Interferon Induced Transmembrane Protein 5 Proteine (IFITM5)

Plays a role in bone mineralization (By similarity).. Zusätzlich bieten wir Ihnen IFITM5 Antikörper (37) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
Ratte IFITM5 IFITM5 293617  
IFITM5 387733 A6NNB3
IFITM5 73835 O88728
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Showing 3 out of 3 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Lieferzeit Preis Details
Insektenzellen Maus rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg 50 bis 55 Tage
$5,262.31
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Insektenzellen Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg 50 bis 55 Tage
$7,493.38
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HEK-293 Cells Human Myc-DYKDDDDK Tag Validation with Western Blot 20 μg 11 Days
$888.80
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IFITM5 Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Human ,
,
Mouse (Murine)

Weitere Proteine zu Interferon Induced Transmembrane Protein 5 (IFITM5) Interaktionspartnern

Human Interferon Induced Transmembrane Protein 5 (IFITM5) Interaktionspartner

  1. Two mutations in IFITM5 causing distinct forms of osteogenesis imperfect.

  2. The point mutation, c.-14C>T in the 5'-untranslated region of IFITM5, is responsible for osteogenesis imperfecta type V in Chinese patients.

  3. The IFITM5 5' UTR was sequenced in 9 heterozygous subjects with osteogenesis imperfecta type V. Both wild-type and mutant IFITM5 mRNA transcripts were present in bone. Identical mutations have variable phenotypic expression, even within the same family.

  4. The bone mineral density varied greatly, even within families. Our study thus highlights the phenotypic variability of OI type V caused by the IFITM5 mutation.

  5. Recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V.

  6. IFITM5 mutation is associated with Osteogenesis imperfecta type V.

  7. study demonstrates the presence of a recurrent IFITM5 mutation in a population of patients with osteogenesis imperfecta type V; even though the disease-causing mutation is identical among patients, the interindividual phenotypic variability is considerable

  8. A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V.

  9. A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.

Mouse (Murine) Interferon Induced Transmembrane Protein 5 (IFITM5) Interaktionspartner

  1. IFITM5 was expressed in the dental follicle and the developing alveolar bone

  2. results suggest that expression of mutant IFITM5 causes abnormal skeletal development, low bone mass, and abnormal osteoblast differentiation

  3. The purpose of the current study was to re-assess the topology, localization, and biochemical properties of BRIL and compare it to the osteogenesis imperfecta type V mutant in MC3T3 osteoblasts.

  4. These results indicate that the S-palmitoylation on IFITM5 promotes the interaction with FKBP11.

  5. Key roles for the Sp members and GLI2 that possibly cooperate to activate Bril when the promoter becomes demethylated.

  6. Natural antisense transcripts enhance bone formation by increasing sense IFITM5 transcription.

  7. Ifitm5 deficiency might have a greater effect on prenatal bone development.

  8. these results suggest that IFITM5 is involved not only in bone formation, but also in immune system activity.

  9. Bril is a novel osteoblast protein and showed a role in mineralization, possibly identifying a new regulatory pathway in bone formation.

IFITM5 Protein Überblick

Protein Überblick

Plays a role in bone mineralization (By similarity).

Genbezeichner und Symbole assoziert mit IFITM5

  • interferon induced transmembrane protein 5 (Ifitm5)
  • interferon induced transmembrane protein 5 (IFITM5)
  • interferon-induced transmembrane protein 1 (LOC606890)
  • 1110003J06Rik Protein
  • AW213665 Protein
  • Bril Protein
  • DSPA1 Protein
  • fragilis4 Protein
  • Hrmp1 Protein
  • Hrtm1 Protein
  • OI5 Protein

Bezeichner auf Proteinebene für IFITM5

interferon-induced transmembrane protein 5 , interferon induced transmembrane protein 5 , bone-restricted ifitm-like protein , bone-restricted interferon-induced transmembrane protein-like protein , dispanin subfamily A member 1 , bone-restricted interferon induced transmembrane protein-like protein , fragilis family member 4 , fragilis4 , haemopoiesis related membrane protein 1

GENE ID SPEZIES
293617 Rattus norvegicus
422992 Gallus gallus
450915 Pan troglodytes
526461 Bos taurus
606890 Canis lupus familiaris
697314 Macaca mulatta
387733 Homo sapiens
73835 Mus musculus
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