human m1 achr (Alomone Labs)


Structured Review

Human M1 Achr, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human m1 achr/product/Alomone Labs
Average 92 stars, based on 1 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque"
Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque
Journal: Brain and Behavior
doi: 10.1002/brb3.225

Figure Legend Snippet: Qualitative detail of single-label immunoperoxidase reactivity for m1 ACh receptors, panels A and B) and parvalbumin (C and D) in visual areas V1 (A and C) and the middle temporal visual area (MT) (B and D). The micrograph in panel A shows m1 AChR-immunoreactivity in layer 5 of area V1. Panel B shows m1 AChR-immunoreactivity in layer 3 of MT. In both panels the characteristic stained cytoplasmic ring around an immunonegative nuclear region is evident (asterisks). When immunoreactive dendrites are evident, they are usually (arrowhead in A), but not always (arrowhead in B) visibly attached to a cell body. There was no axonal staining evident in either cortical area. Parvalbumin immunoreactivity (C and D) on the other hand, is evident in cell bodies, dendrites (arrowheads in C and D) and axons (arrows in D). Panel C is a micrograph captured in layer 2 of area V1. The parvalbumin immunoreactivity shown in Panel D is of layer 5 in MT. Scale bar = 20 μ m.
Techniques Used: Staining

Figure Legend Snippet: Most m1 AChR-immunoreactive neurons (panel B, magenta) in the middle temporal visual area (MT) are not immunoreactive for parvalbumin (PV; panel A, green). This image was captured in layer 5 of area MT using a 40× objective. There are seven PV neurons in the imaged field (+, A). Note that the cell body marked with a ∼ in panel A would not have been counted in this study as it does not have a clearly defined boundary within the imaging plane, although it is a PV neuron. Five of these seven PV neurons are also immunoreactive for the m1 AChR (+ in B and C). Two are m1-immunonegative (arrows in B). A striking feature of this image is the number of neurons that are immunoreactive for m1 AChRs (B, C), but not PV (A). Although these singly labeled m1-ir neurons occasionally appear pyramidal (*), it is generally not possible to determine cell morphology (or, therefore, cell class) from the immunoreactivity for m1 AChRs. The strongly fluorescent regions circled in B and C would not have been counted as they do not appear somatic in shape. These regions appear in only one channel and can thus be distinguished from the lipofuscin autofluorescence (∧ in A, B, and C) which is equally strong but appears in all channels. Scale bar = 100 μ m.
Techniques Used: Imaging, Labeling

Figure Legend Snippet: Quantification of m1 AChR expression by parvalbumin neurons. The graphs show the percentage of parvalbumin (PV) neurons encountered, by cortical layer, that were also immunoreactive for m1 AChRs in areas V1 (A) and the middle temporal visual area (MT) (B). Error bars represent SEM. Number of PV neurons in each graph is the same: V1 = 293 PV neurons, MT = 293 PV neurons.
Techniques Used: Expressing

Figure Legend Snippet: Quantification of the parvalbumin-immunoreactive population as a percentage of m1 AChR-expressing neurons. The graphs show the percentage of m1 AChR-expressing neurons encountered, by cortical layer, that were also immunoreactive for parvalbumin in areas V1 (A) and the middle temporal visual area (MT) (B). Error bars represent SEM. Number of m1 AChR-ir neurons: V1 = 520, MT = 1081.
Techniques Used: Expressing

Figure Legend Snippet: The distributions of soma sizes are similar between the populations of singly and dually labeled neurons in V1 (A) or the middle temporal visual area (MT) (B). In these histograms of soma sizes, measured along the long axis, it can be seen that in V1 (A) the distributions for singly-labeled parvalbumin (PV)- and m1 AChR-ir neurons, and for dually immunoreactive neurons are unimodal and centered around 12–14 microns. In MT these distributions are shifted to the right and somewhat skewed, with a long tail at the end representing soma sizes greater than 20 μ m. This tail of the distribution has a very small N , but all three groups (single PV-ir, single m1AChR-ir and dual PV/m1-ir) are represented in the population of neurons with large somata, offering no evidence for a bi-modal distribution of soma size in either cortical area. N for V1: m1 single = 52, PV single = 11, dual = 50 neurons. N for MT: m1 single = 52, PV single = 12, dual = 45 neurons.
Techniques Used: Labeling
human m1 achr (Alomone Labs)


Structured Review

Human M1 Achr, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human m1 achr/product/Alomone Labs
Average 92 stars, based on 1 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque"
Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque
Journal: Brain and Behavior
doi: 10.1002/brb3.225

Figure Legend Snippet: Qualitative detail of single-label immunoperoxidase reactivity for m1 ACh receptors, panels A and B) and parvalbumin (C and D) in visual areas V1 (A and C) and the middle temporal visual area (MT) (B and D). The micrograph in panel A shows m1 AChR-immunoreactivity in layer 5 of area V1. Panel B shows m1 AChR-immunoreactivity in layer 3 of MT. In both panels the characteristic stained cytoplasmic ring around an immunonegative nuclear region is evident (asterisks). When immunoreactive dendrites are evident, they are usually (arrowhead in A), but not always (arrowhead in B) visibly attached to a cell body. There was no axonal staining evident in either cortical area. Parvalbumin immunoreactivity (C and D) on the other hand, is evident in cell bodies, dendrites (arrowheads in C and D) and axons (arrows in D). Panel C is a micrograph captured in layer 2 of area V1. The parvalbumin immunoreactivity shown in Panel D is of layer 5 in MT. Scale bar = 20 μ m.
Techniques Used: Staining

Figure Legend Snippet: Most m1 AChR-immunoreactive neurons (panel B, magenta) in the middle temporal visual area (MT) are not immunoreactive for parvalbumin (PV; panel A, green). This image was captured in layer 5 of area MT using a 40× objective. There are seven PV neurons in the imaged field (+, A). Note that the cell body marked with a ∼ in panel A would not have been counted in this study as it does not have a clearly defined boundary within the imaging plane, although it is a PV neuron. Five of these seven PV neurons are also immunoreactive for the m1 AChR (+ in B and C). Two are m1-immunonegative (arrows in B). A striking feature of this image is the number of neurons that are immunoreactive for m1 AChRs (B, C), but not PV (A). Although these singly labeled m1-ir neurons occasionally appear pyramidal (*), it is generally not possible to determine cell morphology (or, therefore, cell class) from the immunoreactivity for m1 AChRs. The strongly fluorescent regions circled in B and C would not have been counted as they do not appear somatic in shape. These regions appear in only one channel and can thus be distinguished from the lipofuscin autofluorescence (∧ in A, B, and C) which is equally strong but appears in all channels. Scale bar = 100 μ m.
Techniques Used: Imaging, Labeling

Figure Legend Snippet: Quantification of m1 AChR expression by parvalbumin neurons. The graphs show the percentage of parvalbumin (PV) neurons encountered, by cortical layer, that were also immunoreactive for m1 AChRs in areas V1 (A) and the middle temporal visual area (MT) (B). Error bars represent SEM. Number of PV neurons in each graph is the same: V1 = 293 PV neurons, MT = 293 PV neurons.
Techniques Used: Expressing

Figure Legend Snippet: Quantification of the parvalbumin-immunoreactive population as a percentage of m1 AChR-expressing neurons. The graphs show the percentage of m1 AChR-expressing neurons encountered, by cortical layer, that were also immunoreactive for parvalbumin in areas V1 (A) and the middle temporal visual area (MT) (B). Error bars represent SEM. Number of m1 AChR-ir neurons: V1 = 520, MT = 1081.
Techniques Used: Expressing

Figure Legend Snippet: The distributions of soma sizes are similar between the populations of singly and dually labeled neurons in V1 (A) or the middle temporal visual area (MT) (B). In these histograms of soma sizes, measured along the long axis, it can be seen that in V1 (A) the distributions for singly-labeled parvalbumin (PV)- and m1 AChR-ir neurons, and for dually immunoreactive neurons are unimodal and centered around 12–14 microns. In MT these distributions are shifted to the right and somewhat skewed, with a long tail at the end representing soma sizes greater than 20 μ m. This tail of the distribution has a very small N , but all three groups (single PV-ir, single m1AChR-ir and dual PV/m1-ir) are represented in the population of neurons with large somata, offering no evidence for a bi-modal distribution of soma size in either cortical area. N for V1: m1 single = 52, PV single = 11, dual = 50 neurons. N for MT: m1 single = 52, PV single = 12, dual = 45 neurons.
Techniques Used: Labeling
m1 achr antibody (Alomone Labs)


Structured Review

M1 Achr Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/m1 achr antibody/product/Alomone Labs
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque"
Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque
Journal: Brain and Behavior
doi: 10.1002/brb3.225

Figure Legend Snippet: Qualitative detail of single-label immunoperoxidase reactivity for m1 ACh receptors, panels A and B) and parvalbumin (C and D) in visual areas V1 (A and C) and the middle temporal visual area (MT) (B and D). The micrograph in panel A shows m1 AChR-immunoreactivity in layer 5 of area V1. Panel B shows m1 AChR-immunoreactivity in layer 3 of MT. In both panels the characteristic stained cytoplasmic ring around an immunonegative nuclear region is evident (asterisks). When immunoreactive dendrites are evident, they are usually (arrowhead in A), but not always (arrowhead in B) visibly attached to a cell body. There was no axonal staining evident in either cortical area. Parvalbumin immunoreactivity (C and D) on the other hand, is evident in cell bodies, dendrites (arrowheads in C and D) and axons (arrows in D). Panel C is a micrograph captured in layer 2 of area V1. The parvalbumin immunoreactivity shown in Panel D is of layer 5 in MT. Scale bar = 20 μ m.
Techniques Used: Staining

Figure Legend Snippet: Most m1 AChR-immunoreactive neurons (panel B, magenta) in the middle temporal visual area (MT) are not immunoreactive for parvalbumin (PV; panel A, green). This image was captured in layer 5 of area MT using a 40× objective. There are seven PV neurons in the imaged field (+, A). Note that the cell body marked with a ∼ in panel A would not have been counted in this study as it does not have a clearly defined boundary within the imaging plane, although it is a PV neuron. Five of these seven PV neurons are also immunoreactive for the m1 AChR (+ in B and C). Two are m1-immunonegative (arrows in B). A striking feature of this image is the number of neurons that are immunoreactive for m1 AChRs (B, C), but not PV (A). Although these singly labeled m1-ir neurons occasionally appear pyramidal (*), it is generally not possible to determine cell morphology (or, therefore, cell class) from the immunoreactivity for m1 AChRs. The strongly fluorescent regions circled in B and C would not have been counted as they do not appear somatic in shape. These regions appear in only one channel and can thus be distinguished from the lipofuscin autofluorescence (∧ in A, B, and C) which is equally strong but appears in all channels. Scale bar = 100 μ m.
Techniques Used: Imaging, Labeling

Figure Legend Snippet: Quantification of m1 AChR expression by parvalbumin neurons. The graphs show the percentage of parvalbumin (PV) neurons encountered, by cortical layer, that were also immunoreactive for m1 AChRs in areas V1 (A) and the middle temporal visual area (MT) (B). Error bars represent SEM. Number of PV neurons in each graph is the same: V1 = 293 PV neurons, MT = 293 PV neurons.
Techniques Used: Expressing

Figure Legend Snippet: Quantification of the parvalbumin-immunoreactive population as a percentage of m1 AChR-expressing neurons. The graphs show the percentage of m1 AChR-expressing neurons encountered, by cortical layer, that were also immunoreactive for parvalbumin in areas V1 (A) and the middle temporal visual area (MT) (B). Error bars represent SEM. Number of m1 AChR-ir neurons: V1 = 520, MT = 1081.
Techniques Used: Expressing

Figure Legend Snippet: The distributions of soma sizes are similar between the populations of singly and dually labeled neurons in V1 (A) or the middle temporal visual area (MT) (B). In these histograms of soma sizes, measured along the long axis, it can be seen that in V1 (A) the distributions for singly-labeled parvalbumin (PV)- and m1 AChR-ir neurons, and for dually immunoreactive neurons are unimodal and centered around 12–14 microns. In MT these distributions are shifted to the right and somewhat skewed, with a long tail at the end representing soma sizes greater than 20 μ m. This tail of the distribution has a very small N , but all three groups (single PV-ir, single m1AChR-ir and dual PV/m1-ir) are represented in the population of neurons with large somata, offering no evidence for a bi-modal distribution of soma size in either cortical area. N for V1: m1 single = 52, PV single = 11, dual = 50 neurons. N for MT: m1 single = 52, PV single = 12, dual = 45 neurons.
Techniques Used: Labeling