Log In Sign up
The largest database of trusted experimental protocols

The A1106 is a laboratory centrifuge designed for general-purpose applications. It features a compact and durable construction, supporting a wide range of sample volumes and tube sizes. The centrifuge provides consistent and reliable performance to meet the needs of various laboratory workflows.

Automatically generated - may contain errors

Lab products found in correlation

A21428, by Thermo Fisher Scientific (4 mentions) Mab377, by Merck Group (4 mentions) Myelin basic protein, by Merck Group (4 mentions) Glial fibrillary acidic protein (gfap), by Merck Group (4 mentions) A11001, by Thermo Fisher Scientific (4 mentions) Neuronal nuclei (neun), by Merck Group (4 mentions)

4 protocols using a1106

1

Immunofluorescent Labeling of Apoptotic Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunofluorescence was also performed to identify apoptotic cells by co-labeling AC3 with antibodies that identify neurons (NeuN, EMD Millipore, Burlington, MA; MAB377, 1:100), astrocytes (GFAP, Sigma-Aldrich, St Louis, MO; G3893, 1:400), and oligodendrocytes (Myelin Basic Protein, EMD Millipore, Burlington, MA; MAB395, 1:200). Tissue was blocked and incubated in primary antibodies as described above. Finally, tissue was immersed in appropriate secondary antibodies (Invitrogen, Carlsbad, CA; A21428, A11001, or A1106) for one hour before cover-slipping with mounting medium containing DAPI.
Ikonomidou C., Wang S.H., Fuhler N.A., Larson S., Capuano S I.I.I., Brunner K.R., Crosno K., Simmons H.A., Mejia A.F, & Noguchi K.K. (2022). Mild hypothermia fails to protect infant macaques from brain injury caused by prolonged exposure to Antiseizure drugs. Neurobiology of disease, 171, 105814.
+ Open protocol
+ Expand
2

Immunofluorescent Labeling of Apoptotic Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunofluorescence was also performed to identify apoptotic cells by co-labeling AC3 with antibodies that identify neurons (NeuN, EMD Millipore, Burlington, MA; MAB377, 1:100), astrocytes (GFAP, Sigma-Aldrich, St Louis, MO; G3893, 1:400), and oligodendrocytes (Myelin Basic Protein, EMD Millipore, Burlington, MA; MAB395, 1:200). Tissue was blocked and incubated in primary antibodies as described above. Finally, tissue was immersed in appropriate secondary antibodies (Invitrogen, Carlsbad, CA; A21428, A11001, or A1106) for one hour before cover-slipping with mounting medium containing DAPI.
Noguchi K.K., Fuhler N.A., Wang S.H., Capuano S I.I.I., Brunner K.R., Larson S., Crosno K., Simmons H.A., Mejia A.F., Martin L.D., Dissen G.A., Brambrink A, & Ikonomidou C. (2020). Brain pathology caused in the neonatal macaque by short and prolonged exposures to anticonvulsant drugs. Neurobiology of disease, 149, 105245.
+ Open protocol
+ Expand
3

Immunofluorescent Labeling of Apoptotic Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunofluorescence was also performed to identify apoptotic cells by co-labeling AC3 with antibodies that identify neurons (NeuN, EMD Millipore, Burlington, MA; MAB377, 1:100), astrocytes (GFAP, Sigma-Aldrich, St Louis, MO; G3893, 1:400), and oligodendrocytes (Myelin Basic Protein, EMD Millipore, Burlington, MA; MAB395, 1:200). Tissue was blocked and incubated in primary antibodies as described above. Finally, tissue was immersed in appropriate secondary antibodies (Invitrogen, Carlsbad, CA; A21428, A11001, or A1106) for one hour before cover-slipping with mounting medium containing DAPI.
Noguchi K.K., Fuhler N.A., Wang S.H., Capuano S I.I.I., Brunner K.R., Larson S., Crosno K., Simmons H.A., Mejia A.F., Martin L.D., Dissen G.A., Brambrink A, & Ikonomidou C. (2020). Brain pathology caused in the neonatal macaque by short and prolonged exposures to anticonvulsant drugs. Neurobiology of disease, 149, 105245.
+ Open protocol
+ Expand
4

Immunofluorescent Labeling of Apoptotic Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunofluorescence was also performed to identify apoptotic cells by co-labeling AC3 with antibodies that identify neurons (NeuN, EMD Millipore, Burlington, MA; MAB377, 1:100), astrocytes (GFAP, Sigma-Aldrich, St Louis, MO; G3893, 1:400), and oligodendrocytes (Myelin Basic Protein, EMD Millipore, Burlington, MA; MAB395, 1:200). Tissue was blocked and incubated in primary antibodies as described above. Finally, tissue was immersed in appropriate secondary antibodies (Invitrogen, Carlsbad, CA; A21428, A11001, or A1106) for one hour before cover-slipping with mounting medium containing DAPI.
Ikonomidou C., Wang S.H., Fuhler N.A., Larson S., Capuano S I.I.I., Brunner K.R., Crosno K., Simmons H.A., Mejia A.F, & Noguchi K.K. (2022). Mild hypothermia fails to protect infant macaques from brain injury caused by prolonged exposure to Antiseizure drugs. Neurobiology of disease, 171, 105814.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!