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Proteintech iba1
Iba1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 390 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/iba1/IBA1+Polyclonal+antibody/10__1038_slash_s42003___026___10891___9-300-45-47
Average 96 stars, based on 390 article reviews
iba1 - by Bioz Stars, 2026-10
96/100 stars

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Related Articles

Incubation:

Article Title: Dual-responsive PDA-HP hydrogel enables mitochondria-targeted mild photothermal therapy for spinal cord repair
Article Snippet: .. Samples were then incubated overnight at 4 °C with the following primary antibodies: GFAP (astrocyte marker, 1:500, Proteintech, China), Iba1 (microglia marker, 1:500, Proteintech, China), Arg-1 (M2 phenotype marker, 1:500, Proteintech, China), iNOS (M1 phenotype marker, 1:500, Proteintech, China). .. After rinsing, sections were incubated with Alexa Fluor 488- or 594-conjugated secondary antibodies (1:1000, Proteintech, China) for 1 h at room temperature in the dark, followed by counterstaining with DAPI (1 μg/mL, 8 min).

Article Title: Modulating GRP75 to restore calcium homeostasis: a novel neuroprotective strategy of CRSE6 # in Parkinson's disease models.
Article Snippet: .. Next, sections were incubated in 0.5% Triton X100 for 30 min at room temperature and then closed in 5% BSA for 1 h. The primary antibody was added and incubated at 4 °C overnight, IBA1 (Proteintech, 10904-1-A P), GFAP (Proteintech, 60190- 1-Ig), a-syn (Affinity, AF6258), GRP75 Polyclonal antibody (14887-1-AP, Proteintech, 14887-1-AP), VDAC1 Monoclonal antibody (Proteintech, 66345-1-AP), and IP3R-I (Santz Cruz, sc271197.) and BAX Monoclonal antibody (Proteintech, 60267-1- Ig), Bcl-2 Antibody (Affinity, AF6139). .. Sections were rinsed with PBS and incubated with fluorescently labeled secondary antibodies (Cat# RGAM002, RGAR004, RGAR002, Proteintech, Wuhan, China) for 1 h, followed by restaining with DAPI for 10 min.

Article Title: Mechanism of Qufeng Huoxue decoction in treating paclitaxel-induced peripheral neuropathy based on network pharmacology and molecular docking.
Article Snippet: Background and purpose: Chemotherapy-induced peripheral neuropathy (CIPN) is a common adverse reaction in cancer patients, affecting 30–50% of patients' quality of life.. Qufeng Huoxue Decoction (QHD), has been used for many years as an adjunctive treatment for CIPN in China.. However, the underlying mechanism of the role of Qufeng Huoxue Decoction in PIPN remains elusive.

Marker:

Article Title: Dual-responsive PDA-HP hydrogel enables mitochondria-targeted mild photothermal therapy for spinal cord repair
Article Snippet: .. Samples were then incubated overnight at 4 °C with the following primary antibodies: GFAP (astrocyte marker, 1:500, Proteintech, China), Iba1 (microglia marker, 1:500, Proteintech, China), Arg-1 (M2 phenotype marker, 1:500, Proteintech, China), iNOS (M1 phenotype marker, 1:500, Proteintech, China). .. After rinsing, sections were incubated with Alexa Fluor 488- or 594-conjugated secondary antibodies (1:1000, Proteintech, China) for 1 h at room temperature in the dark, followed by counterstaining with DAPI (1 μg/mL, 8 min).

Cell-Signaling:

Article Title: Microglial METTL14 mediated m⁶A regulation of ATG13 promotes autophagy and functional recovery after spinal cord injury
Article Snippet: .. The following primary antibodies were used: TNFα (1: 500, Abcam, EPR19147), METTL14 (1: 500 Proteintech, 26158-1-AP), GFAP(1: 1000, Cell Signaling Technology, 3670), LC3B(1: 600, Cell Signaling Technology, 83506), NeuN(1: 300, Abcam, ab177487), inos(1: 600, abcam, ab178945), TMEM119(1: 600, ab209064, Abcam), Beclin(1: 500, Abcam, ab62557) and Iba1(1: 200, Proteintech, 10904-1-AP). .. After thorough washing with PBS, the sections were incubated with fluorescently labeled secondary antibodies (Alexa Fluor 488, 594, and 647, Abcam) for 2 h at room temperature.

other:

Article Title: Targeting the HDAC4-NHE6-endosomal pH axis restores amyloid-β clearance and cognitive function in Alzheimer's disease mice.
Article Snippet: 108 2 Materials and Methods 109 Materials 110 The antibodies used are as follows: IBA1 (Oasis, OB-PGP049-01), Aβ (BioLegend, 111 800708), LRP1 (ZRB1311), GFAP (FujiFilm, MO389), β-amyloid-FITC (MCE, HY112 P3908), LAMP2 (Proteintech, 66301-1-Ig), S100A10 (Proteintech, 11250-1-AP).



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Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn <t>(green)/Iba1</t> (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).
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Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn <t>(green)/Iba1</t> (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).
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Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn <t>(green)/Iba1</t> (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).
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Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn <t>(green)/Iba1</t> (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).
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Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn <t>(green)/Iba1</t> (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).
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Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn <t>(green)/Iba1</t> (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).
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Image Search Results


Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn (green)/Iba1 (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).

Journal: PLOS One

Article Title: AZP2006 in Parkinson’s disease models: A promising new neuroprotective treatment involving lysosomal homeostasis and the Progranulin/Prosaposin complex

doi: 10.1371/journal.pone.0359269

Figure Lengend Snippet: Body mass evolution during 35 days of daily treatment with vehicle or AZP2006 post-lesion (A). Representative IHC images TH (red)/α-syn (green)/Iba1 (purple) (B). IHC analysis shows the total number of TH(+) neurons (C), area of α-syn accumulation in TH(+) neurons (D) and the number of Iba1(+) microglia in the SNpc (E) expressed as % of sham. Raw values for sham (i.e., 100%); TH(+) neurons = 65 ± 1.6; α-syn area/TH(+) neuron = 168 ± 9.4 µm 2 ; Iba1(+) cells = 53 ± 2.8. Each bar represents the mean ± SEM, one-way ANOVA followed by Fisher’s test. ## p < 0.01 or #### p < 0.0001 from sham; **p < 0.01; ***p < 0.001 and ****p < 0.0001 from α-syn+vehicle injury, (n = 7 mice / group).

Article Snippet: Iba1 , Rabbit , Polyclonal , Novus , NBP2–19019 , AB_3073939 , .

Techniques: Analysis

Antibodies used for in vivo investigations.

Journal: PLOS One

Article Title: AZP2006 in Parkinson’s disease models: A promising new neuroprotective treatment involving lysosomal homeostasis and the Progranulin/Prosaposin complex

doi: 10.1371/journal.pone.0359269

Figure Lengend Snippet: Antibodies used for in vivo investigations.

Article Snippet: Iba1 , Rabbit , Polyclonal , Novus , NBP2–19019 , AB_3073939 , .

Techniques: In Vivo, Cell-Signaling