ARG46509

anti-SLITRK6 antibody

anti-SLITRK6 antibody for Western blot,IHC-Formalin-fixed paraffin-embedded sections and Human,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes SLITRK6
Tested Reactivity Hu, Ms, Rat
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name SLITRK6
Antigen Species Human
Immunogen A 13 amino acid synthetic peptide within the last 50 amino acids of human SLITRK6.
Conjugation Un-conjugated
Alternate Names SLIT and NTRK-like family, member 6; Slitrk6; DFNMYP; SLIT and NTRK-like protein 6

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-PAssay-dependent
WBAssay-dependent
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity chromatography purified
Buffer PBS and 0.02% Sodium azide.
Preservative 0.02% Sodium azide
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -559°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 239250 Mouse SLITRK6

GeneID: 84189 Human SLITRK6

Swiss-port # Q8C110 Mouse SLIT and NTRK-like protein 6

Swiss-port # Q9H5Y7 Human SLIT and NTRK-like protein 6

Gene Symbol SLITRK6
Gene Full Name SLIT and NTRK-like family, member 6
Background This gene encodes a member of the SLITRK protein family. Members of this family are integral membrane proteins that are characterized by two N-terminal leucine-rich repeat (LRR) domains and a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing and vision. Mutations in this gene are a cause of myopia and deafness. [provided by RefSeq, Dec 2014]
Function Regulator of neurite outgrowth required for normal hearing and vision. [UniProt]
Cellular Localization Cell membrane. [UniProt]
Calculated MW 95 kDa