rabbit antiserum against syntaxin 6 110062 Search Results


anti tgn46 antibody ahp500  (Bio-Rad)
96
Bio-Rad anti tgn46 antibody ahp500
Anti Tgn46 Antibody Ahp500, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+antiserum+against+syntaxin+6+110062/Sheep+anti+Human+TGN46/pm19192245-210-0-5
Average 96 stars, based on 1 article reviews
anti tgn46 antibody ahp500 - by Bioz Stars, 2026-09
96/100 stars
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human glut4 antibody  (Bio-Techne corporation)
92
Bio-Techne corporation human glut4 antibody
Human Glut4 Antibody, supplied by Bio-Techne corporation, 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/product/rabbit+antiserum+against+syntaxin+6+110062/Human+Glut4+Antibody/bio-techne+corporation___mab8654
Average 92 stars, based on 1 article reviews
human glut4 antibody - by Bioz Stars, 2026-09
92/100 stars
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clathrin heavy chain  (Proteintech)
96
Proteintech clathrin heavy chain
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Clathrin Heavy Chain, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+antiserum+against+syntaxin+6+110062/HRP-conjugated+Heavy+chain+of+Rabbit+IgG+Antibody/bio_rxiv__2025__06__27__661901-353-11-15
Average 96 stars, based on 1 article reviews
clathrin heavy chain - by Bioz Stars, 2026-09
96/100 stars
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mouse anti-syntaxin 6  (Becton Dickinson)
90
Becton Dickinson mouse anti-syntaxin 6
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Mouse Anti Syntaxin 6, supplied by Becton Dickinson, 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+antiserum+against+syntaxin+6+110062/mouse+anti+syntaxin+6+antibody/pm37355986-529-123-126
Average 90 stars, based on 1 article reviews
mouse anti-syntaxin 6 - by Bioz Stars, 2026-09
90/100 stars
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anti rab7  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc anti rab7
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Anti Rab7, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+antiserum+against+syntaxin+6+110062/Rab7+XP+Rabbit+mAb/pmc10954720-259-12-15
Average 96 stars, based on 1 article reviews
anti rab7 - by Bioz Stars, 2026-09
96/100 stars
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anti appl1  (Cell Signaling Technology Inc)
95
Cell Signaling Technology Inc anti appl1
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Anti Appl1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+antiserum+against+syntaxin+6+110062/APPL1+XP+Rabbit+mAb/pmc10954720-259-9-15
Average 95 stars, based on 1 article reviews
anti appl1 - by Bioz Stars, 2026-09
95/100 stars
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anti rabenosyn 5  (Proteintech)
93
Proteintech anti rabenosyn 5
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Anti Rabenosyn 5, supplied by Proteintech, 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+antiserum+against+syntaxin+6+110062/Rabenosyn+5+Antibody/pmc10954720-259-51-54
Average 93 stars, based on 1 article reviews
anti rabenosyn 5 - by Bioz Stars, 2026-09
93/100 stars
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rfp-booster atto580  (NanoTag Biotechnologies GmbH)
90
NanoTag Biotechnologies GmbH rfp-booster atto580
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Rfp Booster Atto580, supplied by NanoTag Biotechnologies GmbH, 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+antiserum+against+syntaxin+6+110062/rfp+booster+atto580/pm37355986-529-208-210
Average 90 stars, based on 1 article reviews
rfp-booster atto580 - by Bioz Stars, 2026-09
90/100 stars
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anti-rabbit-igg-hrp  (Biozol Diagnostica Vertrieb GmbH)
90
Biozol Diagnostica Vertrieb GmbH anti-rabbit-igg-hrp
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Anti Rabbit Igg Hrp, supplied by Biozol Diagnostica Vertrieb GmbH, 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+antiserum+against+syntaxin+6+110062/hrp+coupled+anti+rabbit+igg/pm37355986-529-200-201
Average 90 stars, based on 1 article reviews
anti-rabbit-igg-hrp - by Bioz Stars, 2026-09
90/100 stars
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rabbit anti rfp rockland  (Rockland Immunochemicals)
98
Rockland Immunochemicals rabbit anti rfp rockland
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Rabbit Anti Rfp Rockland, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+antiserum+against+syntaxin+6+110062/Anti-rfp/pm37355986-529-96-98
Average 98 stars, based on 1 article reviews
rabbit anti rfp rockland - by Bioz Stars, 2026-09
98/100 stars
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anti-mouse-igg-hrp  (Biozol Diagnostica Vertrieb GmbH)
90
Biozol Diagnostica Vertrieb GmbH anti-mouse-igg-hrp
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
Anti Mouse Igg Hrp, supplied by Biozol Diagnostica Vertrieb GmbH, 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+antiserum+against+syntaxin+6+110062/anti+mouse+igg+hrp/pm37355986-529-204-205
Average 90 stars, based on 1 article reviews
anti-mouse-igg-hrp - by Bioz Stars, 2026-09
90/100 stars
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40,6-diamidino-2-phenylindole (dapi  (Biozol Diagnostica Vertrieb GmbH)
90
Biozol Diagnostica Vertrieb GmbH 40,6-diamidino-2-phenylindole (dapi
The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with <t>clathrin,</t> helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific <t>membrane</t> <t>proteins</t> and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.
40,6 Diamidino 2 Phenylindole (Dapi, supplied by Biozol Diagnostica Vertrieb GmbH, 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+antiserum+against+syntaxin+6+110062/y27632/pm37355986-529-224-226
Average 90 stars, based on 1 article reviews
40,6-diamidino-2-phenylindole (dapi - by Bioz Stars, 2026-09
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Image Search Results


The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with clathrin, helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific membrane proteins and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.

Journal: bioRxiv

Article Title: AP-3 complex sorts preferential cargo to govern dense core vesicle function in neuroendocrine cells

doi: 10.1101/2025.06.27.661901

Figure Lengend Snippet: The presence of AP-3 at both the TGN and the endosomes gives rise to two plausible mechanisms of cargo sorting. At the TGN, AP-3, along with clathrin, helps form specific sorting sites where the DCV cargo is loaded into the immature DCVs. These immature DCVs then undergo homotypic fusion and mature, moving farther away from the TGN and getting docked at the plasma membrane for stimulus-coupled release. Alternatively, AP-3 present at the endosomes may be responsible for loading DCV cargo into the immature vesicles, thus making the DCVs more condensed and helping the maturation. AP-3 is also responsible for the budding of SLVs at the endosomes, the recycling of exocytotic vesicles and clearance via the Endolysosomal pathway. This figure shows the vesicle trafficking in WT PC12 cells compared to AP-3 KD cells. The absence of AP-3 is responsible for inhibiting the maturation of DCVs and may lead to stunted transport of specific membrane proteins and Cargo to the DCVs. Loss of AP-3 leads to the mis-sorting of membrane proteins to the lysosomes. Thus, it affects the regulated exocytosis of DCV at multiple checkpoints.

Article Snippet: The blots were processed accordingly and probed for targeted proteins CgB, Clathrin Heavy chain (CHC, Proteintech 26523-1-AP,1:2000), Syt1(Synaptic systems 105011,1:2500), ZnT3(Proteintech 17363-1-AP, 1:2500), Syntaxin 6(Synaptic systems 110062, 1:2000), VMAT1(Proteintech 20340-1-AP, 1:2000), AP3m1(Proteintech 12114-1-AP, 1:2000), Dlk1(Santa Cruz SC-25437,1:500).

Techniques: Clinical Proteomics, Membrane