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Rabbit Anti-TBCE Antibody (CSB-PA613603ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Tubulin-specific chaperone E Antibody,Tubulin-folding cofactor E Antibody,TBCE AntibodyMore alternative names for the antibody
HRD antibody|KCS antibody|KCS1 antibody|Pac2 antibody|tbce antibody|TBCE_HUMAN antibody|Tubulin specific chaperone e antibody|Tubulin-folding cofactor E antibody|Tubulin-specific chaperone E antibody
Anti-TBCE antibody (ab103006)
Anti-TBCE antibody (ab103006)
Recommended applications: ELISA, WB, IHC
Recommended dilution: User optimized
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Tubulin-specific chaperone E protein (328-527AA)
ELISA, WB, IHC
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Protein function|| |
Tubulin-folding protein; involved in the second step of the tubulin folding pathway and in the regulation of tubulin heterodimer dissociation. Required for correct organization of microtubule cytoskeleton and mitotic splindle, and maintenance of the neuronal microtubule network. .
|Involvement in disease|| |
Hypoparathyroidism-retardation-dysmorphism syndrome (HRDS) [MIM:241410]: An autosomal recessive multisystem disorder characterized by hypoparathyroidism, intrauterine and postnatal growth retardation, psychomotor retardation, epilepsy, microcephaly, and facial dysmorphism. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Kenny-Caffey syndrome 1 (KCS1) [MIM:244460]: An autosomal recessive form of Kenny-Caffey syndrome, a disorder characterized by impaired skeletal development with small and dense bones, short stature, and primary hypoparathyroidism with hypocalcemia. Clinical features include cortical thickening and medullary stenosis of the tubular bones, delayed closure of fontanels, defective dentition, small eyes with hypermetropia, and frontal bossing with a triangular face. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Encephalopathy, progressive, with amyotrophy and optic atrophy (PEAMO) [MIM:617207]: An autosomal recessive, progressive, neurodegenerative encephalopathy with onset in infancy. Affected individuals manifest delayed psychomotor development, severe hypotonia, motor regression, spinal muscular atrophy, distal amyotrophy and weakness of all limbs, and intellectual disability of variable severity. Additional features include optic atrophy, thin corpus callosum, and cerebellar atrophy. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the TBCE family.
|Protein cellular localization|| |
Cytoplasm . Cytoplasm, cytoskeleton .
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CUSABIO BIOTECH CO.
|Product type|| |
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