SH3TC2 rabbit pAb
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SH3TC2 rabbit pAb
Background :
This gene encodes a protein with two N-terminal Src homology 3 (SH3) domains and 10 tetratricopeptide repeat (TPR) motifs, and is a member of a small gene family. The gene product has been proposed to be an adapter or docking molecule. Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C, a childhood-onset neurodegenerative disease characterized by demyelination of motor and sensory neurons. [provided by RefSeq, Jul 2008]Description :
This gene encodes a protein with two N-terminal Src homology 3 (SH3) domains and 10 tetratricopeptide repeat (TPR) motifs, and is a member of a small gene family. The gene product has been proposed to be an adapter or docking molecule. Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C, a childhood-onset neurodegenerative disease characterized by demyelination of motor and sensory neurons. [provided by RefSeq, Jul 2008],UniProt :
Q8TF17Swiss Prot :
Q8TF17Reactivity :
Human; Rat; MouseImmunogen :
The antiserum was produced against synthesized peptide derived from human SH3TC2. AA range:390-430Clonality :
PolyclonalSource :
RabbitApplications :
IHC; IF; ELISAConcentration :
1 mg/mlDilution :
Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.Storage Conditions :
-20°C/1 yearFragment :
IgGSubcellular Location :
Plasma membrane, cytoplasmic vesicle, recycling endosomeOther Product Names :
SH3TC2; KIAA1985; PP12494; SH3 domain and tetratricopeptide repeat-containing protein 2Gene ID (Human) :
79628

