TFG Monoclonal antibody, PBS Only
TFG Monoclonal Antibody for WB, IHC, Indirect ELISA
Host / Isotype
Mouse / IgG2b
Reactivity
Human, Pig
Applications
WB, IHC, Indirect ELISA
Conjugate
Unconjugated
CloneNo.
1B5B9
Cat no : 66916-1-PBS
Synonyms
Validation Data Gallery
Tested Applications
Recommended dilution
Application | Dilution |
---|---|
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. |
Product Information
66916-1-PBS targets TFG in WB, IHC, Indirect ELISA applications and shows reactivity with Human, Pig samples.
Tested Reactivity | Human, Pig |
Host / Isotype | Mouse / IgG2b |
Class | Monoclonal |
Type | Antibody |
Immunogen | TFG fusion protein Ag27697 相同性解析による交差性が予測される生物種 |
Full Name | TRK-fused gene |
Calculated molecular weight | 400 aa, 43 kDa |
Observed molecular weight | 50-55 kDa |
GenBank accession number | BC023599 |
Gene symbol | TFG |
Gene ID (NCBI) | 10342 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Protein A purification |
Storage Buffer | PBS Only |
Storage Conditions | Store at -80°C. |
Background Information
Protein TFG (TRK-fused gene protein) plays a role in regulating phosphotyrosine-specific phosphatase-1 activity. Mutations in TFG may have important clinical relevance for current therapeutic strategies to treat metastatic melanoma. Defects in TFG are a cause of thyroid papillary carcinoma (TPC), a common tumor of the thyroid that typically arises as an irregular, solid or cystic mass from otherwise normal thyroid tissue. Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is an autosomal-dominant neurodegenerative disorder characterized by widespread fasciculations, proximal-predominant muscle weakness, and atrophy followed by distal sensory involvement. Recent genetic investigation indicates that formation of TFG-containing cytoplasmic inclusions and concomitant mislocalization of TAR DNA-binding protein 43 kDa (TDP-43) underlie motor neuron degeneration in HMSN-P. Pathological overlap of proteinopathies involving TFG and TDP-43 highlights a new pathway leading to motor neuron degeneration.