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Mouse anti γ adaptin

Manufactured by BD

Mouse anti-γ-adaptin is a laboratory reagent used to detect the gamma subunit of the adaptor protein complex AP-1 in various cell and tissue samples. It is a mouse monoclonal antibody that specifically binds to the gamma-adaptin protein, which is a key component of the AP-1 complex involved in the sorting and trafficking of proteins within the cell.

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5 protocols using mouse anti γ adaptin

1

Antibody Sources for Neuroscience Research

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The antibodies used in this study and their sources are as follows: rabbit anti-MAP2 (Santa Cruz Biotechnology, Dallas, TX); goat anti–ankyrin G (Santa Cruz Biotechnology); chicken anti-GFP (Invitrogen, Carlsbad, CA); mouse anti-TGN38 (Thermo Scientific, Rockford, IL); mouse anti–γ-adaptin (BD Biosciences, San Diego, CA); mouse anti-HA (Covance, Dedham, MA); chicken anti-HA (Millipore, Billerica, MA); chicken anti-MAP2 (Abcam, Cambridge, MA); and mouse anti–pan-neurofascin (external epitope, Clone A12/18; University of California, Davis/National Institutes of Health NeuroMab Facility, Bethesda, MD). Rabbit anti-HA and rabbit anti-myc were gifts from A. Sharma (National Institutes of Health). The antibody to p230 was a gift from M. Krieger (MIT, Cambridge, MA). Rabbit anti-GST antiserum and mouse anti-myc clone 9E10 have been described before (Dell’Angelica et al., 1998 (link); Mattera et al., 2011 (link)). Mix-n-stain-CF640R (Biotium, Hayward, CA) was used to label the antibody to neurofascin.
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2

Immunohistochemical analysis of Radixin

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The following primary antibodies were used: rat anti-radixin (R21, gift from S. Tsukita, WB 1:50, ICC 1:50); rabbit anti-radixin (Sigma-Aldrich, #R3653, IHC 1:200); rabbit anti-radixin (Abcam, EP 1862Y, #ab52495, IHC 1:200); mouse anti-γ-adaptin (BD Biosciences, #610386; WB 1:5,000); mouse anti-ezrin (Abcam, #ab4069, clone 3C12, WB 1:1,000); mouse anti-neuN (Millipore, clone A60, #MAB377, IHC 1:1,00). The following secondary antibodies were used: peroxidase-conjugated donkey anti-rabbit (Dianova, Hamburg, Germany, #711-036-152, WB 1:10,000); peroxidase-conjugated donkey anti-rat (Dianova, #712-036-153, WB 1:10,000); peroxidase-conjugated donkey anti-mouse (Dianova, #715-036-151, WB 1:10,000); IRDye 800CW goat anti-rabbit (LI-COR, IgG, #926-32211, WB 1:10,000); IRDye 680RD goat anti-mouse (LI-COR, IgG, #926-68070, WB 1:10,000); Alexa-488 goat anti-mouse (Dianova, #115-545-146, IHC 1:500); Cy3 donkey anti-rabbit (Dianova, #711-166-152, IHC 1:500); Cy3 donkey anti-rat (Dianova, #712-166-150, IHC 1:500); Atto488-labelled FluoTag-X4 anti-rabbit nanobody (NanoTag, IgG, #N2404, IHC 1:200). Alexa-633-coupled phalloidin (Thermo Scientific, #A22284) or Tritc-coupled phalloidin (Tebu-bio, #PHDR1) was used to visualize actin-containing stereocilia. Diamidino-2-phenylindole (DAPI, Sigma, #D9542) was used to stain the nucleus.
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3

Quantification of Neuronal Protein Localization

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Antibodies used were: Rabbit anti-APP C-terminal (1:1000, Cat. No. A8717; Sigma), mouse anti-HA (1:1000, Cat. No. 12CA5;Roche); AP-3 δ3 subunit- mouse- SA4 (1:1000; Developmental Studies Hybridoma Bank); mouse anti-γ-adaptin (Cat No. 610386; BD Bioscience). Secondary antibodies used were donkey anti-mouse HRP (1: 10 000, Cat No. 711–0350150, Jackson Immunoresearch) and goat-anti rabbit HRP (1: 10 000; Biorad). α-tubulin was stained using a mouse monoclonal antibody (Cat No. T5168, Sigma). For immunostaining, donkey anti-rabbit Alexa Fluor 488 (A-11034; Invitrogen) and goat anti-mouse Alex Fluor 546 (A-11003; Invitrogen).
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4

Characterization of Intracellular Trafficking Proteins

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Primary monoclonal antibodies used and their sources (indicated in parentheses) were: mouse anti-TYRP1 (TA99/Mel-5; American Type Culture Collection); mouse anti-γ-Tubulin (GTU-88; Sigma-Aldrich); mouse anti-γ-adaptin (610385; BD); mouse anti-GFP (clones 7.1 and 13.1; Roche); rabbit anti-AP3M1 (ab201227; Abcam); rat anti–mouse LAMP2 (GL2A7; Abcam); rat anti-mouse TfR (CD71; BD 553264); and rat anti-HA (3F10; Roche 11867423001). Primary polyclonal antibodies used and their sources were: rabbit anti-STX13 (a kind gift of Rytis Prekeris, University of Colorado, Denver, CO; Prekeris et al., 1998 (link)); rabbit anti-pallidin (a kind gift of Juan Bonifacino, National Institute of Child Health and Human Development, Bethesda, MD; Moriyama and Bonifacino, 2002 (link)); rabbit anti-PI4KIIIβ (13247-1-AP; Proteintech); rabbit anti-PI4KIIα and anti-PI4KIIβ (kind gifts of Pietro De Camilli, Yale University, New Haven, CT; Guo et al., 2003 (link)); and rabbit anti-GFP (PABG1; Chromotek); Species- and/or mouse isotype–specific secondary antibodies from donkey or goat conjugated to Alexa Fluor 488, Alexa Fluor 594, or Alexa Fluor 640 used for IFM or to Alexa Fluor 680 or Alexa Fluor 790 for immunoblots were obtained from Jackson ImmunoResearch Laboratories.
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5

Antibody Panel for Cellular Protein Localization

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Primary monoclonal antibodies used and their sources (indicated in parentheses) were: mouse anti-TYRP1 (TA99/Mel-5, American Type Culture Collection; Rockville, MD); mouse anti-γ-Tubulin (GTU-88, Sigma); mouse anti-γ-adaptin (BD 610385); mouse anti-GFP (clones 7.1 and 13.1, Roche); rabbit anti-AP3M1 (ab201227; Abcam); rat anti-mouse LAMP2 (GL2A7, Abcam); rat anti-mouse TfR (CD71, BD 553264); and rat anti-HA (3F10, Roche 11867423001). Primary polyclonal antibodies used and their sources were: rabbit anti-STX13 (a kind gift of Rytis Prekeris, Univ. of Colorado, Denver, CO, USA) (Prekeris et al., 1998) ; rabbit anti-pallidin (a kind gift of Juan Bonifacino, National Institute of Child Health and Human Development, Bethesda, MD, USA) (Moriyama and Bonifacino, 2002) ; rabbit anti-PI4KIIIβ (13247-1-AP, Proteintech); rabbit anti-PI4KIIα and anti-PI4KIIβ (kind gifts of Pietro De Camilli, Yale Univ., New Haven, CT, USA) (Guo et al., 2003) ; and rabbit anti-GFP (PABG1, Chromotek); Species-and/or mouse isotype-specific secondary antibodies from donkey or goat conjugated to Alexa Fluor 488, Alexa Fluor 594, or Alexa Fluor 640 used for IFM or to Alexa Fluor 680 or Alexa Fluor 790 for immunoblots were obtained from Jackson ImmunoResearch Laboratories.
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