Biotinidase (BTD) ELISA Kits

Biotinidase functions to recycle biotin in the body by cleaving biocytin (biotin-epsilon-lysine), a normal product of carboxylase degradation, resulting in regeneration of free biotin. Zusätzlich bieten wir Ihnen BTD Antikörper (75) und BTD Proteine (10) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
BTD 686 P43251
BTD 26363 Q8CIF4
BTD 306262 Q5FVF9
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Top BTD ELISA Kits auf antikoerper-online.de

Showing 4 out of 11 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Lieferzeit Preis Details
Human 18.75 37.5 Typical standard curve 96 Tests 15 bis 18 Tage
$910.56
Details
Rind (Kuh)
  96 Tests 2 bis 3 Tage
$867.90
Details
Maus
  96 Tests 15 bis 18 Tage
$875.60
Details
Ratte
  96 Tests 15 bis 18 Tage
$875.60
Details

Weitere ELISA Kits für BTD Interaktionspartner

Fruit Fly (Drosophila melanogaster) Biotinidase (BTD) Interaktionspartner

  1. Conserved seq in mammals, identification of putative gene for biotinidase in Drosophila

Human Biotinidase (BTD) Interaktionspartner

  1. BTD mutation is associated with biotinidase deficiency.

  2. Biotinidase deficiency is reviewed.

  3. Four rare missense variants were identified (ACTBL2 rs73757391 (5q11.2), BTD rs200337373 (3p25.1), KRT13 rs150321809 (17q21.2) and MC2R rs104894658 (18p11.21)), but only MC2R rs104894668 had a large effect size (OR = 9.66).

  4. The history and genetic basis of biotinidase deficiency has been presented. (Review)

  5. 48 novel alterations in the biotinidase gene have been identified; correlating the individual's serum enzymatic activity with genotype, were able to determine the effect of the novel alteration on enzyme activity and, thereby, determine its likelihood of being pathogenic in 44 of these individuals

  6. The common biotinidase gene mutations (p.R157H, p.D444H, c.98-104del7ins3, p.T532M) cumulatively accounted for 72.3% of all the mutant alleles in the Turkish population.

  7. Summary of the demographic features of patients identified as biotinidase deficient from August of 2012 through August of 2013 and mutation analysis results for 20 cases in the southeast region of Turkey.

  8. Three novel pathogenic variants in BTD gene were identified in a cohort of Brazilian patients with biotinidase deficiency and control suggesting an allelic heteregeneity of the condition.

  9. Report incidence of profound biotinase deficiency in Swedish newborns and adoptive immigrant children.

  10. High frequencies of biotinidase mutations may explain the high incidence of biotinidase deficiency in Hungary.

  11. Mutation analysis revealed three novel mutations, c.del631C and c.1557T>G within exon 4 and c.324-325insTA in exon 3 in Biotinidase deficiency patients and families.

  12. Four Somali patients have the P497S mutation, with one of the four being homozygous for the mutation

  13. Six different mutations in the biotinidase gene are identified in biotinidase in four Chinese patients; determination of biotinidase activities are performed for selective screening of biotinidase deficiency

  14. loss of overall biotinidase expression is a novel marker for thyroid cancer aggressiveness.

  15. Plasma BTD activity increases in hepatic glycogen storage disease patients.

  16. 140 known mutations in the biotinidase gene (BTD) that cause biotinidase deficiency, are reported.

  17. Mutations in biotinidase is associated with biotinidase deficiency.

  18. 12 patients with multiple carboxylase deficiency, six mutations were found in the BT gene and 4 in the HLCS gene, including 5 novel mutations.

  19. review of mutations causing biotinidase deficiency

  20. report of 17 novel mutations that cause profound biotinidase deficiency. Six of the mutations are due to deletions, whereas the remaining 11 mutations are missense mutations located throughout the gene

Mouse (Murine) Biotinidase (BTD) Interaktionspartner

  1. Biotinidase knockout mice show cellular energy deficit and altered carbon metabolism gene expression similar to that of nutritional biotin deprivation.

  2. This study demonistrated that biotinidase deficiency mice showed demylination and axonal degeneration.

  3. results indicate low expression of biotinidase throughout the brain, but increased concentrations within the dorsal cochlear nucleus, ventral cochlear nucleus, and superior olivary complex as well as in the hair cells and spiral ganglion of the cochlea

BTD Antigen-Profil

Beschreibung des Gens

Biotinidase functions to recycle biotin in the body by cleaving biocytin (biotin-epsilon-lysine), a normal product of carboxylase degradation, resulting in regeneration of free biotin. Biotinidase has also been shown to have biotinyl-transferase activity. Defects in the biotinidase gene cause multiple carboxylase deficiency.

Genbezeichner und Symbole assoziert mit Biotinidase (BTD) ELISA Kits

  • Biotinidase (Btnd) Antikörper
  • biotinidase (btd) Antikörper
  • biotinidase (BTD) Antikörper
  • biotinidase (Btd) Antikörper
  • Biotinase Antikörper
  • BTD Antikörper
  • CG3599 Antikörper
  • CT12113 Antikörper
  • Dmel\\CG3599 Antikörper
  • zgc:153333 Antikörper

Bezeichner auf Proteinebene für Biotinidase (BTD) ELISA Kits

biotinidase , CG3599-PA , Btd-PA , biotinidase-like , biotinase

GENE ID SPEZIES
31552 Drosophila melanogaster
555376 Danio rerio
677722 Macaca mulatta
100063800 Equus caballus
100226458 Taeniopygia guttata
100409568 Callithrix jacchus
100458389 Pongo abelii
100483327 Ailuropoda melanoleuca
100584490 Nomascus leucogenys
686 Homo sapiens
26363 Mus musculus
306262 Rattus norvegicus
537669 Bos taurus
420639 Gallus gallus
477059 Canis lupus familiaris
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