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Structured Review

Proteintech anti map2
Anti Map2, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 465 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+map2/MAP2+Antibody/10__1038_slash_s41467___026___77831___3-628-5-7
Average 96 stars, based on 465 article reviews
anti map2 - by Bioz Stars, 2026-10
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Images

Related Articles

Immunostaining:

Article Title: TP53/TAU axis regulates microtubule bundling to control alveolar stem cell–mediated regeneration
Article Snippet: Images were recorded using a 20× objective of the Axio imager (ZEISS). .. The following antibodies and dyes were applied to samples for immunostaining: anti-RAGE/AGER (MAB1179, R&D Systems, 1:500), anti-proSP-C (AB3786, MilliporeSigma, 1:500), anti-ABCA3 (3C9) (sc58220, Santa Cruz Biotechnology, 1:300), anti-Claudin4 (36-4800, Invitrogen, 1:200), anti-Actin, alpha-Smooth Muscle Cy3-conjugated (C6198, MilliporeSigma,1:500), anti-HT1-56 (TB-29AHT1-56, Terrace Biotech, 1:300), anti-HTII-280 (TB-27AHT2-280, Terrace Biotech, 1:50), anti-GFP (NB100-1770, Novus Biologicals, 1:500), anti-tdTomato (AB8181-200, OriGene, 1:1,000), anti-TUBA1A antibody (PA5-22060, Invitrogen, 1:100), anti-TUBA1B (66031-1-Ig, Proteintech, 1:500), anti-acetylated Tubulin (66200-1-Ig, Proteintech, 1:500), anti-Tau (10274-1-AP, Proteintech, 1:200), anti-Tau-1 (PC1C6) (MAB3420, MilliporeSigma,1:100), anti-Tau (Tau-5) (AHB0042, Invitrogen,1:50), anti-MAP2 (17490-1-AP, Proteintech, 1:500), anti-Keratin8 (TROMA-I, DSHB, 1:50), anti-GM130 (610822, BD Biosciences, 1:50), Alexa Fluor-555 Phalloidin (A34055, Invitrogen, 1:400), Alexa Fluor-647 Phalloidin (A22287, Invitrogen, 1:400), LEL-DyLight-649 (DL-1178, Vector Laboratories,1:1,500), anti-FLAG-M2 (F1804, Sigma-Aldrich, 1;1,000), anti-Calnexin (AB22595, Abcam, 1:500), anti-CD107a/LAMP-1 (121601, BioLegend, 1:500), anti-SFN (PA5-95056, Invitrogen, 1:250), anti-LGALS3-Alexa647 (125408, BioLegend, 1:500), and anti-TAGLN/Transgelin (ab14106, Abcam, 1:250). .. Images were captured using an Olympus FV3000 confocal microscope with 20×, 30×, 40×, and 60× objectives.

Article Title: TP53/TAU axis regulates microtubule bundling to control alveolar stem cell mediated regeneration
Article Snippet: Images were recorded using a 20X objective of 709 Axio imager (Zeiss). .. 710 711 Antibodies 712 The following antibodies and dyes were applied to samples for immunostaining: anti-713 RAGE/AGER (MAB1179, R&D systems, 1:500), anti-proSP-C (AB3786, MilliporeSigma, 1:500), 714 anti-ABCA3 (3C9) (sc58220, Santacruz, 1:300), anti-Claudin4 (36-4800, Invitrogen, 1:200), anti-715 Actin, alpha-Smooth Muscle Cy3-conjugated (C6198, MilliporeSigma,1:500), anti-HT1-56 (TB-716 29AHT1-56, Terrace Biotech, 1:300), anti-HTII-280 (TB-27AHT2-280, Terrace Biotech, 1:50), 717 anti-GFP (NB100-1770, Novus Biologicals, 1:500), anti-tdTomato (AB8181-200, Origene, 718 1:1000), anti-TUBA1A antibody (PA5-22060, Invitrogen, 1:100), anti-TUBA1B (66031-1-Ig, 719 Proteintech, 1:500), anti-acetylated Tubulin (66200-1-Ig, Proteintech, 1:500), anti-Tau (10274-1-720 AP, Proteintech, 1:200), anti-Tau-1 (PC1C6) (MAB3420, MilliporeSigma,1:100), anti-Tau (Tau-5) 721 (AHB0042, Invitrogen,1:50), anti-MAP2 (17490-1-AP, Proteintech, 1:500), anti-Keratin8 722 (TROMA-I, DSHB, 1:50), anti-GM130 (610822, BD, 1:50), Alexa Fluor-555 Phalloidin (A34055, 723 Invitrogen,, 1:400), Alexa Fluor-647 Phalloidin (A22287, Invitrogen,, 1:400), LEL-DyLight-649 724 (DL-1178, Vector Laboratories,1:1500), anti-FLAG-M2 (F1804, Sigma-Aldrich, 1;1000), anti-725 Calnexin (AB22595, Abcam, 1:500), anti-CD107a/LAMP-1 (121601, BioLegend, 1:500), anti-SFN 726 (PA5-95056, Invitrogen, 1:250), anti-LGALS3-Alexa647 (125408, BioLegend, 1:500), anti-727 TAGLN/Transgelin (ab14106, Abcam, 1:250). .. 728 729 Image acquisition, processing and quantification 730 Images were captured using an Olympus FV3000 confocal microscope with a 20X, 30X, 40X, 731 60X objectives.

Incubation:

Article Title: MAP2-mediated integrin dysregulation reprograms cancer cell plasticity in hepatocellular carcinoma
Article Snippet: .. 1μg lysate was incubated with anti-MAP2 (5μg, Proteintech, 17490-1-AP), anti-Actin (5μg, Proteintech, 66009-1-IG), mouse IgG (5μg, eBioscience, 14-4714-82) or rabbit IgG antibodies (5μg, Bethyl Laboratories, P120-101) with gentle shaking overnight at 4 °C. .. The lysate was then incubated with Protein A Sepharose beads (for antiMAP2 and rabbit IgG, Abcam, ab193256) or Protein G agarose beads (for anti-Actin and mouse IgG, Roche, 10060954) with gentle shaking for 4 h at 4 °C.

Article Title: ISX9 activates the Wnt/β-catenin signaling pathway and exerts neuroprotective effects in Alzheimer’s disease
Article Snippet: .. Following blocking, cells were incubated with anti-β-catenin (Proteintech, Cat#51667-2-AP), anti-LGR5 (Affinity Biotech, Cat#DF2816), anti-NeuN (Proteintech, Cat#26975-1-AP), anti-NeuroD1 (Proteintech, Cat#12081-1-AP) and anti-MAP2 (Proteintech, Cat17490-1-AP) antibodies at 4 °C overnight. .. Alexa Fluor 594 conjugated goat anti-mouse IgG antibodies (Thermo Fisher Scientific, Cat#A11032) were used as secondary antibodies.

Gentle:

Article Title: MAP2-mediated integrin dysregulation reprograms cancer cell plasticity in hepatocellular carcinoma
Article Snippet: .. 1μg lysate was incubated with anti-MAP2 (5μg, Proteintech, 17490-1-AP), anti-Actin (5μg, Proteintech, 66009-1-IG), mouse IgG (5μg, eBioscience, 14-4714-82) or rabbit IgG antibodies (5μg, Bethyl Laboratories, P120-101) with gentle shaking overnight at 4 °C. .. The lysate was then incubated with Protein A Sepharose beads (for antiMAP2 and rabbit IgG, Abcam, ab193256) or Protein G agarose beads (for anti-Actin and mouse IgG, Roche, 10060954) with gentle shaking for 4 h at 4 °C.

Blocking Assay:

Article Title: ISX9 activates the Wnt/β-catenin signaling pathway and exerts neuroprotective effects in Alzheimer’s disease
Article Snippet: .. Following blocking, cells were incubated with anti-β-catenin (Proteintech, Cat#51667-2-AP), anti-LGR5 (Affinity Biotech, Cat#DF2816), anti-NeuN (Proteintech, Cat#26975-1-AP), anti-NeuroD1 (Proteintech, Cat#12081-1-AP) and anti-MAP2 (Proteintech, Cat17490-1-AP) antibodies at 4 °C overnight. .. Alexa Fluor 594 conjugated goat anti-mouse IgG antibodies (Thermo Fisher Scientific, Cat#A11032) were used as secondary antibodies.



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Syb2‐containing neuronal EV uptake in the somatodendritic compartment depends on Dynamin and occurs independently of macropinocytosis. (A) Experimental design. (B) Representative confocal images of neuronal cell bodies labeled with Dex (yellow), immunofluorescently labeled with <t>anti‐MAP2</t> (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (C, D) Number of Dex and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (C) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 50.83, p < 0.0001. (D) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 27.15, p < 0.0001. (E) Experimental design. (F) Representative confocal images of neuronal cell bodies labeled with Tf (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (G, H) Number of Tf and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (G) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 49.51, p < 0.0001. (H) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 29.31, p < 0.0001. For C, D and G, H: data are shown as box and whisker plots with each dot representing one individual neuron; results from Dunn's multiple comparisons test are displayed on the figure; data from 3 independent cultures.
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Syb2‐containing neuronal EV uptake in the somatodendritic compartment depends on Dynamin and occurs independently of macropinocytosis. (A) Experimental design. (B) Representative confocal images of neuronal cell bodies labeled with Dex (yellow), immunofluorescently labeled with <t>anti‐MAP2</t> (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (C, D) Number of Dex and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (C) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 50.83, p < 0.0001. (D) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 27.15, p < 0.0001. (E) Experimental design. (F) Representative confocal images of neuronal cell bodies labeled with Tf (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (G, H) Number of Tf and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (G) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 49.51, p < 0.0001. (H) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 29.31, p < 0.0001. For C, D and G, H: data are shown as box and whisker plots with each dot representing one individual neuron; results from Dunn's multiple comparisons test are displayed on the figure; data from 3 independent cultures.
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Waveform rescue and impairment of AIS in C9-MSNs (A) Example AP waveforms for Con-1 (blue) and C9-3 MSNs (black) before and after the addition of BK channel activator NS11021 (10 μM, lighter color shade). Scale bars, 20 mV, 10 ms. (B and C) Mean ± SEM AP amplitude, AHP, half-width, threshold, and rheobase of C9-3 MSNs in the presence and absence of NS11021, along with Con-1 MSNs, were examined in parallel. Statistics, ∗ p < 0.05 and ∗∗∗ p < 0.001, from paired t test or t test . Data: con-1: n = 8, N = 3. C9-3: n = 10, N = 4. (D) NS11021 treatment had no effect on AP output in C9-3 MSNs evoked from current stimulation. Con-1 patched in parallel, shown for reference. Data: Con-1: n = 8, N = 3. C9-3: n = 10, N = 4. Statistics, two-way repeated measures ANOVA followed by Tukey’s multiple comparisons test. (E) Images of Con-1 and C9-3 stained with AIS marker ankyrin-G, neuronal marker <t>MAP2,</t> and DAPI. Scale bars, 50 μm. (F) Mean ± SEM AIS length and distance of start of AIS from the cell soma. Data: Con-1: n = 16, N = 4. C9-3: n = 36, N = 4. ∗∗∗ p < 0.001, t test.
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Image Search Results


Syb2‐containing neuronal EV uptake in the somatodendritic compartment depends on Dynamin and occurs independently of macropinocytosis. (A) Experimental design. (B) Representative confocal images of neuronal cell bodies labeled with Dex (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (C, D) Number of Dex and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (C) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 50.83, p < 0.0001. (D) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 27.15, p < 0.0001. (E) Experimental design. (F) Representative confocal images of neuronal cell bodies labeled with Tf (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (G, H) Number of Tf and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (G) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 49.51, p < 0.0001. (H) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 29.31, p < 0.0001. For C, D and G, H: data are shown as box and whisker plots with each dot representing one individual neuron; results from Dunn's multiple comparisons test are displayed on the figure; data from 3 independent cultures.

Journal: Journal of Neurochemistry

Article Title: Synaptobrevin‐2 Containing Extracellular Vesicles Are Rapidly Incorporated Into Mammalian Neurons via a Dynamin‐Dependent Pathway

doi: 10.1111/jnc.70551

Figure Lengend Snippet: Syb2‐containing neuronal EV uptake in the somatodendritic compartment depends on Dynamin and occurs independently of macropinocytosis. (A) Experimental design. (B) Representative confocal images of neuronal cell bodies labeled with Dex (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (C, D) Number of Dex and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (C) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 50.83, p < 0.0001. (D) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 27.15, p < 0.0001. (E) Experimental design. (F) Representative confocal images of neuronal cell bodies labeled with Tf (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 20 μm. (G, H) Number of Tf and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (G) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 49.51, p < 0.0001. (H) Kruskal – Wallis non‐parametric test, Kruskal–Wallis statistic = 29.31, p < 0.0001. For C, D and G, H: data are shown as box and whisker plots with each dot representing one individual neuron; results from Dunn's multiple comparisons test are displayed on the figure; data from 3 independent cultures.

Article Snippet: After blocking with 3% BSA, primary antibodies against GFP (1:150) (Invitrogen, Cat. No. A11122, RRID:AB_221569), Syn1 (1:500) (Synaptic Systems, Cat. No. 106011, RRID:AB_10805139), Syp1 (1:500) (Synaptic Systems, Cat. No. 101006, RRID: AB_2622239), and/or MAP2 (1:1000) (Synaptic Systems, Cat. No. 188004, RRID:AB_2138181) were diluted in blocking buffer and incubated overnight at 4°C in a humid chamber.

Techniques: Labeling, Negative Control, Whisker Assay

Syb2‐containing neuronal EV uptake in the axonal compartment is Dynamin‐dependent and occurs independently of macropinocytosis. (A) Experimental design. (B) Representative confocal images of synapses labeled with Dex (yellow), immunofluorescently labeled with anti‐Syp1 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 5 μm. (C, D) Number of Dex and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (C) Kruskal‐Wallis non‐parametric test, Kruskal–Wallis statistic = 48.26, p < 0.0001. (D) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 46.09, p < 0.0001. (E) Experimental design. (F) Representative confocal images of neuronal cell bodies labeled with Tf (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 5 μm. (G, H) Number of Tf and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (G) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 35.22, p < 0.0001. (D) Kruskal‐Wallis non‐parametric test, Kruskal–Wallis statistic = 30.51, p < 0.0001. For C, D and G, H: data are shown as box and whisker plots and each dot is the average of all presynaptic boutons quantified in one image; results from Dunn's multiple comparisons test are displayed on the figure; data from 3 independent cultures.

Journal: Journal of Neurochemistry

Article Title: Synaptobrevin‐2 Containing Extracellular Vesicles Are Rapidly Incorporated Into Mammalian Neurons via a Dynamin‐Dependent Pathway

doi: 10.1111/jnc.70551

Figure Lengend Snippet: Syb2‐containing neuronal EV uptake in the axonal compartment is Dynamin‐dependent and occurs independently of macropinocytosis. (A) Experimental design. (B) Representative confocal images of synapses labeled with Dex (yellow), immunofluorescently labeled with anti‐Syp1 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 5 μm. (C, D) Number of Dex and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (C) Kruskal‐Wallis non‐parametric test, Kruskal–Wallis statistic = 48.26, p < 0.0001. (D) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 46.09, p < 0.0001. (E) Experimental design. (F) Representative confocal images of neuronal cell bodies labeled with Tf (yellow), immunofluorescently labeled with anti‐MAP2 (magenta) and anti‐GFP (cyan). Z‐stacks of images are shown, presented as the maximum intensity projection of the volumetric data. White scale bars = 5 μm. (G, H) Number of Tf and GFP (EV‐delivered Syb2‐pHluorin) clusters in negative control, DMSO‐treated, and EIPA‐treated groups. (G) Kruskal–Wallis non‐parametric test, Kruskal–Wallis statistic = 35.22, p < 0.0001. (D) Kruskal‐Wallis non‐parametric test, Kruskal–Wallis statistic = 30.51, p < 0.0001. For C, D and G, H: data are shown as box and whisker plots and each dot is the average of all presynaptic boutons quantified in one image; results from Dunn's multiple comparisons test are displayed on the figure; data from 3 independent cultures.

Article Snippet: After blocking with 3% BSA, primary antibodies against GFP (1:150) (Invitrogen, Cat. No. A11122, RRID:AB_221569), Syn1 (1:500) (Synaptic Systems, Cat. No. 106011, RRID:AB_10805139), Syp1 (1:500) (Synaptic Systems, Cat. No. 101006, RRID: AB_2622239), and/or MAP2 (1:1000) (Synaptic Systems, Cat. No. 188004, RRID:AB_2138181) were diluted in blocking buffer and incubated overnight at 4°C in a humid chamber.

Techniques: Labeling, Negative Control, Whisker Assay

Journal: Cell reports

Article Title: Pleiotrophin regulates presynaptic assembly and function through heparan sulfate-dependent binding to neurexin1

doi: 10.1016/j.celrep.2026.117827

Figure Lengend Snippet:

Article Snippet: Chicken anti-MAP2 , Synaptic Systems , Cat# 188006; RRID:AB_2619881.

Techniques: Virus, Recombinant, Magnetic Beads, Mass Spectrometry, shRNA, Sequencing, Software

Waveform rescue and impairment of AIS in C9-MSNs (A) Example AP waveforms for Con-1 (blue) and C9-3 MSNs (black) before and after the addition of BK channel activator NS11021 (10 μM, lighter color shade). Scale bars, 20 mV, 10 ms. (B and C) Mean ± SEM AP amplitude, AHP, half-width, threshold, and rheobase of C9-3 MSNs in the presence and absence of NS11021, along with Con-1 MSNs, were examined in parallel. Statistics, ∗ p < 0.05 and ∗∗∗ p < 0.001, from paired t test or t test . Data: con-1: n = 8, N = 3. C9-3: n = 10, N = 4. (D) NS11021 treatment had no effect on AP output in C9-3 MSNs evoked from current stimulation. Con-1 patched in parallel, shown for reference. Data: Con-1: n = 8, N = 3. C9-3: n = 10, N = 4. Statistics, two-way repeated measures ANOVA followed by Tukey’s multiple comparisons test. (E) Images of Con-1 and C9-3 stained with AIS marker ankyrin-G, neuronal marker MAP2, and DAPI. Scale bars, 50 μm. (F) Mean ± SEM AIS length and distance of start of AIS from the cell soma. Data: Con-1: n = 16, N = 4. C9-3: n = 36, N = 4. ∗∗∗ p < 0.001, t test.

Journal: Cell Reports

Article Title: Striatal neuron dysfunction in C9ORF72-FTD/ALS is driven by AIS and potassium channel dysregulation

doi: 10.1016/j.celrep.2026.117672

Figure Lengend Snippet: Waveform rescue and impairment of AIS in C9-MSNs (A) Example AP waveforms for Con-1 (blue) and C9-3 MSNs (black) before and after the addition of BK channel activator NS11021 (10 μM, lighter color shade). Scale bars, 20 mV, 10 ms. (B and C) Mean ± SEM AP amplitude, AHP, half-width, threshold, and rheobase of C9-3 MSNs in the presence and absence of NS11021, along with Con-1 MSNs, were examined in parallel. Statistics, ∗ p < 0.05 and ∗∗∗ p < 0.001, from paired t test or t test . Data: con-1: n = 8, N = 3. C9-3: n = 10, N = 4. (D) NS11021 treatment had no effect on AP output in C9-3 MSNs evoked from current stimulation. Con-1 patched in parallel, shown for reference. Data: Con-1: n = 8, N = 3. C9-3: n = 10, N = 4. Statistics, two-way repeated measures ANOVA followed by Tukey’s multiple comparisons test. (E) Images of Con-1 and C9-3 stained with AIS marker ankyrin-G, neuronal marker MAP2, and DAPI. Scale bars, 50 μm. (F) Mean ± SEM AIS length and distance of start of AIS from the cell soma. Data: Con-1: n = 16, N = 4. C9-3: n = 36, N = 4. ∗∗∗ p < 0.001, t test.

Article Snippet: MAP2 anti-Rabbit (1:1000) , Synaptic Systems , Cat# 188 003; RRID AB_2281442.

Techniques: Staining, Marker