MedChemExpress transwell splenocytes
Transwell Splenocytes, supplied by MedChemExpress, 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 polyclonal anti mid1 (Novus Biologicals)

Novus Biologicals rabbit polyclonal anti mid1
EB1, <t>MID1,</t> and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

EB1, <t>MID1,</t> and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

Figure S7 D) ( N = 10–26 cells, n = 2 independent experiments). (C) EGFP-eLis1 (green) and LEs (LysoTracker, blue) localization in relation to eEB1-mScarlet, mScarlet-eCEP169, and mScarlet-eMID1 (red) ( B–S14D). (D) 30-s kymographs of EGFP-eLis1, eEB1-mScarlet, and LysoTracker of area in (C) (dotted line). (E) DyneinHC-positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 H) ( N = 13–18 cells, n = 2 independent experiments). (F) p150 glued -positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 J) ( N = 14–15 cells, n = 2 independent experiments). (G) HA-RILP (unstained) overexpression in mScarlet-eDyneinHC, EGFP-Lis1, or EGFP-ep150 glued cells (green), fixed and antibody-stained for CD63 (red). (H) Manders quantification of data in (G) ( N = 14–21 cells, n = 2 independent experiments). (I) EGFP-eLis1 (green) and mScarlet-eRab5a, mScarlet-eRab6a, or mScarlet-Rab7a (red) in time . (J) Distance quantification of data in (I). Measured is the shortest distance from detected vesicles to the Lis1-positive mask. Percentage of endosomes with distance <180 nm is plotted ( N = 20–31 cells, n = 3 independent experiments). Plots report mean; error bars reflect ± SD. t test or one-way ANOVA, ∗∗∗ p < 0.001, ∗∗ p < 0.005; ns, not significant. Scale bars as indicated. See also Figure S7 and and . " width="250" height="auto" />
Rabbit Polyclonal Anti Mid1, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mpg (Proteintech)

Proteintech mpg
EB1, <t>MID1,</t> and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

Figure S7 D) ( N = 10–26 cells, n = 2 independent experiments). (C) EGFP-eLis1 (green) and LEs (LysoTracker, blue) localization in relation to eEB1-mScarlet, mScarlet-eCEP169, and mScarlet-eMID1 (red) ( B–S14D). (D) 30-s kymographs of EGFP-eLis1, eEB1-mScarlet, and LysoTracker of area in (C) (dotted line). (E) DyneinHC-positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 H) ( N = 13–18 cells, n = 2 independent experiments). (F) p150 glued -positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 J) ( N = 14–15 cells, n = 2 independent experiments). (G) HA-RILP (unstained) overexpression in mScarlet-eDyneinHC, EGFP-Lis1, or EGFP-ep150 glued cells (green), fixed and antibody-stained for CD63 (red). (H) Manders quantification of data in (G) ( N = 14–21 cells, n = 2 independent experiments). (I) EGFP-eLis1 (green) and mScarlet-eRab5a, mScarlet-eRab6a, or mScarlet-Rab7a (red) in time . (J) Distance quantification of data in (I). Measured is the shortest distance from detected vesicles to the Lis1-positive mask. Percentage of endosomes with distance <180 nm is plotted ( N = 20–31 cells, n = 3 independent experiments). Plots report mean; error bars reflect ± SD. t test or one-way ANOVA, ∗∗∗ p < 0.001, ∗∗ p < 0.005; ns, not significant. Scale bars as indicated. See also Figure S7 and and . " width="250" height="auto" />
Mpg, 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
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60 aa (Addgene inc)

Addgene inc 60 aa
EB1, <t>MID1,</t> and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

Figure S7 D) ( N = 10–26 cells, n = 2 independent experiments). (C) EGFP-eLis1 (green) and LEs (LysoTracker, blue) localization in relation to eEB1-mScarlet, mScarlet-eCEP169, and mScarlet-eMID1 (red) ( B–S14D). (D) 30-s kymographs of EGFP-eLis1, eEB1-mScarlet, and LysoTracker of area in (C) (dotted line). (E) DyneinHC-positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 H) ( N = 13–18 cells, n = 2 independent experiments). (F) p150 glued -positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 J) ( N = 14–15 cells, n = 2 independent experiments). (G) HA-RILP (unstained) overexpression in mScarlet-eDyneinHC, EGFP-Lis1, or EGFP-ep150 glued cells (green), fixed and antibody-stained for CD63 (red). (H) Manders quantification of data in (G) ( N = 14–21 cells, n = 2 independent experiments). (I) EGFP-eLis1 (green) and mScarlet-eRab5a, mScarlet-eRab6a, or mScarlet-Rab7a (red) in time . (J) Distance quantification of data in (I). Measured is the shortest distance from detected vesicles to the Lis1-positive mask. Percentage of endosomes with distance <180 nm is plotted ( N = 20–31 cells, n = 3 independent experiments). Plots report mean; error bars reflect ± SD. t test or one-way ANOVA, ∗∗∗ p < 0.001, ∗∗ p < 0.005; ns, not significant. Scale bars as indicated. See also Figure S7 and and . " width="250" height="auto" />
60 Aa, supplied by Addgene inc, 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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primary antibodies against mid1ip1 (Proteintech)

Proteintech primary antibodies against mid1ip1
EB1, <t>MID1,</t> and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

Figure S7 D) ( N = 10–26 cells, n = 2 independent experiments). (C) EGFP-eLis1 (green) and LEs (LysoTracker, blue) localization in relation to eEB1-mScarlet, mScarlet-eCEP169, and mScarlet-eMID1 (red) ( B–S14D). (D) 30-s kymographs of EGFP-eLis1, eEB1-mScarlet, and LysoTracker of area in (C) (dotted line). (E) DyneinHC-positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 H) ( N = 13–18 cells, n = 2 independent experiments). (F) p150 glued -positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 J) ( N = 14–15 cells, n = 2 independent experiments). (G) HA-RILP (unstained) overexpression in mScarlet-eDyneinHC, EGFP-Lis1, or EGFP-ep150 glued cells (green), fixed and antibody-stained for CD63 (red). (H) Manders quantification of data in (G) ( N = 14–21 cells, n = 2 independent experiments). (I) EGFP-eLis1 (green) and mScarlet-eRab5a, mScarlet-eRab6a, or mScarlet-Rab7a (red) in time . (J) Distance quantification of data in (I). Measured is the shortest distance from detected vesicles to the Lis1-positive mask. Percentage of endosomes with distance <180 nm is plotted ( N = 20–31 cells, n = 3 independent experiments). Plots report mean; error bars reflect ± SD. t test or one-way ANOVA, ∗∗∗ p < 0.001, ∗∗ p < 0.005; ns, not significant. Scale bars as indicated. See also Figure S7 and and . " width="250" height="auto" />
Primary Antibodies Against Mid1ip1, 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
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mouse egfp id1 fusion protein (Addgene inc)

Addgene inc mouse egfp id1 fusion protein
EB1, <t>MID1,</t> and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

Figure S7 D) ( N = 10–26 cells, n = 2 independent experiments). (C) EGFP-eLis1 (green) and LEs (LysoTracker, blue) localization in relation to eEB1-mScarlet, mScarlet-eCEP169, and mScarlet-eMID1 (red) ( B–S14D). (D) 30-s kymographs of EGFP-eLis1, eEB1-mScarlet, and LysoTracker of area in (C) (dotted line). (E) DyneinHC-positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 H) ( N = 13–18 cells, n = 2 independent experiments). (F) p150 glued -positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 J) ( N = 14–15 cells, n = 2 independent experiments). (G) HA-RILP (unstained) overexpression in mScarlet-eDyneinHC, EGFP-Lis1, or EGFP-ep150 glued cells (green), fixed and antibody-stained for CD63 (red). (H) Manders quantification of data in (G) ( N = 14–21 cells, n = 2 independent experiments). (I) EGFP-eLis1 (green) and mScarlet-eRab5a, mScarlet-eRab6a, or mScarlet-Rab7a (red) in time . (J) Distance quantification of data in (I). Measured is the shortest distance from detected vesicles to the Lis1-positive mask. Percentage of endosomes with distance <180 nm is plotted ( N = 20–31 cells, n = 3 independent experiments). Plots report mean; error bars reflect ± SD. t test or one-way ANOVA, ∗∗∗ p < 0.001, ∗∗ p < 0.005; ns, not significant. Scale bars as indicated. See also Figure S7 and and . " width="250" height="auto" />
Mouse Egfp Id1 Fusion Protein, supplied by Addgene inc, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gene exp mid1 hs00931793 m1 (Thermo Fisher)

Thermo Fisher gene exp mid1 hs00931793 m1
EB1, <t>MID1,</t> and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

Figure S7 D) ( N = 10–26 cells, n = 2 independent experiments). (C) EGFP-eLis1 (green) and LEs (LysoTracker, blue) localization in relation to eEB1-mScarlet, mScarlet-eCEP169, and mScarlet-eMID1 (red) ( B–S14D). (D) 30-s kymographs of EGFP-eLis1, eEB1-mScarlet, and LysoTracker of area in (C) (dotted line). (E) DyneinHC-positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 H) ( N = 13–18 cells, n = 2 independent experiments). (F) p150 glued -positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 J) ( N = 14–15 cells, n = 2 independent experiments). (G) HA-RILP (unstained) overexpression in mScarlet-eDyneinHC, EGFP-Lis1, or EGFP-ep150 glued cells (green), fixed and antibody-stained for CD63 (red). (H) Manders quantification of data in (G) ( N = 14–21 cells, n = 2 independent experiments). (I) EGFP-eLis1 (green) and mScarlet-eRab5a, mScarlet-eRab6a, or mScarlet-Rab7a (red) in time . (J) Distance quantification of data in (I). Measured is the shortest distance from detected vesicles to the Lis1-positive mask. Percentage of endosomes with distance <180 nm is plotted ( N = 20–31 cells, n = 3 independent experiments). Plots report mean; error bars reflect ± SD. t test or one-way ANOVA, ∗∗∗ p < 0.001, ∗∗ p < 0.005; ns, not significant. Scale bars as indicated. See also Figure S7 and and . " width="250" height="auto" />
Gene Exp Mid1 Hs00931793 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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copy number variation mid1 hs02784563 cn (Thermo Fisher)

Thermo Fisher copy number variation mid1 hs02784563 cn

Copy Number Variation Mid1 Hs02784563 Cn, supplied by Thermo Fisher, 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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anti mid1 bethyl (Bethyl)

Bethyl anti mid1 bethyl

Anti Mid1 Bethyl, supplied by Bethyl, 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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anti mid1 (Boster Bio)

Boster Bio anti mid1

Anti Mid1, supplied by Boster Bio, 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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mid 1 (Cusabio)

Cusabio mid 1

Mid 1, supplied by Cusabio, 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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copy number variation mid1 hs02158662 cn (Thermo Fisher)

Thermo Fisher copy number variation mid1 hs02158662 cn

Copy Number Variation Mid1 Hs02158662 Cn, supplied by Thermo Fisher, 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

EB1, MID1, and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( <xref ref-type=

Journal: Current Biology

Article Title: Systems mapping of bidirectional endosomal transport through the crowded cell

doi: 10.1016/j.cub.2024.08.026

Figure Lengend Snippet: EB1, MID1, and CEP169 recruit Lis1 and dyneinHC, but not p150 glued , to the microtubule growing plus ends (A) EGFP-eLis1 (green) and SPYtubulin (red) localization in MelJuSo cells. Arrows show microtubule plus ends ( A). (B) Lis1-positive spots/μm 2 after indicated MAPs’ depletion compared with control (siC) ( Figure S7 D) ( N = 10–26 cells, n = 2 independent experiments). (C) EGFP-eLis1 (green) and LEs (LysoTracker, blue) localization in relation to eEB1-mScarlet, mScarlet-eCEP169, and mScarlet-eMID1 (red) ( B–S14D). (D) 30-s kymographs of EGFP-eLis1, eEB1-mScarlet, and LysoTracker of area in (C) (dotted line). (E) DyneinHC-positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 H) ( N = 13–18 cells, n = 2 independent experiments). (F) p150 glued -positive spots/μm 2 after indicated MAPs’ depletion, compared with control (siC) ( Figure S7 J) ( N = 14–15 cells, n = 2 independent experiments). (G) HA-RILP (unstained) overexpression in mScarlet-eDyneinHC, EGFP-Lis1, or EGFP-ep150 glued cells (green), fixed and antibody-stained for CD63 (red). (H) Manders quantification of data in (G) ( N = 14–21 cells, n = 2 independent experiments). (I) EGFP-eLis1 (green) and mScarlet-eRab5a, mScarlet-eRab6a, or mScarlet-Rab7a (red) in time . (J) Distance quantification of data in (I). Measured is the shortest distance from detected vesicles to the Lis1-positive mask. Percentage of endosomes with distance <180 nm is plotted ( N = 20–31 cells, n = 3 independent experiments). Plots report mean; error bars reflect ± SD. t test or one-way ANOVA, ∗∗∗ p < 0.001, ∗∗ p < 0.005; ns, not significant. Scale bars as indicated. See also Figure S7 and and .

Article Snippet: Rabbit polyclonal anti-MID1 , Novus , Cat#NBP1-26612; RRID: AB_1853386.

Techniques: Control, Over Expression, Staining

Journal: Current Biology

Article Title: Systems mapping of bidirectional endosomal transport through the crowded cell

doi: 10.1016/j.cub.2024.08.026

Figure Lengend Snippet:

Article Snippet: Rabbit polyclonal anti-MID1 , Novus , Cat#NBP1-26612; RRID: AB_1853386.

Techniques: Recombinant, CRISPR, Sequencing, Introduce, Clone Assay, Software

Journal: Current Biology

Article Title: Systems mapping of bidirectional endosomal transport through the crowded cell

doi: 10.1016/j.cub.2024.08.026

Figure Lengend Snippet:

Article Snippet: Rabbit polyclonal anti-MID1 , Novus , Cat#NBP1-26612; RRID: AB_1853386.

Techniques:

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: Known CHD risk genes

Article Snippet: , , , , , Hs02784563_cn , , , .

Techniques: Retroviral, Sequencing, Virus, Reverse Transcription

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: Case reports of likely causal CNVs

Article Snippet: , , , , , Hs02784563_cn , , , .

Techniques:

CHD-associated gene regions significantly enriched with large, rare CNVs

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: CHD-associated gene regions significantly enriched with large, rare CNVs

Article Snippet: , , , , , Hs02784563_cn , , , .

Techniques:

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: Enriched syndrome genes

Article Snippet: , , , , , Hs02784563_cn , , , .

Techniques:

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: Known CHD risk genes

Article Snippet: MID1 , MIDLINE 1 , Xp22.2 , 10373595 , 388135 , Hs02158662_cn , S , 300552 , 12833403, 20193066.

Techniques: Retroviral, Sequencing, Virus, Reverse Transcription

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: Case reports of likely causal CNVs

Article Snippet: MID1 , MIDLINE 1 , Xp22.2 , 10373595 , 388135 , Hs02158662_cn , S , 300552 , 12833403, 20193066.

Techniques:

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: CHD-associated gene regions significantly enriched with large, rare CNVs

Article Snippet: MID1 , MIDLINE 1 , Xp22.2 , 10373595 , 388135 , Hs02158662_cn , S , 300552 , 12833403, 20193066.

Techniques:

Journal: Physiological Genomics

Article Title: Human gene copy number spectra analysis in congenital heart malformations

doi: 10.1152/physiolgenomics.00013.2012

Figure Lengend Snippet: Enriched syndrome genes

Article Snippet: MID1 , MIDLINE 1 , Xp22.2 , 10373595 , 388135 , Hs02158662_cn , S , 300552 , 12833403, 20193066.

Techniques:

mid1 Search Results

Image Search Results