Family with Sequence Similarity 3, Member C (FAM3C) Kits ELISA

FAM3C is a member of the family with sequence similarity 3 (FAM3) family and encodes a secreted protein with a GG domain. De plus, nous expédions FAM3C Anticorps (56) et FAM3C Protéines (16) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
FAM3C 10447 Q92520
FAM3C 27999 Q91VU0
Anti-Rat FAM3C FAM3C 312159 Q810F4
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Top FAM3C Kits ELISA sur anticorps-enligne.fr

Showing 2 out of 5 products:

Catalogue No. Reactivité Sensibilité Gamme Images Quantité Fournisseur Livraison Prix Détails
Humain 15.6 pg/mL 62.5-4000 pg/mL Typical standard curve 96 Tests Connectez-vous pour afficher 15 to 18 Days
$910.56
Détails
Souris 3.1 pg/mL 12.5-800 pg/mL Typical standard curve 96 Tests Connectez-vous pour afficher 15 to 18 Days
$910.56
Détails

Plus Kits ELISA pour FAM3C partenaires d'interaction

Human Family with Sequence Similarity 3, Member C (FAM3C) interaction partners

  1. In conclusion, these findings suggested that overexpression of FAM3C in human oral squamous cell carcinoma may predict a poor prognosis for oral squamous cell carcinoma patients.

  2. ILEI contributes to melanoma cell invasiveness in vivo without affecting primary tumor growth and is transcriptionally up-regulated by USF-1.

  3. The ILEI appears to play a crucial role in mediating TGF-beta1-induced EMT through the Akt and ERK pathways, which may provide a therapeutic target for the treatment of fibrotic kidney diseases.

  4. Covalent dimerization of ILEI is associated with breast cancer metastasis.

  5. Data suggest that ILEI does not form interleukin-like four helix-bundle structures; ILEI exists as monomers and as covalent dimers; ILEI dimer exhibits a trans-linked domain swap converting an intramolecular disulfide to an intermolecular disulfide; dimeric ILEI appears to be involved in neoplastic invasiveness.

  6. Results demonstrate that phenotype switching regulates ILEI expression, and that ILEI regulates partial phenotype switching in MITF-low melanoma cell lines.

  7. Ectopic overexpression of UBE4A, but not UBE3C, in cells was downregulated in vitro migration and invasion in these cells. Cumulatively, our data reveals a novel post-translational regulatory mechanism of regulating ILEI1 expression, a protein required for metastatic progression in prostate cancer cells

  8. Study used immunohistochemical staining and biochemical fractionation to examine the regional distribution and subcellular localization of ILEI in mouse brains and in autopsy brains of patients with Alzheimer's disease; results suggest that a decline of ILEI expression may cause accumulation of Abeta in the brain and the eventual development of Alzheimer's disease.

  9. FAM3C expression was dramatically increased in esophageal squamous cell carcinoma and might serve as a valuable prognostic indicator for esophageal squamous cell carcinoma patients after surgery

  10. Altered subcellular ILEI localization strongly correlates with high tumor cell-associated uPAR protein expression.

  11. Our findings indicate that cytoplasmic ILEI expression is a potential marker of EMT and tumour progression in colorectal cancer. ILEI is an independent predictive factor associated with poor prognosis in colorectal cancer.

  12. ILEI could induce, as well as maintain, CD24(low)CD44(high) subpopulation in A549 cells treated with TGF-beta, which might explain its capability to induce metastatic progression.

  13. At the FAM3C gene locus where rs7776725 was located, we identified several other SNPs (rs4727922, rs1803389, rs718766 and rs7793554) that were also associated with BMD.

  14. A cytokine-like protein found in almost all tissues.

  15. ILEI is overexpressed and/or altered in intracellular localization in multiple human tumors.

  16. Data show that FAM3C is decreased in the CSF of temporal lobe epilepsy patients.

Mouse (Murine) Family with Sequence Similarity 3, Member C (FAM3C) interaction partners

  1. ILEI contributes to melanoma cell invasiveness in vivo without affecting primary tumor growth and is transcriptionally up-regulated by USF-1.

  2. Data suggest that Ilei does not form interleukin-like four helix-bundle structures; Ilei exists as monomers and as covalent dimers; Ilei dimer exhibits a trans-linked domain swap converting an intramolecular disulfide to an intermolecular disulfide; dimeric Ilei appears to be involved in neoplastic invasiveness.

  3. overexpression of Fam3c caused reduction of Runx2 expression at both mRNA and protein levels. Fam3c was localized in the cytoplasm and it was not secreted outside the cell during osteoblast differentiation and therefore, may function intracellularly. Furthermore, Fam3c and TGF-beta1 were found to regulate each other reciprocally

  4. In obese diabetic mice, FAM3C expression was reduced in the liver, and hepatic FAM3C restoration improved insulin resistance, hyperglycemia, and fatty liver. FAM3C overexpression increased the expression of heat shock factor 1 (HSF1), calmodulin (CaM), and phosphorylated Akt and reduced that of gluconeogenic and lipogenic genes in diabetic mouse livers with the suppression of gluconeogenesis and lipid deposition.

  5. Study used immunohistochemical staining and biochemical fractionation to examine the regional distribution and subcellular localization of ILEI in mouse brains and in autopsy brains of patients with Alzheimer's disease; results suggest that a decline of ILEI expression may cause accumulation of Abeta in the brain and the eventual development of Alzheimer's disease.

  6. TGF-beta modulates the expression of Dab2 and ILEI mRNA required for epithelial-mesenchymal transdifferentiation by inducing phosphorylation of hnRNP E1, resulting in its release from a structural, 33-nucleotide BAT element in the 3'UTR of Dab2 and ILEI.

  7. FAM3C orthologous protein, may be involved in cell differentiation and proliferation during inner ear embryogenesis

  8. ILEI is overexpressed and/or altered in intracellular localization in multiple human tumors.

  9. ILEI requires cooperation with oncogenic Ras to govern hepatocellular EMT through mechanisms involving PDGF-R/beta-catenin and PDGF-R/Stat3 signaling.

FAM3C profil antigène

Antigen Summary

This gene is a member of the family with sequence similarity 3 (FAM3) family and encodes a secreted protein with a GG domain. A change in expression of this protein has been noted in pancreatic cancer-derived cells.

Gene names and symbols associated with FAM3C

  • family with sequence similarity 3 member C (fam3c) anticorps
  • family with sequence similarity 3 member C (FAM3C) anticorps
  • family with sequence similarity 3, member C (FAM3C) anticorps
  • family with sequence similarity 3, member C (Fam3c) anticorps
  • family with sequence similarity 3, member C (fam3c) anticorps
  • family with sequence similarity 3 member C L homeolog (fam3c.L) anticorps
  • D6Wsu176e anticorps
  • Ilei anticorps
  • wu:fb99h11 anticorps
  • wu:fi35h03 anticorps
  • zgc:55444 anticorps
  • zgc:77090 anticorps

Protein level used designations for FAM3C

hypothetical protein LOC549860 , Protein FAM3C , family with sequence similarity 3, member C , protein FAM3C , interleukin-like EMT inducer , predicted osteoblast protein , FAM3C-like protein

GENE ID SPECIES
549860 Xenopus (Silurana) tropicalis
100221204 Taeniopygia guttata
417758 Gallus gallus
463680 Pan troglodytes
10447 Homo sapiens
612336 Canis lupus familiaris
615690 Bos taurus
27999 Mus musculus
312159 Rattus norvegicus
334205 Danio rerio
443905 Xenopus laevis
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