rabbit anti bmpr 1b Search Results


mouse anti bmpr 1b  (R&D Systems)
93
R&D Systems mouse anti bmpr 1b
Mouse Anti Bmpr 1b, supplied by R&D Systems, 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/product/rabbit+anti+bmpr+1b/Human%2FMouse+BMPR-IB%2FALK-6+Antibody/pm37279475-170-32-36
Average 93 stars, based on 1 article reviews
mouse anti bmpr 1b - by Bioz Stars, 2026-09
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rabbit anti-k v 3.1b  (Merck KGaA)
90
Merck KGaA rabbit anti-k v 3.1b
Rabbit Anti K V 3.1b, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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rabbit anti-kv3.1b  (GeneTex)
90
GeneTex rabbit anti-kv3.1b
<t>Kv3.4</t> in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, <t>Kv3.1b-IR</t> is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.
Rabbit Anti Kv3.1b, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+bmpr+1b/rabbit+anti+kv3+1b/pmc06596659-575-1-6
Average 90 stars, based on 1 article reviews
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kv3 1 b  (NeuroMab)
92
NeuroMab kv3 1 b
<t>Kv3.4</t> in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, <t>Kv3.1b-IR</t> is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.
Kv3 1 B, supplied by NeuroMab, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
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rabbit anti il 1b  (Genzyme)
86
Genzyme rabbit anti il 1b
<t>Kv3.4</t> in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, <t>Kv3.1b-IR</t> is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.
Rabbit Anti Il 1b, supplied by Genzyme, 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/product/rabbit+anti+bmpr+1b/1+anti+il+mouse+polyclonal+rabbit/pm01906353-61-12-14
Average 86 stars, based on 1 article reviews
rabbit anti il 1b - by Bioz Stars, 2026-09
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rabbit anti-v 1b r  (International Laboratory USA)
90
International Laboratory USA rabbit anti-v 1b r
<t>Kv3.4</t> in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, <t>Kv3.1b-IR</t> is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.
Rabbit Anti V 1b R, supplied by International Laboratory USA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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rabbit polyclonal anti-sr-1b antibody  (Bioworld Antibodies)
90
Bioworld Antibodies rabbit polyclonal anti-sr-1b antibody
<t>Kv3.4</t> in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, <t>Kv3.1b-IR</t> is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.
Rabbit Polyclonal Anti Sr 1b Antibody, supplied by Bioworld Antibodies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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kv3 1b  (Alomone Labs)
94
Alomone Labs kv3 1b
<t>Kv3.4</t> in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, <t>Kv3.1b-IR</t> is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.
Kv3 1b, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+bmpr+1b/Anti-Kv3%2E1b+(KCNC1)+Antibody/10__1523_slash_jneurosci__3437___15__2016-51-22-24
Average 94 stars, based on 1 article reviews
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rabbit anti-rat il-1b  (Abfrontier ltd)
90
Abfrontier ltd rabbit anti-rat il-1b
<t>Kv3.4</t> in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, <t>Kv3.1b-IR</t> is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.
Rabbit Anti Rat Il 1b, supplied by Abfrontier ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+bmpr+1b/rabbit+anti+rat+il+1b/10__1016_slash_j__joca__2012__02__021-86-12-15
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rabbit polyclonal anti xxiii antibody 6 1 b  (Santa Cruz Biotechnology)
92
Santa Cruz Biotechnology rabbit polyclonal anti xxiii antibody 6 1 b
FIG. 7. Immunoblot analysis of collagen XXIII. Lysate was pre- pared from AT2.1 Dunning rat prostate carcinoma cells transfected with empty vector (lane 1) or collagen XXIII(del1–48)Myc (lane 2), separated by 8% SDS-PAGE, and immunoblotted with rabbit <t>polyclonal</t> antibody 6.1B raised against the carboxyl terminus of collagen XXIII (A), or 9E10 monoclonal anti-Myc antibody (B). C, analysis of 100 g of cell lysate separated by 6% SDS-PAGE and immunoblotted with 6.1B antibody indicates expression of the 75-kDa collagen XXIII protein in AT6.1 cells and MatLyLu cells, marked by an arrowhead. Molecular mass markers (kDa) are shown on the left.
Rabbit Polyclonal Anti Xxiii Antibody 6 1 B, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rabbit-anti-il-1b  (GeneTex)
90
GeneTex rabbit-anti-il-1b
FIG. 7. Immunoblot analysis of collagen XXIII. Lysate was pre- pared from AT2.1 Dunning rat prostate carcinoma cells transfected with empty vector (lane 1) or collagen XXIII(del1–48)Myc (lane 2), separated by 8% SDS-PAGE, and immunoblotted with rabbit <t>polyclonal</t> antibody 6.1B raised against the carboxyl terminus of collagen XXIII (A), or 9E10 monoclonal anti-Myc antibody (B). C, analysis of 100 g of cell lysate separated by 6% SDS-PAGE and immunoblotted with 6.1B antibody indicates expression of the 75-kDa collagen XXIII protein in AT6.1 cells and MatLyLu cells, marked by an arrowhead. Molecular mass markers (kDa) are shown on the left.
Rabbit Anti Il 1b, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti homer 1b c  (Santa Cruz Biotechnology)
94
Santa Cruz Biotechnology anti homer 1b c
FIG. 7. Immunoblot analysis of collagen XXIII. Lysate was pre- pared from AT2.1 Dunning rat prostate carcinoma cells transfected with empty vector (lane 1) or collagen XXIII(del1–48)Myc (lane 2), separated by 8% SDS-PAGE, and immunoblotted with rabbit <t>polyclonal</t> antibody 6.1B raised against the carboxyl terminus of collagen XXIII (A), or 9E10 monoclonal anti-Myc antibody (B). C, analysis of 100 g of cell lysate separated by 6% SDS-PAGE and immunoblotted with 6.1B antibody indicates expression of the 75-kDa collagen XXIII protein in AT6.1 cells and MatLyLu cells, marked by an arrowhead. Molecular mass markers (kDa) are shown on the left.
Anti Homer 1b C, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Kv3.4 in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, Kv3.1b-IR is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.

Journal: The Journal of Neuroscience

Article Title: K + Channel Kv3.4 Is Essential for Axon Growth by Limiting the Influx of Ca 2+ into Growth Cones

doi: 10.1523/JNEUROSCI.1076-16.2017

Figure Lengend Snippet: Kv3.4 in the axonal growth cones of dorsal spinal commissural neurons. A–F, Transverse sections of the spinal cord of chick embryos were immunostained for Kv3.4. A, Absence of Kv3.4-IR in the dorsal spinal cord at HH17. Kv3.4-IR in precrossing commissural axons (B–F, arrowheads) is evident during HH19-HH25 but disappears at HH27. D, Arrows indicate postcrossing commissural axons projecting from the other side of spinal cord. FP, Floor plate. G–L, Transverse sections of the spinal cord at HH23 were immunostained as indicated. G, Absence of Kv1.5-IR. H, Kv4.2-IR in the somata and dendrites of motoneurons (MN). I, Kv4.3-IR in the bifurcation zone (BZ). In addition to the BZ, Kv3.1b-IR is strong in postcrossing commissural axons (J, arrow) but weak in precrossing commissural axons (J, arrowhead). K, Absence of Kv3.2-IR. L, Kv3.3 in motoneurons. M–M″, Double staining in transverse sections of the spinal cord at HH21 shows colocalization of Kv3.4 and axonin-1 in the growth cones (arrowheads) of commissural axons. N–N″, Colocalization of Kv3.4 and axonin-1 in cultured dorsal spinal neurons isolated from HH21-HH23 chick embryos. O–P″, Red fluorescence-tagged phalloidin colabeling reveals enrichment of Kv3.4 in the growth cone (O–O″) and Kv3.1b in the soma/axon shaft (P–P″) of cultured dorsal spinal neurons. Q–Q″, Kv3.4 and DiI colabeling. White represents Kv3.4-abundant regions. Blue represents Kv3.4-sparse regions (Q″). R, Ratio of Kv3.4/DiI in the soma, axon shaft, or growth cone of each neuron was obtained by dividing the fluorescence intensity of Kv3.4 by that of DiI. Data are mean ± SEM (n = 8 neurons, pooled from three independent experiments done on different days). ***p < 0.001, comparison of the indicated pairs (Tukey's post hoc test after one-way ANOVA). S–U, Kv3.4-IR in spinal commissural axons (arrowheads) of rat embryos is evident during E12.5-E13.5 (S, T), but it disappears at E14.5 (U). Scale bar: (in U) A, B, 35 μm; C, D, 40 μm; E, 50 μm; F, 60 μm; G–L, 50 μm; M–M″, 30 μm; N–N″, 13 μm; O–O″, 20 μm; P–P″, 20 μm; Q–Q″, 16 μm; S–U, 100 μm.

Article Snippet: Rabbit anti-Kv3.1b (custom-made and affinity-purified by GeneTex; RRID:AB_2566819) was raised against the peptide (C)DQALTPDEGLPFTRS corresponding to amino acids 523–537 of rat Kv3.1b, with an extra cysteine added to the N terminus.

Techniques: Double Staining, Cell Culture, Isolation, Fluorescence

FIG. 7. Immunoblot analysis of collagen XXIII. Lysate was pre- pared from AT2.1 Dunning rat prostate carcinoma cells transfected with empty vector (lane 1) or collagen XXIII(del1–48)Myc (lane 2), separated by 8% SDS-PAGE, and immunoblotted with rabbit polyclonal antibody 6.1B raised against the carboxyl terminus of collagen XXIII (A), or 9E10 monoclonal anti-Myc antibody (B). C, analysis of 100 g of cell lysate separated by 6% SDS-PAGE and immunoblotted with 6.1B antibody indicates expression of the 75-kDa collagen XXIII protein in AT6.1 cells and MatLyLu cells, marked by an arrowhead. Molecular mass markers (kDa) are shown on the left.

Journal: Journal of Biological Chemistry

Article Title: Type XXIII Collagen, a New Transmembrane Collagen Identified in Metastatic Tumor Cells

doi: 10.1074/jbc.m210616200

Figure Lengend Snippet: FIG. 7. Immunoblot analysis of collagen XXIII. Lysate was pre- pared from AT2.1 Dunning rat prostate carcinoma cells transfected with empty vector (lane 1) or collagen XXIII(del1–48)Myc (lane 2), separated by 8% SDS-PAGE, and immunoblotted with rabbit polyclonal antibody 6.1B raised against the carboxyl terminus of collagen XXIII (A), or 9E10 monoclonal anti-Myc antibody (B). C, analysis of 100 g of cell lysate separated by 6% SDS-PAGE and immunoblotted with 6.1B antibody indicates expression of the 75-kDa collagen XXIII protein in AT6.1 cells and MatLyLu cells, marked by an arrowhead. Molecular mass markers (kDa) are shown on the left.

Article Snippet: Immunoblotting was performed using rabbit polyclonal anti-XXIII antibody 6.1B or 9E10 anti-Myc antibody (Santa Cruz), followed by horseradish peroxidase-conjugated secondary antibodies (Amersham Biosciences) and detected by an enhanced chemiluminescence detection system (PerkinElmer Life Sciences).

Techniques: Western Blot, Transfection, Plasmid Preparation, SDS Page, Expressing