myelin membrane and preserves myelin in injured peripheral nerve.

    doi: 10.1016/j.nbd.2025.106892

    Figure Lengend Snippet: Fig. 4. Time-course of (mm)TIMP-1 in CCI nerve. A, TIMP-1 (28 kD) immunoblotting in fractionated rat sciatic nerve in samples [4–6] and [10–12] at days 0 (contralateral) and 1 post-CCI. FLOT-1 (47 kD) as lipid rafts marker/loading control. Exposure times: 1-12 min. B, The mean TIMP-1 to FLOT-1 ratio in sample [4–6] at days 0, 1, 7, and 28 post-CCI ± SEM of n = 6–8/group (2–4 male, 3–5 female); by one-way ANOVA and Student’s t-test. -Representative of A.

    Article Snippet: Nonspecific binding was blocked with 10 % normal donkey serum (Sigma, 1 h, room temperature) and incubated overnight with goat anti-rat Timp1 (1:50; Cat# AF580, R&D Systems) and rabbit anti-MBP (1:100; Cat# ab40390, Abcam) primary antibodies (4 ◦C, 16–18 h).

    Techniques: Western Blot, Marker, Control