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Vector Laboratories neurobiotin
( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
Neurobiotin, supplied by Vector Laboratories, 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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( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
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Vector Laboratories dylight
( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
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( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
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( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
Dylight 488 Streptavidin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Immuno alexa fluor 488
( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
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Vector Laboratories donkey anti fitc
( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
Donkey Anti Fitc, supplied by Vector Laboratories, 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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Jackson Immuno goat anti mouse igg alexa fluor 488
( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
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( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
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( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with <t>neurobiotin</t> (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.
Dylight 488, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vector Laboratories alexa fluor 488 goat antirat igg goat antirat igg
Antibody Table
Alexa Fluor 488 Goat Antirat Igg Goat Antirat Igg, supplied by Vector Laboratories, 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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Image Search Results


( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with neurobiotin (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.

Journal: bioRxiv

Article Title: Genetic tuning of intrinsically photosensitive retinal ganglion cell subtype identity to drive visual behavior

doi: 10.1101/2024.04.25.590656

Figure Lengend Snippet: ( A ) Representative dendritic arbor tracing of M4 and M2 ipRGCs in control and Brn3bcKO mice. ( B ) Subtype identified by presence (M4) or absence (M2) of SMI-32 immunolabeling (dashed ellipses), examples are from Brn3bcKO cells. ( C ) (Top) Scheme of retrogradely labeling strategy of M1 ipRGCs. (Bottom) Representative dendritic arbor tracing of M1 ipRGCs in control and Brn3bcKO mice. ( D ) Sholl analysis of M4, M2 and M1 ipRGC subtypes (n = 5-36 cells/group). ipRGCs from Brn3bcKO mice present less complex dendritic arbors compared to control mice. ( E - F ) Brn3bcKO showed decreased dendritic field diameter (E) (n = 5-36 cells/group) and soma size (F) (n = 19-36 cells/group) in M4, M2 and M1 ipRGC subtypes than control mice. ( G ) Representative picture of M4 ipRGCs (dashed ellipses) filled with neurobiotin (NB) used for electrophysiological recordings. ( H ) Brn3bcKO M4 ipRGCs showed increased input resistance compared to control M4 ipRGCs (n = 6-8/group). ( I ) M4 ipRGC subtype excitability in control and Brn3bcKO (n =5-7 cells/group) retinas. Brn3bcKO M4 ipRGCs reached peak firing rate by 300pA and then showed marked depolarization block ( J ) Representative traces of photocurrent of M4 ipRGCs from control (black) and Brn3bcKO retinas. ( K ) Maximum and sustained phases of photocurrent in M4 ipRGCs (n = 4-6 cells/group). All data are Mean ± SEM, n.s. (not significant) P>0.05, *P<0.05, ***P<0.001, Student’s t- and Mann Whitney U tests and two-way repeated measures ANOVA with Tukey’s multiple comparisons test.

Article Snippet: All recordings were made with internal solution containing 125 mM K-gluconate, 2 mM CaCl 2 , 2 mM MgCl 2 , 10 mM EGTA, 10 mM HEPES, 10 mM Na 2 -ATP, 0.5 mM Na-GTP, and 0.3% Neurobiotin (Vector Laboratories).

Techniques: Control, Immunolabeling, Labeling, Blocking Assay, MANN-WHITNEY

Antibody Table

Journal: Endocrinology

Article Title: Adiponectin Exerts Neurotrophic Effects on Dendritic Arborization, Spinogenesis, and Neurogenesis of the Dentate Gyrus of Male Mice

doi: 10.1210/en.2015-2078

Figure Lengend Snippet: Antibody Table

Article Snippet: Next day, the sections were coincubated with the following Alexa Fluor-conjugated secondary antibodies for 4 hours: antirabbit Alexa Fluor 647 goat IgG, antimouse Alexa Fluor 594 goat IgG, and antirat Alexa Fluor 488 goal IgG (1:400; Life Technologies) ( ). table ft1 table-wrap mode="anchored" t5 Table 1. caption a7 Peptide/Protein Target Antigen Sequence (if Known) Name of Antibody Manufacturer, Catalog Number, and/or Name of Individual Providing the Antibody Species Raised in; Monoclonal or Polyclonal Dilution Used Ki67 Synthetic peptide conjugated to KLH derived from within residues 1200 − 1300 of Human Ki67 Anti-Ki67 antibody Abcam, Ab15580 Rabbit; polyclonal 1:1000 Doublecortin (DCX) epitope mapping at the C-terminus of Doublecortin of human origin Doublecortin antibody (C-18) Santa Cruz Biotechnology, Inc, sc-8066 Goat; polyclonal 1:200 BrdU Anti-BrdU antibody [BU1/75 (ICR1)] Accurate Chemical, YSRTMCA2060GA Rat; monoclonal 1:400 NeuN Anti-NeuN antibody, clone A60 Millipore, MAB377 Mouse; monoclonal 1:1000 GFAP Anti-glial fibrillary acidic protein (GFAP) antibody Millipore, AB5804 Rabbit; polyclonal 1:1000 Biotinylated antirabbit IgG Biotinylated goat antirabbit IgG antibody Vector Laboratories, BA-1000 Goat 1:400 Biotinylated antigoat IgG Biotinylated horse antigoat IgG antibody Vector Laboratories, BA-9500 Horse 1:400 Alexa Fluor 488 goat antirat IgG Goat antirat IgG (H + L) secondary antibody, Alexa Fluor 488 conjugate Invitrogen, {"type":"entrez-nucleotide","attrs":{"text":"A11006","term_id":"492389","term_text":"A11006"}} A11006 Goat 1:400 Alexa Fluor 546 goat antimouse IgG F(ab')2-goat antimouse IgG (H + L) secondary antibody, Alexa Fluor 546 conjugate Invitrogen, {"type":"entrez-nucleotide","attrs":{"text":"A11018","term_id":"492393","term_text":"A11018"}} A11018 Goat 1:400 Alexa Fluor 647 goat antirabbit IgG F(ab')2-goat antirabbit IgG (H + L) secondary antibody, Alexa Fluor 647 conjugate Invitrogen, {"type":"entrez-nucleotide","attrs":{"text":"A21246","term_id":"641368","term_text":"A21246"}} A21246 Goat 1:400 Open in a separate window Abbreviation: H+L, Heavy and light chain.

Techniques: Sequencing, Derivative Assay, Plasmid Preparation