Product Description

FEV Rabbit Polyclonal Antibody

Sizes: 50μL, 100μL

Catalogue Numbers: ES6674-50, ES6674-100

Lead times: 1-2 weeks, if manufacturer has product in stock

Manufacturer/Ship Location: China

Background: This gene belongs to the ETS transcription factor family. ETS family members have a highly conserved 85-amino acid ETS domain that binds purine-rich DNA sequences. The alanine-rich C-terminus of this gene indicates that it may act as a transcription repressor. This gene is exclusively expressed in neurons of the central serotonin (5-HT) system, a system implicated in the pathogeny of such psychiatric diseases as depression, anxiety, and eating disorders. In some types of Ewing tumors, this gene is fused to the Ewing sarcoma (EWS) gene following chromosome translocations. [provided by RefSeq, Jul 2008],

Reactivity: Human, Rat, Mouse,

Host: Rabbit

Applications: WB, ELISA

Alternate Names: FEV, PET1, Protein FEV, Fifth Ewing variant protein, PC12 ETS domain-containing transcription factor 1, PC12 ETS factor 1, Pet-1

Clonality: Polyclonal

Immunogen: Synthesized peptide derived from the N-terminal region of human FEV.

Isotype: IgG

Target: FEV

Specificity: FEV Polyclonal Antibody detects endogenous levels of FEV protein.

Dilution: Western Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml,

Formlation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Expression: In brain, exclusively expressed in the major serotonergic neurons of the dorsal and median raphe nuclei located in the midbrain and pons, Also detected in prostate and small intestine,

Observed Band (KD): 25kD

Fields: Transcriptional misregulation in cancer

Function: Disease: A chromosomal translocation involving FEV is found in Ewing tumors. Translocation t(2, 21, 22)(q23, q22, q12) that forms a EWSR1-FEV fusion protein with a potential oncogenic activity
Disease: Genetic variation in FEV may be associated with susceptibility to sudden infant death syndrome (SIDS) [MIM: 272120]. SIDS remains elusive in its causes and devastating in its consequences. Despite the impressive decline in the incidence of SIDS since the recommendation to avoid the prone sleep position, SIDS remains a leading cause of death in the first year of life
Function: Functions as a transcriptional regulator. According to PubMed: 1761502 it functions as a transcriptional repressor. Functions in the differentiation and the maintenance of the central serotonergic neurons. May play a role in cell growth
Similarity: Belongs to the ETS family
Similarity: Contains 1 ETS DNA-binding domain
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Subcellular Location: Nucleus

Storage and Stability: -20°C/1 year

Gene Name: FEV

Protein Name: Protein FEV

Mouse SwissProt Number: Q8QZW2

Research Use Only