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catshark anti islet1 2 isl1 2 antibody  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank catshark anti islet1 2 isl1 2 antibody
    Catshark Anti Islet1 2 Isl1 2 Antibody, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 96/100, based on 278 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+islet1+antibody/anti-Islet-1+%26+Islet-2+homeobox/pm41699760-68-23-28
    Average 96 stars, based on 278 article reviews
    catshark anti islet1 2 isl1 2 antibody - by Bioz Stars, 2026-09
    96/100 stars

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    Staining:

    Article Title: Validation of human sensory neurons derived from inducible pluripotent stem cells as a model for latent infection and reactivation by herpes simplex virus 1
    Article Snippet: Primary antibodies were diluted in 5% (vol/vol) NGS diluted in 0.2 μm-filtered PBS and incubated overnight at 4°C.in 0.2 μm-filtered PBS and incubated overnight at 4°C. ... The primary antibodies used were anti-Nav1.7 antibody (Abcam, ab65167, 1:500 dilution), anti-Tuj1 antibody (Millipore, AB9354, 1:200 dilution), anti-peripherin antibody (Millipore, MAB1527, 1:500 dilution), anti-TRPV1 antibody (Alomone Labs, ACC-030, 1:200 dilution), anti-Brn3a antibody (Millipore, MAB1585, 1:500 dilution), anti-TrkB antibody (Protein Tech, 13129-1-AP, 1:25 dilution), anti-TrkC antibody (ThermoFisher, 7H3L20, 1:300 dilution), anti-Islet1 antibody (Developmental Studies Hybridoma Bank, 40.2D6, 1:50 dilution), anti-NeuN antibody (Millipore, MA377, 1:100 dilution), anti-Nav1.8 antibody (Alomone Labs, SCN10A, 1:100 dilution), anti-TRPA1 antibody (Alomone Labs, ACC-037, 1:50 dilution), anti-TRPM8 antibody (Alomone Labs, ACC-045, 1:100 dilution), and anti-SOX2 antibody (Abcam, ab97959, 1:200 dilution).. The day after, the unbound primary antibodies were washed away with filtered PBS three times.The day after, the unbound primary antibodies were washed..

    Article Title: Validation of human sensory neurons derived from inducible pluripotent stem cells as a model for latent infection and reactivation by herpes simplex virus 1.
    Article Snippet: Primary antibodies were diluted in 5% (vol/vol) NGS diluted in 0.2 μm-filtered PBS and incubated overnight at 4°C.. The primary antibodies used were anti-Nav1.7 antibody (Abcam, ab65167, 1:500 dilution), anti-Tuj1 antibody (Millipore, AB9354, 1:200 dilution), anti-peripherin antibody (Millipore, MAB1527, 1:500 dilution), anti-TRPV1 antibody (Alomone Labs, ACC-030, 1:200 dilution), anti-Brn3a antibody (Millipore, MAB1585, 1:500 dilution), anti-TrkB antibody (Protein Tech, 13129-1-AP, 1:25 dilution), anti-TrkC antibody (ThermoFisher, 7H3L20, 1:300 dilution), anti-Islet1 antibody (Developmental Studies Hybridoma Bank, 40.2D6, 1:50 dilution), anti-NeuN antibody (Millipore, MA377, 1:100 dilution), anti-Nav1.8 antibody (Alomone Labs, SCN10A, 1:100 dilution), anti-TRPA1 antibody (Alomone Labs, ACC-037, 1:50 dilution), anti-TRPM8 antibody (Alomone Labs, ACC-045, 1:100 dilution), and anti-SOX2 antibody (Abcam, Month XXXX Volume 0 Issue 0 10.1128/mbio.01871-2515 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/m bi o on 1 9 A ug us t 2 02 5 by 2 02 .5 1.. 69 .7 0. ab97959, 1:200 dilution).

    Article Title: Composition for prevention or treatment of spinocerebellar ataxia type 36
    Article Snippet: RNA foci in neurons or motor neurons were detected by treating the cells thus washed with 1×SSC, with a blocking buffer (buffer containing 5% bovine serum albumin and 0.2% Triton X-100) (room temperature, 20 minutes), followed by immunostaining.RNA foci in neurons or motor neurons were detected by treating the cells thus washed with 1×SSC, with a blocking buffer (buffer containing 5% bovine serum albumin and 0.2% Triton X-100) (room temperature, 20 minutes), followed by immunostaining.. The primary antibody used was an anti-β-III tubulin antibody (1:2,000; manufactured by Cell Signaling Technology, Inc.) or an anti-Islet1 antibody (1:200; manufactured by Developmental Studies Hybridoma Bank) (4° C., overnight), and the secondary antibody used was conjugated with Alexa (room temperature, 1 hour).. The immunostaining was performed using Fluor-conjugated.The immunostaining was performed using Fluor-conjugated.

    Article Title: Disabled-1 Alternative Splicing in Human Fetal Retina and Neural Tumors
    Article Snippet: Frozen sections were rehydrated in PBS, fixed in 4% PBS-buffered paraformaldehyde and permeabilized in 1% PBS-buffered NP-40.Frozen sections were rehydrated in PBS, fixed in 4% PBS-buffered paraformaldehyde and permeabilized in 1% PBS-buffered NP-40.. Sections were double-stained with rabbit polyclonal anti-Dab1 antibody prepared against the C-terminus of Dab1 (amino acids 400–555 which are common to both Dab1-E and Dab1-L-like isoforms) (1∶500) (Rockland Immunochemicals) and mouse anti-phospho-SFK Y416 antibody (clone 9A6) (1∶25) (Upstate), anti-Islet1 antibody (clone 39.4D5) (1∶500) (Developmental Studies Hybridoma Bank), anti-Ki67 antibody (clone MIB-1) (1∶1000) (Dakocytomation), or anti-AP2α antibody (clone 3B5) (1∶200) (Developmental Studies Hybridoma Bank).. The following secondary antibodies were used: Alexa 555-conjugated goat anti-rabbit for Dab1 and Alexa 488-conjugated donkey anti-mouse for SFK Y416 , Islet1, MIB-1 and AP2α (1∶150) (Invitrogen).The following secondary antibodies were used: Alexa 555-conjugated goat anti-rabbit for Dab1 and Alexa 488-conjugated donkey anti-mouse for SFK Y416 , Islet1, MIB-1 and AP2α (1∶150) (Invitrogen).

    Marker:

    Article Title: Validation of human sensory neurons derived from inducible pluripotent stem cells as a model for latent infection and reactivation by herpes simplex virus 1
    Article Snippet: Primary antibodies were diluted in 5% (vol/vol) NGS diluted in 0.2 μm-filtered PBS and incubated overnight at 4°C.in 0.2 μm-filtered PBS and incubated overnight at 4°C. ... The primary antibodies used were anti-Nav1.7 antibody (Abcam, ab65167, 1:500 dilution), anti-Tuj1 antibody (Millipore, AB9354, 1:200 dilution), anti-peripherin antibody (Millipore, MAB1527, 1:500 dilution), anti-TRPV1 antibody (Alomone Labs, ACC-030, 1:200 dilution), anti-Brn3a antibody (Millipore, MAB1585, 1:500 dilution), anti-TrkB antibody (Protein Tech, 13129-1-AP, 1:25 dilution), anti-TrkC antibody (ThermoFisher, 7H3L20, 1:300 dilution), anti-Islet1 antibody (Developmental Studies Hybridoma Bank, 40.2D6, 1:50 dilution), anti-NeuN antibody (Millipore, MA377, 1:100 dilution), anti-Nav1.8 antibody (Alomone Labs, SCN10A, 1:100 dilution), anti-TRPA1 antibody (Alomone Labs, ACC-037, 1:50 dilution), anti-TRPM8 antibody (Alomone Labs, ACC-045, 1:100 dilution), and anti-SOX2 antibody (Abcam, ab97959, 1:200 dilution).. The day after, the unbound primary antibodies were washed away with filtered PBS three times.The day after, the unbound primary antibodies were washed..

    Article Title: Validation of human sensory neurons derived from inducible pluripotent stem cells as a model for latent infection and reactivation by herpes simplex virus 1.
    Article Snippet: Primary antibodies were diluted in 5% (vol/vol) NGS diluted in 0.2 μm-filtered PBS and incubated overnight at 4°C.. The primary antibodies used were anti-Nav1.7 antibody (Abcam, ab65167, 1:500 dilution), anti-Tuj1 antibody (Millipore, AB9354, 1:200 dilution), anti-peripherin antibody (Millipore, MAB1527, 1:500 dilution), anti-TRPV1 antibody (Alomone Labs, ACC-030, 1:200 dilution), anti-Brn3a antibody (Millipore, MAB1585, 1:500 dilution), anti-TrkB antibody (Protein Tech, 13129-1-AP, 1:25 dilution), anti-TrkC antibody (ThermoFisher, 7H3L20, 1:300 dilution), anti-Islet1 antibody (Developmental Studies Hybridoma Bank, 40.2D6, 1:50 dilution), anti-NeuN antibody (Millipore, MA377, 1:100 dilution), anti-Nav1.8 antibody (Alomone Labs, SCN10A, 1:100 dilution), anti-TRPA1 antibody (Alomone Labs, ACC-037, 1:50 dilution), anti-TRPM8 antibody (Alomone Labs, ACC-045, 1:100 dilution), and anti-SOX2 antibody (Abcam, Month XXXX Volume 0 Issue 0 10.1128/mbio.01871-2515 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/m bi o on 1 9 A ug us t 2 02 5 by 2 02 .5 1.. 69 .7 0. ab97959, 1:200 dilution).

    Article Title: Composition for prevention or treatment of spinocerebellar ataxia type 36
    Article Snippet: RNA foci in neurons or motor neurons were detected by treating the cells thus washed with 1×SSC, with a blocking buffer (buffer containing 5% bovine serum albumin and 0.2% Triton X-100) (room temperature, 20 minutes), followed by immunostaining.RNA foci in neurons or motor neurons were detected by treating the cells thus washed with 1×SSC, with a blocking buffer (buffer containing 5% bovine serum albumin and 0.2% Triton X-100) (room temperature, 20 minutes), followed by immunostaining.. The primary antibody used was an anti-β-III tubulin antibody (1:2,000; manufactured by Cell Signaling Technology, Inc.) or an anti-Islet1 antibody (1:200; manufactured by Developmental Studies Hybridoma Bank) (4° C., overnight), and the secondary antibody used was conjugated with Alexa (room temperature, 1 hour).. The immunostaining was performed using Fluor-conjugated.The immunostaining was performed using Fluor-conjugated.

    Article Title: Disabled-1 Alternative Splicing in Human Fetal Retina and Neural Tumors
    Article Snippet: Frozen sections were rehydrated in PBS, fixed in 4% PBS-buffered paraformaldehyde and permeabilized in 1% PBS-buffered NP-40.Frozen sections were rehydrated in PBS, fixed in 4% PBS-buffered paraformaldehyde and permeabilized in 1% PBS-buffered NP-40.. Sections were double-stained with rabbit polyclonal anti-Dab1 antibody prepared against the C-terminus of Dab1 (amino acids 400–555 which are common to both Dab1-E and Dab1-L-like isoforms) (1∶500) (Rockland Immunochemicals) and mouse anti-phospho-SFK Y416 antibody (clone 9A6) (1∶25) (Upstate), anti-Islet1 antibody (clone 39.4D5) (1∶500) (Developmental Studies Hybridoma Bank), anti-Ki67 antibody (clone MIB-1) (1∶1000) (Dakocytomation), or anti-AP2α antibody (clone 3B5) (1∶200) (Developmental Studies Hybridoma Bank).. The following secondary antibodies were used: Alexa 555-conjugated goat anti-rabbit for Dab1 and Alexa 488-conjugated donkey anti-mouse for SFK Y416 , Islet1, MIB-1 and AP2α (1∶150) (Invitrogen).The following secondary antibodies were used: Alexa 555-conjugated goat anti-rabbit for Dab1 and Alexa 488-conjugated donkey anti-mouse for SFK Y416 , Islet1, MIB-1 and AP2α (1∶150) (Invitrogen).



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