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SH3 domain and tetratricopeptide repeat-containing protein

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Below are the list of possible SH3 domain and tetratricopeptide repeat-containing protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

SH3 domain and tetratricopeptide repeat-containing protein 1

 SH3 domain and tetratricopeptide repeat-containing protein 1 ELISA Kit
 SH3 domain and tetratricopeptide repeat-containing protein 1 Recombinant
 SH3 domain and tetratricopeptide repeat-containing protein 1 Antibody
SH3TC1:

Chromosomal Location of Human Ortholog: 4p16.1
 SH3TC1 ELISA Kit
 SH3TC1 Recombinant
 SH3TC1 Antibody
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SH3 domain and tetratricopeptide repeat-containing protein 2

 SH3 domain and tetratricopeptide repeat-containing protein 2 ELISA Kit
 SH3 domain and tetratricopeptide repeat-containing protein 2 Recombinant
 SH3 domain and tetratricopeptide repeat-containing protein 2 Antibody
SH3TC2: Defects in SH3TC2 are the cause of Charcot-Marie-Tooth disease type 4C (CMT4C). CMT4C is a recessive form of Charcot-Marie-Tooth disease, the most common inherited disorder of the peripheral nervous system. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathy and primary pe
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ripheral axonal neuropathy. Demyelinating CMT neuropathies are characterized by severely reduced nerve conduction velocities (less than 38 m/sec), segmental demyelination and remyelination with onion bulb formations on nerve biopsy, slowly progressive distal muscle atrophy and weakness, absent deep tendon reflexes, and hollow feet. By convention, autosomal recessive forms of demyelinating Charcot- Marie-Tooth disease are designated CMT4. CMT4C is characterized by onset in childhood, early-onset scoliosis and a distinct Schwann cell pathology. Defects in SH3TC2 are the cause of mononeuropathy of the median nerve mild (MNMN). A disease characterized by median nerve mononeuropathy at the wrist. The clinical presentation ranges from a mild phenotype, consistent with carpal tunnel syndrome, to a severe median nerve mononeuropathy at the wrist associated with evidence of a more widespread axonal polyneuropathy. The latter phenotype is similar to that of patients with hereditary neuropathy with liability to pressure palsies. 4 isoforms of the human protein are produced by alternative splicing.

Cellular Component: cytoplasmic vesicle; plasma membrane; recycling endosome

Molecular Function: protein binding

Biological Process: myelin maintenance in the peripheral nervous system; myelination in the peripheral nervous system; regulation of intracellular protein transport
 Sh3tc2 ELISA Kit
 Sh3tc2 Recombinant
 Sh3tc2 Antibody
 Kiaa1985 ELISA Kit
 Kiaa1985 Recombinant
 Kiaa1985 Antibody
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