This is a Validated Antibody Database (VAD) review about rat TAG 1, based on 10 published articles (read how Labome selects the articles), using TAG 1 antibody in all methods. It is aimed to help Labome visitors find the most suited TAG 1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
TAG 1 synonym: TAG-1; TAG-564; TAG1; Tax

Knockout validation
R&D Systems
domestic goat polyclonal
  • immunohistochemistry knockout validation; mouse; 1:50; loading ...; fig s1c
R&D Systems TAG 1 antibody (R&D Systems, AF4439) was used in immunohistochemistry knockout validation on mouse samples at 1:50 (fig s1c). Development (2021) ncbi
Developmental Studies Hybridoma Bank
mouse monoclonal (4D7/TAG1)
  • immunohistochemistry knockout validation; mouse; 1:200; loading ...; fig s4c
Developmental Studies Hybridoma Bank TAG 1 antibody (DHSB, 4D7) was used in immunohistochemistry knockout validation on mouse samples at 1:200 (fig s4c). Cell Rep (2020) ncbi
R&D Systems
domestic goat polyclonal
  • immunohistochemistry knockout validation; mouse; 1:50; loading ...; fig s1c
R&D Systems TAG 1 antibody (R&D Systems, AF4439) was used in immunohistochemistry knockout validation on mouse samples at 1:50 (fig s1c). Development (2021) ncbi
Developmental Studies Hybridoma Bank
mouse monoclonal (4D7/TAG1)
  • immunohistochemistry knockout validation; mouse; 1:200; loading ...; fig s4c
Developmental Studies Hybridoma Bank TAG 1 antibody (DHSB, 4D7) was used in immunohistochemistry knockout validation on mouse samples at 1:200 (fig s4c). Cell Rep (2020) ncbi
mouse monoclonal (3.1C12)
  • immunohistochemistry; fruit fly ; loading ...; fig s1r
Developmental Studies Hybridoma Bank TAG 1 antibody (DSHB, 3.1C12) was used in immunohistochemistry on fruit fly samples (fig s1r). Cell Rep (2019) ncbi
mouse monoclonal (4D7/TAG1)
  • immunocytochemistry; mouse; 1:100; loading ...; fig 4l
  • immunohistochemistry; mouse; 1:100; loading ...; fig 4h
Developmental Studies Hybridoma Bank TAG 1 antibody (DSHB, 4D7/TAG1-C) was used in immunocytochemistry on mouse samples at 1:100 (fig 4l) and in immunohistochemistry on mouse samples at 1:100 (fig 4h). Cell Rep (2019) ncbi
mouse monoclonal (4D7/TAG1)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 1 - s2b
Developmental Studies Hybridoma Bank TAG 1 antibody (DSHB, 4D7/TAG1) was used in immunohistochemistry - frozen section on mouse samples (fig 1 - s2b). elife (2018) ncbi
mouse monoclonal (4D7/TAG1)
  • immunohistochemistry; mouse; 1:100; loading ...; tbl 1
In order to research the expression of Nogo-B at the floor plate and its function, Developmental Studies Hybridoma Bank TAG 1 antibody (DSHB, 4D7/TAG1) was used in immunohistochemistry on mouse samples at 1:100 (tbl 1). J Comp Neurol (2017) ncbi
mouse monoclonal (3.1C12)
  • immunohistochemistry - frozen section; mouse; fig s4i
Developmental Studies Hybridoma Bank TAG 1 antibody (DSHB, 3.1C12) was used in immunohistochemistry - frozen section on mouse samples (fig s4i). Science (2015) ncbi
mouse monoclonal (4D7/TAG1)
  • immunohistochemistry - frozen section; mouse
Developmental Studies Hybridoma Bank TAG 1 antibody (DSHB, 4D7) was used in immunohistochemistry - frozen section on mouse samples . Acta Neuropathol Commun (2013) ncbi
mouse monoclonal (4D7/TAG1)
  • immunohistochemistry - free floating section; mouse; 1:40
In order to examine the functions of Smad proteins during cerebellum development, Developmental Studies Hybridoma Bank TAG 1 antibody (Hybridoma bank, 4D7) was used in immunohistochemistry - free floating section on mouse samples at 1:40. Mol Cell Biol (2013) ncbi
mouse monoclonal (4D7/TAG1)
  • immunohistochemistry - frozen section; mouse
In order to exmaine the role of Cdk5 in the neurnal migration in the developing spinal cord, Developmental Studies Hybridoma Bank TAG 1 antibody (Developmental Studies Hybridoma Bank, 4D7) was used in immunohistochemistry - frozen section on mouse samples . J Comp Neurol (2007) ncbi
Articles Reviewed
  1. Delgado C, Bu L, Zhang J, Liu F, Sall J, Liang F, et al. Neural cell adhesion molecule is required for ventricular conduction system development. Development. 2021;148: pubmed publisher
  2. Suter T, Blagburn S, Fisher S, Anderson Keightly H, D Elia K, Jaworski A. TAG-1 Multifunctionality Coordinates Neuronal Migration, Axon Guidance, and Fasciculation. Cell Rep. 2020;30:1164-1177.e7 pubmed publisher
  3. Lim H, Bao H, Liu Y, Wang W. Select Septate Junction Proteins Direct ROS-Mediated Paracrine Regulation of Drosophila Cardiac Function. Cell Rep. 2019;28:1455-1470.e4 pubmed publisher
  4. Gorla M, Santiago C, Chaudhari K, Layman A, Oliver P, Bashaw G. Ndfip Proteins Target Robo Receptors for Degradation and Allow Commissural Axons to Cross the Midline in the Developing Spinal Cord. Cell Rep. 2019;26:3298-3312.e4 pubmed publisher
  5. Baba K, Yoshida W, Toriyama M, Shimada T, Manning C, Saito M, et al. Gradient-reading and mechano-effector machinery for netrin-1-induced axon guidance. elife. 2018;7: pubmed publisher
  6. Wang L, Yu C, Wang J, Leung P, Ma D, Zhao H, et al. Nogo-B is the major form of Nogo at the floor plate and likely mediates crossing of commissural axons in the mouse spinal cord. J Comp Neurol. 2017;525:2915-2928 pubmed publisher
  7. Amin N, Bai G, Klug J, Bonanomi D, Pankratz M, Gifford W, et al. Loss of motoneuron-specific microRNA-218 causes systemic neuromuscular failure. Science. 2015;350:1525-9 pubmed publisher
  8. Nguyen H, Ostendorf A, Satz J, Westra S, Ross Barta S, Campbell K, et al. Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteins. Acta Neuropathol Commun. 2013;1:58 pubmed publisher
  9. Tong K, Kwan K. Common partner Smad-independent canonical bone morphogenetic protein signaling in the specification process of the anterior rhombic lip during cerebellum development. Mol Cell Biol. 2013;33:1925-37 pubmed publisher
  10. Yip Y, Capriotti C, Drill E, Tsai L, Yip J. Cdk5 selectively affects the migration of different populations of neurons in the developing spinal cord. J Comp Neurol. 2007;503:297-307 pubmed