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  • KD/KO Validated

TFG Polyclonal antibody

TFG Polyclonal Antibody for WB, IHC, IF/ICC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IHC, IF/ICC, ELISA

Conjugate

Unconjugated

Cat no : 11571-1-AP

Synonyms

TRKT3, TRK-fused gene protein, TRK fused gene protein, TRK fused gene, TF6


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Tested Applications

Positive WB detected inA549 cells, PC-3 cells
Positive IHC detected inhuman gliomas tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF/ICC detected inA549 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:2000
Immunohistochemistry (IHC)IHC : 1:20-1:200
Immunofluorescence (IF)/ICCIF/ICC : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

11571-1-AP targets TFG in WB, IHC, IF/ICC, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivityhuman, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen TFG fusion protein Ag2151 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 numberBC023599
Gene symbol TFG
Gene ID (NCBI) 10342
RRIDAB_2203102
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

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.

Protocols

Product Specific Protocols
WB protocol for TFG antibody 11571-1-APDownload protocol
IHC protocol for TFG antibody 11571-1-APDownload protocol
IF protocol for TFG antibody 11571-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB,IF

Cell Res

A new type of ERGIC-ERES membrane contact mediated by TMED9 and SEC12 is required for autophagosome biogenesis.

Authors - Shulin Li
  • KD Validated
human,mouseWB

Redox Biol

Selenoprotein K contributes to CD36 subcellular trafficking in hepatocytes by accelerating nascent COPII vesicle formation and aggravates hepatic steatosis

Authors - Mengyue You
mouseWB

Neurobiol Dis

Evidence of TRK-Fused Gene (TFG1) function in the ubiquitin-proteasome system.

Authors - Takuya Yagi
  • KD Validated
humanIF

J Med Genet

Novel TFG mutation causes autosomal-dominant spastic paraplegia and defects in autophagy

Authors - Ling Xu
humanIF

Muscle Nerve

Muscle pathology of hereditary motor and sensory neuropathy with proximal dominant involvement with TFG mutation.

Authors - Satoshi Yamashita