bait vector pas2 1 Search Results


two hybrid y2h bait vector pas2 1  (TaKaRa)
96
TaKaRa two hybrid y2h bait vector pas2 1
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Two Hybrid Y2h Bait Vector Pas2 1, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bait vector pas2 1  (TaKaRa)
86
TaKaRa bait vector pas2 1
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Bait Vector Pas2 1, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bait vector pas2-1  (Promega)
90
Promega bait vector pas2-1
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Bait Vector Pas2 1, supplied by Promega, 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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pas2 1 vector  (TaKaRa)
96
TaKaRa pas2 1 vector
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Pas2 1 Vector, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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domain fusion pas2 1 vector  (TaKaRa)
99
TaKaRa domain fusion pas2 1 vector
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Domain Fusion Pas2 1 Vector, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pas2-1 vector  (Becton Dickinson)
90
Becton Dickinson pas2-1 vector
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Pas2 1 Vector, 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
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bait vector  (TaKaRa)
86
TaKaRa bait vector
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Bait Vector, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bait vector - by Bioz Stars, 2026-03
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vector pas2 1  (TaKaRa)
86
TaKaRa vector pas2 1
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Vector Pas2 1, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pas2 1  (TaKaRa)
86
TaKaRa pas2 1
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Pas2 1, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bait vectors plexa  (TaKaRa)
86
TaKaRa bait vectors plexa
Identification of I-2 domains required for yeast two-hybrid <t>(Y2H)</t> interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and <t>pAS2-1</t> empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.
Bait Vectors Plexa, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Identification of I-2 domains required for yeast two-hybrid (Y2H) interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and pAS2-1 empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.

Journal: Journal of Experimental Botany

Article Title: Protein–protein interactions as a proxy to monitor conformational changes and activation states of the tomato resistance protein I-2

doi: 10.1093/jxb/ers021

Figure Lengend Snippet: Identification of I-2 domains required for yeast two-hybrid (Y2H) interaction with I2I-1 and I2I-2. (A) Y2H analyses show interactions of I2I-1 or I2I-2 with full-length I-2 as bait, but not with Rx and Mi-1.2. I2I-1 and I2I-2 interact with the CC-NB-ARC bait of I-2 (amino acids 1–520), but not with bait constructs containing the CC-NB-ARC domains of I-2C1 (amino acids 1–526), Rx (amino acids 1–426), or Mi-1.2 (amino acids 161–896). The baits and preys did not show autoactivity when co-expressed with the pACT2 and pAS2-1 empty vectors. The test for activation of the HIS3 marker is shown after 10 days of growth (left panel). Expression of the bait proteins was confirmed by Western blot (WB) analyses using α-Gal4BD antibody detection on total yeast protein extracts (right panel). (B) Y2H analyses of I2I-1 and I2I-2 with various I-2 baits: I-2FL (full-length: amino acids 1–1266), I-2N+ (amino acids 1–643), I-2N (amino acids 1–520), I-2N ΔMHD (amino acids 1–520, with deletion at amino acids 484–496), and I-2CC (amino acids 1–170). The different I-2 (sub)domains are indicated and coloured: orange, coiled-coil (CC); red, nucleotide-binding (NB); purple, Apaf-1, R proteins, and Ced-4 (ARC) 1; blue, ARC2; and green, leucine-rich repeat (LRR). The test for activation of the ADE2 marker is shown after 5 days of growth; the other two markers ( HIS3, LacZ ) gave identical results. +, activation of all three selectable markers; –, no activation of these markers. The smallest part of I-2 enabling interaction with I2I-1 is the CC domain and for I2I-2 the CC-NB-ARC domain.

Article Snippet: The bait used for the library screen was constructed by subcloning the Nco I/ Sac I fragment of I-2 FL in the yeast two-hybrid (Y2H) bait vector pAS2-1 (Clontech Laboratories, Palo Alto, CA, USA), resulting in bait CC-NB-ARC-LRR1-12 (amino acids 1–872).

Techniques: Construct, Activation Assay, Marker, Expressing, Western Blot, Binding Assay