BCS1-Like (S. Cerevisiae) (BCS1L) ELISA Kits

BCS1L encodes a homolog of the S. Zusätzlich bieten wir Ihnen BCS1-Like (S. Cerevisiae) Antikörper (19) und BCS1-Like (S. Cerevisiae) Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
BCS1L 617 Q9Y276
BCS1L 66821 Q9CZP5
BCS1L    
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Top BCS1-Like (S. Cerevisiae) ELISA Kits auf antikoerper-online.de

Showing 4 out of 5 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Human 1.95 pg/mL 7.8-500 pg/mL Typical standard curve 96 Tests Anmelden zum Anzeigen 15 bis 18 Tage
$910.56
Details
Alle Spezies 2.13 ng/mL 4.94-400 ng/mL 96 Tests Anmelden zum Anzeigen 13 bis 16 Tage
$670.32
Details
Maus 3.75 ng/mL 6.25-400 ng/mL   96 Tests Anmelden zum Anzeigen 13 bis 16 Tage
$436.50
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Ratte 3.75 ng/mL 6.25-400 ng/mL   96 Tests Anmelden zum Anzeigen 13 bis 16 Tage
$436.50
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Am meisten referenzierte BCS1-Like (S. Cerevisiae) ELISA Kits

  1. All Species BCS1L ELISA Kit für Competition ELISA - ABIN437862 : Lim, Teo, Tai, Wong, Ng: Pentosidine levels in nonproteinuric diabetes associated with both low estimated glomerular filtration rate and cataract. in Diabetes, metabolic syndrome and obesity : targets and therapy 2012 (PubMed)
    Show all 3 Pubmed References

Weitere ELISA Kits für BCS1-Like (S. Cerevisiae) Interaktionspartner

Human BCS1-Like (S. Cerevisiae) (BCS1L) Interaktionspartner

  1. We report the first Italian patients with Bjornstad syndrome, two siblings with pili torti and sensorineural hearing loss, in whom we detected two novel compound heterozygous mutations in BCS1L

  2. * Description of a novel homozygous mutation in BCS1L with transient neonatal acidosis and persistent de Toni-Debre-Fanconi-type tubulopathy. * The long survival of patients with phenotypic presentation of severe complex III deficiency is uncommon.

  3. Extensive statistical and cluster analyses revealed a protein profile characteristic for the BCS1L mutant fibroblasts that included alterations in energy metabolism, cell signaling and gene expression regulation, cytoskeleton formation and maintenance.

  4. Exome sequencing revealed novel BCS1L mutations in two siblings with Bjornstad syndrome characterized by hearing loss and hypotrichosis.

  5. A novel behavioral and psychiatric phenotype associated with a p.Gly129Arg BCS1L mutation.

  6. This region encompasses the BCS1L gene.

  7. These results provide new insights into the role of pathogenic BCS1L mutations in mitochondrial function and dynamics.

  8. GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L

  9. a function of BCS1L is to promote the maturation of complex III and the incorporation of the Rieske iron-sulfur protein into the nascent complex. Defective BCS1L leads to the formation of a catalytically inactive, structurally unstable complex III.

  10. assessed whether 232A-->G or other BCS1L mutations were present in infants (n = 21) of Finnish origin with severe, lethal disease compatible with mitochondrial disorder

Mouse (Murine) BCS1-Like (S. Cerevisiae) (BCS1L) Interaktionspartner

  1. COX7A2L (zeige COX7A2L ELISA Kits)/SCAFI and Pre-Complex III Modify Respiratory Chain Supercomplex Formation in Different Mouse Strains with a Bcs1l Mutation.

  2. Studies in the yeast BCS1 ortholog indicate that the Bcs1 protein is anchored in the mitochondrial inner membrane, despite the absence of an N-terminal targeting sequence. Targeting occurs via charged amino acids near the transmembrane domain that act as an internal targeting signal.

  3. Metabolite profiles reveal energy failure and impaired beta-oxidation in liver of mice with complex III deficiency due to a BCS1L mutation.

  4. The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency and is a viable mouse model for mitochondrial hepatopathy.

  5. The predominant expression of BCS1L in the floor plate of the neural tube region, together with its presence in peripheral ganglia from E13 onwards, indicates a role for BCS1L in the development of neural structures.

BCS1-Like (S. Cerevisiae) (BCS1L) Antigen-Profil

Beschreibung des Gens

This gene encodes a homolog of the S. cerevisiae bcs1 protein which is involved in the assembly of complex III of the mitochondrial respiratory chain. The encoded protein does not contain a mitochondrial targeting sequence but experimental studies confirm that it is imported into mitochondria. Mutations in this gene are associated with mitochondrial complex III deficiency and the GRACILE syndrome. Five alternatively spliced transcripts encoding the same protein have been described.

Genbezeichner und Symbole assoziert mit BCS1L

  • mitochondrial chaperone BCS1 (AFUA_3G13000) Antikörper
  • mitochondrial chaperone bcs1 (CC1G_00820) Antikörper
  • mitochondrial chaperone bcs1 (CC1G_00842) Antikörper
  • mitochondrial chaperone BCS1 (CC1G_01181) Antikörper
  • mitochondrial chaperone BCS1 (CC1G_01608) Antikörper
  • mitochondrial chaperone BCS1 (CC1G_11035) Antikörper
  • mitochondrial chaperone BCS1 (CC1G_11036) Antikörper
  • mitochondrial chaperone BCS1 (Bm1_30135) Antikörper
  • mitochondrial ATPase (bcs1lA) Antikörper
  • mitochondrial ATPase (bcs1lB) Antikörper
  • BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone (BCS1L) Antikörper
  • BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone L homeolog (bcs1l.L) Antikörper
  • BCS1-like (yeast) (Bcs1l) Antikörper
  • 9130022O19Rik Antikörper
  • BCS Antikörper
  • BCS1 Antikörper
  • BJS Antikörper
  • DDBDRAFT_0184131 Antikörper
  • DDBDRAFT_0188274 Antikörper
  • DDBDRAFT_0266725 Antikörper
  • DDBDRAFT_0266726 Antikörper
  • DDB_0184131 Antikörper
  • DDB_0188274 Antikörper
  • DDB_0266725 Antikörper
  • DDB_0266726 Antikörper
  • FLNMS Antikörper
  • GRACILE Antikörper
  • h-BCS Antikörper
  • Hs.6719 Antikörper
  • MC3DN1 Antikörper
  • PTD Antikörper

Bezeichner auf Proteinebene für BCS1L

mitochondrial chaperone BCS1 , mitochondrial chaperone bcs1 , BCS1-like protein , h-BCS1 , mitochondrial complex III assembly

GENE ID SPEZIES
3512380 Aspergillus fumigatus Af293
6007738 Coprinopsis cinerea okayama7130
6007764 Coprinopsis cinerea okayama7130
6009613 Coprinopsis cinerea okayama7130
6010435 Coprinopsis cinerea okayama7130
6010570 Coprinopsis cinerea okayama7130
6010571 Coprinopsis cinerea okayama7130
6100920 Brugia malayi
8626976 Dictyostelium discoideum AX4
8628408 Dictyostelium discoideum AX4
617 Homo sapiens
380366 Xenopus laevis
539713 Bos taurus
66821 Mus musculus
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