m1 achr antibody  (Alomone Labs)


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    Structured Review

    Alomone Labs m1 achr antibody
    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 <t>m1</t> 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.
    M1 Achr Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/m1 achr antibody/product/Alomone Labs
    Average 91 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    m1 achr antibody - by Bioz Stars, 2022-09
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    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

    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.
    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

    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.
    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

    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.
    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

    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.
    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

    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.
    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

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    Alomone Labs human m1 achr
    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 <t>m1</t> 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.
    Human M1 Achr, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, 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 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    human m1 achr - by Bioz Stars, 2022-09
    93/100 stars
      Buy from Supplier

    91
    Alomone Labs m1 achr antibody
    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 <t>m1</t> 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.
    M1 Achr Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 91/100, 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 91 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    m1 achr antibody - by Bioz Stars, 2022-09
    91/100 stars
      Buy from Supplier

    Image Search Results


    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.

    Journal: Brain and Behavior

    Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque

    doi: 10.1002/brb3.225

    Figure Lengend 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.

    Article Snippet: We detected m1 muscarinic ACh receptors (m1 AChRs) using a polyclonal antibody raised in rabbit against amino acids 227–353 of the intracellular loop i3 of the human m1 AChR, obtained from Alomone Labs (Jerusalem, Israel, catalog #AMR-001, lot # AN-05).

    Techniques: Imaging, Labeling

    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.

    Journal: Brain and Behavior

    Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque

    doi: 10.1002/brb3.225

    Figure Lengend 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.

    Article Snippet: We detected m1 muscarinic ACh receptors (m1 AChRs) using a polyclonal antibody raised in rabbit against amino acids 227–353 of the intracellular loop i3 of the human m1 AChR, obtained from Alomone Labs (Jerusalem, Israel, catalog #AMR-001, lot # AN-05).

    Techniques: Expressing

    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.

    Journal: Brain and Behavior

    Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque

    doi: 10.1002/brb3.225

    Figure Lengend 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.

    Article Snippet: We detected m1 muscarinic ACh receptors (m1 AChRs) using a polyclonal antibody raised in rabbit against amino acids 227–353 of the intracellular loop i3 of the human m1 AChR, obtained from Alomone Labs (Jerusalem, Israel, catalog #AMR-001, lot # AN-05).

    Techniques: Expressing

    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.

    Journal: Brain and Behavior

    Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque

    doi: 10.1002/brb3.225

    Figure Lengend 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.

    Article Snippet: We detected m1 muscarinic ACh receptors (m1 AChRs) using a polyclonal antibody raised in rabbit against amino acids 227–353 of the intracellular loop i3 of the human m1 AChR, obtained from Alomone Labs (Jerusalem, Israel, catalog #AMR-001, lot # AN-05).

    Techniques: Labeling

    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.

    Journal: Brain and Behavior

    Article Title: Muscarinic acetylcholine receptors are expressed by most parvalbumin-immunoreactive neurons in area MT of the macaque

    doi: 10.1002/brb3.225

    Figure Lengend 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.

    Article Snippet: We detected m1 muscarinic ACh receptors (m1 AChRs) using a polyclonal antibody raised in rabbit against amino acids 227–353 of the intracellular loop i3 of the human m1 AChR, obtained from Alomone Labs (Jerusalem, Israel, catalog #AMR-001, lot # AN-05).

    Techniques: Staining