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na v 1 3 rb  (Alomone Labs)


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    Structured Review

    Alomone Labs na v 1 3 rb
    Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.
    Na V 1 3 Rb, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 33 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/asc-004/pmc12852067-3-0-5?v=Alomone+Labs
    Average 94 stars, based on 33 article reviews
    na v 1 3 rb - by Bioz Stars, 2026-07
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    Images

    1) Product Images from "Distribution of Voltage‐Gated Sodium Channels and Scaffolding Proteins on Vestibular Calyx Ending Delineates the Axon Initial Segment"

    Article Title: Distribution of Voltage‐Gated Sodium Channels and Scaffolding Proteins on Vestibular Calyx Ending Delineates the Axon Initial Segment

    Journal: The Journal of Comparative Neurology

    doi: 10.1002/cne.70127

    Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.
    Figure Legend Snippet: Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.

    Techniques Used: Staining, Labeling, Membrane, Immunostaining



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    Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.
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    Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.
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    Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.
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    Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.
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    Preliminary RW exercise redressed abnormal VGSCs protein expression of TBI mice. The expression of <t>Nav1.1</t> ( a – e ), Nav1.3 ( f – j ) and Nav1.6 ( k – o ) proteins in each group was treated with exercise pre-training at different periods, which indicated by western blotting assay. Data are expressed as Mean ± SD ( n = 9)
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    Image Search Results


    Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.

    Journal: The Journal of Comparative Neurology

    Article Title: Distribution of Voltage‐Gated Sodium Channels and Scaffolding Proteins on Vestibular Calyx Ending Delineates the Axon Initial Segment

    doi: 10.1002/cne.70127

    Figure Lengend Snippet: Na V 1.3 antibody labels Domain 3 in presumed C units. (A, A’) In this maximum intensity projection image of a stack from a crista, the presumption is based on the relatively superficial location of Caspr1‐stained hemi‐paranodes (red, arrows) and the location of the units in the CZ. Na V 1.3 labeling ( green in A’) is absent in the PZ ( not shown ), which contains D , but not C , units. In the three units marked by arrows in A, MBP ( blue ) can be traced from the parent axons below the basement membrane (BM) (dashed line) to the stained hemi‐paranodes. In A’, Caspr1 immunostaining ( red ) has been removed, leaving Na V 1.3 labeling ( green ) of Domain 3, including the outer surface of the calyx endings (COF, Domain 3a) and the unmyelinated parent axons above the heminodes (Domain 3b, locations indicated by arrows ). Inset, upper right , schematic of entire calyx, showing Domain 3 in red. (B, C) Additional examples of calyx afferents labeled with Na V 1.3. Same color conventions as in A. Scale bars = 5 µm.

    Article Snippet: Na V 1.3 (rb) , Alomone , ASC‐004 RRID:AB_2040007 , , X (DRG) , , X , X (w) , Datasheet.

    Techniques: Staining, Labeling, Membrane, Immunostaining

    Preliminary RW exercise redressed abnormal VGSCs protein expression of TBI mice. The expression of Nav1.1 ( a – e ), Nav1.3 ( f – j ) and Nav1.6 ( k – o ) proteins in each group was treated with exercise pre-training at different periods, which indicated by western blotting assay. Data are expressed as Mean ± SD ( n = 9)

    Journal: Experimental Brain Research

    Article Title: Voluntary running wheel exercise induces cognitive improvement post traumatic brain injury in mouse model through redressing aberrant excitation regulated by voltage-gated sodium channels 1.1, 1.3, and 1.6

    doi: 10.1007/s00221-023-06734-2

    Figure Lengend Snippet: Preliminary RW exercise redressed abnormal VGSCs protein expression of TBI mice. The expression of Nav1.1 ( a – e ), Nav1.3 ( f – j ) and Nav1.6 ( k – o ) proteins in each group was treated with exercise pre-training at different periods, which indicated by western blotting assay. Data are expressed as Mean ± SD ( n = 9)

    Article Snippet: Then, they were incubated against Nav1.1 (1:800; cat. no. ASC-001; Alomone), Nav1.3 (1:500; cat. no. ASC-004; Alomone), or Nav1.6 (1:600; cat. no. ASC-009; Alomone) using antibodies.

    Techniques: Expressing, Western Blot

    Either voluntary RW before TBI or prior-injury combined with post-injury exercise training redressed abnormal VGSCs protein expression of TBI mice. a – c The expression of Nav1.1, Nav1.3, Nav1.6 transmembrane protein in preliminary voluntary RW group. d – f The expression of Nav1.1, Nav1.3, Nav1.6 transmembrane protein in pre-training combined with TBI post-injury exercise training group. Data are expressed as Means ± SD ( n = 9)

    Journal: Experimental Brain Research

    Article Title: Voluntary running wheel exercise induces cognitive improvement post traumatic brain injury in mouse model through redressing aberrant excitation regulated by voltage-gated sodium channels 1.1, 1.3, and 1.6

    doi: 10.1007/s00221-023-06734-2

    Figure Lengend Snippet: Either voluntary RW before TBI or prior-injury combined with post-injury exercise training redressed abnormal VGSCs protein expression of TBI mice. a – c The expression of Nav1.1, Nav1.3, Nav1.6 transmembrane protein in preliminary voluntary RW group. d – f The expression of Nav1.1, Nav1.3, Nav1.6 transmembrane protein in pre-training combined with TBI post-injury exercise training group. Data are expressed as Means ± SD ( n = 9)

    Article Snippet: Then, they were incubated against Nav1.1 (1:800; cat. no. ASC-001; Alomone), Nav1.3 (1:500; cat. no. ASC-004; Alomone), or Nav1.6 (1:600; cat. no. ASC-009; Alomone) using antibodies.

    Techniques: Expressing

    Exercise-conditioned serum treatment redressed the abnormal expressions of Nav1.1, Nav1.3, Nav1.6 proteins in cortical neurons. The Nav1.1 protein expression showed in ( a – c ), the Nav1.3 protein expression showed in (d-f), while the Nav1.6 protein expression showed in ( g – i ). Data are expressed as Mean ± SD ( n = 7)

    Journal: Experimental Brain Research

    Article Title: Voluntary running wheel exercise induces cognitive improvement post traumatic brain injury in mouse model through redressing aberrant excitation regulated by voltage-gated sodium channels 1.1, 1.3, and 1.6

    doi: 10.1007/s00221-023-06734-2

    Figure Lengend Snippet: Exercise-conditioned serum treatment redressed the abnormal expressions of Nav1.1, Nav1.3, Nav1.6 proteins in cortical neurons. The Nav1.1 protein expression showed in ( a – c ), the Nav1.3 protein expression showed in (d-f), while the Nav1.6 protein expression showed in ( g – i ). Data are expressed as Mean ± SD ( n = 7)

    Article Snippet: Then, they were incubated against Nav1.1 (1:800; cat. no. ASC-001; Alomone), Nav1.3 (1:500; cat. no. ASC-004; Alomone), or Nav1.6 (1:600; cat. no. ASC-009; Alomone) using antibodies.

    Techniques: Expressing