Warehouse Overstock Promotion |  Save 10%  on Premium Lab Supplies |  Shop Now

Menu

This product has been added to the cart.

NTRK1 Polyclonal Antibody Store at -20°C

SKU: E-AB-12668-200

  • $ 55995


Request a Quote

NTRK1 Polyclonal Antibody Store at -20°C

 

SKU # E-AB-12668
Reactivity Human, Mouse, Rat
Host Rabbit
Applications IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse, Rat
Applications IHC
Clonality Polyclonal
Immunogen Synthetic peptide of human NTRK1
Abbre NTRK1
Synonyms High affinity nerve growth factor receptor,  High affinity nerve growth factor receptor precursor,  MTC,  NTRK1,  Neurotrophic tyrosine kinase receptor type 1,  Oncogene TRK,  Slow nerve growth,  TRK,  TRK1,  TRK1-tra,  Trk A,  Trk-A,  gp140trk,  p14-TrkA,  p140 TrkA,  p140-TrkA
Swissprot
Cellular Localization Cell membrane. Early endosome membrane. Late endosome membrane. Internalized to endosomes upon binding of NGF or NTF3 and further transported to the cell body via a retrograde axonal transport. Localized at cell membrane and early endosomes before nerve growth factor (NGF) stimulation. Recruited to late endosomes after NGF stimulation. Colocalized with RAPGEF2 at late endosomes (By similarity).
Concentration 0.8 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Neuroscience
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
IHC 1:100-1:300

 

Background

This gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane-bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self-mutilating behavior, mental retardation and cancer. Alternate transcriptional splice variants of this gene have been found, but only three have been characterized to date.