rabbit polyclonal anticalbindin (cb) primary antibodies Search Results


93
Developmental Studies Hybridoma Bank mouse anti calbindin
Mouse Anti Calbindin, supplied by Developmental Studies Hybridoma Bank, 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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95
Cell Signaling Technology Inc rabbit anti calbindin antibody
Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation <t>calbindin</t> (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.
Rabbit Anti Calbindin Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Danaher Inc rabbit polyclonal anti calbindin
Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation <t>calbindin</t> (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.
Rabbit Polyclonal Anti Calbindin, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Danaher Inc rabbit polyclonal anticalbindin
Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation <t>calbindin</t> (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.
Rabbit Polyclonal Anticalbindin, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Swant rabbit anti-calbindin d-28 k
Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation <t>calbindin</t> (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.
Rabbit Anti Calbindin D 28 K, supplied by Swant, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Millipore rabbit anti-calbindin
Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation <t>calbindin</t> (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.
Rabbit Anti Calbindin, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Spring Bioscience rabbit anti-calbindin d28k e10340
Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation <t>calbindin</t> (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.
Rabbit Anti Calbindin D28k E10340, supplied by Spring Bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit anti-calbindin d28k e10340/product/Spring Bioscience
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90
Cell Signaling Technology Inc rabbit-anti-calbindin-d28k antibody
ERK activation in nonregenerative primary neuroretinal tissue. (A) Binimetinib reduced ERK activity (P-ERK) in primary neuroretinal tissue. MEK inhibition had no effect on the expression of <t>calbindin,</t> vinculin, and total ERK. (B) In all 7 neuroretinas, a reduction in ERK activity was observed after treatment with binimetinib. The differences in activity after treatment with binimetinib concentrations of 25 and 125 nM, when comparing to 0 nM, were significant ( P = 0.004 and P < 0.001, respectively). Between the binimetinib concentrations, no significant difference was seen in total ERK expression. The integrated intensities of both ERK and total ERK were corrected for vinculin ([{p}ERK/vinculin] × 100). Bars represent mean with SEM. ∗ P < 0.05 compared to control (0 nM), and ∗∗ P > 0.05 compared to control (0 nM). ERK = extracellular signal-regulated kinase, MEK = mitogen-activated protein kinase kinase, SEM = standard error of the mean.
Rabbit Anti Calbindin D28k Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit-anti-calbindin-d28k antibody/product/Cell Signaling Technology Inc
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99
OriGene mouse anti calbindin d 28k monoclonal antibody
KEY RESOURCES TABLE
Mouse Anti Calbindin D 28k Monoclonal Antibody, supplied by OriGene, 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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90
Millipore mouse or rabbit anti-calbindin-2
KEY RESOURCES TABLE
Mouse Or Rabbit Anti Calbindin 2, supplied by Millipore, 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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90
Merck KGaA rabbit anti-calbindin (hc)
Primary antibodies used for immunofluorescence.
Rabbit Anti Calbindin (Hc), supplied by Merck KGaA, 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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90
Millipore rabbit anti-gad65/67
Primary antibodies used for immunofluorescence.
Rabbit Anti Gad65/67, supplied by Millipore, 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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Image Search Results


Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation calbindin (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.

Journal: Cell reports

Article Title: Chronic Corticosterone Elevation Suppresses Adult Hippocampal Neurogenesis by Hyperphosphorylating Huntingtin.

doi: 10.1016/j.celrep.2020.107865

Figure Lengend Snippet: Figure 4. Phosphorylation of HTT at S1181/S1201 Influences Hippocampal Neurogenesis (A–C) Cells counts were performed in the DG of vehicle- and CORT-treated WT and HdhS1181A/S1201A mice (at least 4 for animals per condition) to quantify proliferation (Ki67+ cells, A), survival (BrdU+ cells, B), and immature neurons (DCX+ cells, C). *p < 0.05, **p < 0.01, ***p < 0.001. (D) Representative images show BrdU+ surviving cells (cyan) expressing (or not) the terminal marker for granule cell differentiation calbindin (magenta) on DG sections of WT and HdhS1181A/S1201A mice treated with vehicle or CORT. (E) The histogram shows the quantification of the number of BrdU+ and calbindin+ cells (3 animals per condition). *p <0.05, **p < 0.01. (F and G) Dendritic length (F) and complexity (G) were evaluated in both genotypes and treatment conditions (3 animals per condition). (H) Representative drawings of dendrites of DCX-positive neurons. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 comparing the HdhS1181A/S1201A vehicle group with the WT vehicle group, $p < 0.05, $$p < 0.01, $$$p < 0.001, $$$$p < 0.0001 comparing the HdhS1181A/S1201A -CORT group with the WT CORT group. Error bars, SEM. See also Figure S2.

Article Snippet: Slices were rinsed and blocked in 3% normal donkey serum in PBS containing 0.3% Triton X-100 for 1h at room temperature then incubated overnight at room temperature in 1:100 of mouse anti-BrdU antibody (#347580, BDBiosciences) and 1:500 rabbit anti-calbindin antibody (#13176, Cell Signaling Technologies).

Techniques: Phospho-proteomics, Expressing, Marker, Cell Differentiation

ERK activation in nonregenerative primary neuroretinal tissue. (A) Binimetinib reduced ERK activity (P-ERK) in primary neuroretinal tissue. MEK inhibition had no effect on the expression of calbindin, vinculin, and total ERK. (B) In all 7 neuroretinas, a reduction in ERK activity was observed after treatment with binimetinib. The differences in activity after treatment with binimetinib concentrations of 25 and 125 nM, when comparing to 0 nM, were significant ( P = 0.004 and P < 0.001, respectively). Between the binimetinib concentrations, no significant difference was seen in total ERK expression. The integrated intensities of both ERK and total ERK were corrected for vinculin ([{p}ERK/vinculin] × 100). Bars represent mean with SEM. ∗ P < 0.05 compared to control (0 nM), and ∗∗ P > 0.05 compared to control (0 nM). ERK = extracellular signal-regulated kinase, MEK = mitogen-activated protein kinase kinase, SEM = standard error of the mean.

Journal: Medicine

Article Title: Loss of MAPK Pathway Activation in Post-Mitotic Retinal Cells as Mechanism in MEK Inhibition-Related Retinopathy in Cancer Patients

doi: 10.1097/MD.0000000000003457

Figure Lengend Snippet: ERK activation in nonregenerative primary neuroretinal tissue. (A) Binimetinib reduced ERK activity (P-ERK) in primary neuroretinal tissue. MEK inhibition had no effect on the expression of calbindin, vinculin, and total ERK. (B) In all 7 neuroretinas, a reduction in ERK activity was observed after treatment with binimetinib. The differences in activity after treatment with binimetinib concentrations of 25 and 125 nM, when comparing to 0 nM, were significant ( P = 0.004 and P < 0.001, respectively). Between the binimetinib concentrations, no significant difference was seen in total ERK expression. The integrated intensities of both ERK and total ERK were corrected for vinculin ([{p}ERK/vinculin] × 100). Bars represent mean with SEM. ∗ P < 0.05 compared to control (0 nM), and ∗∗ P > 0.05 compared to control (0 nM). ERK = extracellular signal-regulated kinase, MEK = mitogen-activated protein kinase kinase, SEM = standard error of the mean.

Article Snippet: The primary antibodies used included mouse-anti-phospho-p44/42 ERK antibody (Sigma Aldrich), rabbit-anti-p44/42 ERK antibody (Cell Signalling Technologies, Danvers, MA), mouse-anti-vinculin antibody (Sigma Aldrich), and rabbit-anti-calbindin-D28K antibody (Cell Signalling Technologies).

Techniques: Activation Assay, Activity Assay, Inhibition, Expressing, Control

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: Overlapping Activities of Two Neuronal Splicing Factors Switch the GABA Effect from Excitatory to Inhibitory by Regulating REST

doi: 10.1016/j.celrep.2019.03.072

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: Mouse anti-calbindin D-28K monoclonal antibody (clone CB-955) , Acris Antibodies , Cat# AM08219SU-N; RRID: AB_1954252.

Techniques: Expressing, Plasmid Preparation, Recombinant, SYBR Green Assay, Reporter Assay, Isolation, Staining, Microarray, Clone Assay, Software

Primary antibodies used for immunofluorescence.

Journal: Frontiers in Neuroscience

Article Title: Dystrophin Is Required for the Proper Timing in Retinal Histogenesis: A Thorough Investigation on the mdx Mouse Model of Duchenne Muscular Dystrophy

doi: 10.3389/fnins.2020.00760

Figure Lengend Snippet: Primary antibodies used for immunofluorescence.

Article Snippet: Rabbit anti-calbindin (HC) , 1:1000 , Merck Millipore (Billerica, MA, United States).

Techniques: Immunofluorescence