anti-Biotinidase (BTD) Antibodies

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. Additionally we are shipping BTD Proteins (10) and BTD Kits (8) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
BTD 686 P43251
BTD 26363 Q8CIF4
BTD 306262 Q5FVF9
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Top anti-BTD Antibodies at antibodies-online.com

Showing 10 out of 76 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Delivery Price Details
Human Goat Un-conjugated ELISA, WB   100 μg 6 to 7 Days
$429.87
Details
Human Rabbit Un-conjugated IHC (p), WB WB Image Sample (30 ug of whole cell lysate) A: Jurkat 7.5% SDS PAGE antibody diluted at 1:1000 IHC-P Image BTD antibody [N3C3] detects BTD protein at cytosol on mouse hind brain by immunohistochemical analysis. Sample: Paraffin-embedded mouse hind brain. BTD antibody [N3C3] , dilution: 1:250. 100 μL 3 to 4 Days
$466.18
Details
Human Rabbit Un-conjugated IHC, WB Western blot analysis of extracts of various cell lines, using BTD antibody (ABIN5973709) at 1/1000 dilution. Immunohistochemistry of paraffin-embedded rat brain using BTD antibody (ABIN5973709) at dilution of 1/100 (40x lens). 100 μL 11 to 16 Days
$422.09
Details
Human Rabbit Un-conjugated IHC, WB Immunohistochemistry of paraffin-embedded human prostate using BTD antibody at dilution of 1:100 (40x lens). 100 μL 11 to 13 Days
$363.06
Details
Human Goat Un-conjugated WB Staining of Human Liver lysate using Biotinidase antibody at 0.5 µg/ml (35µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence. 0.1 mg 6 to 8 Days
$440.00
Details
Human Rabbit Un-conjugated ICC, IHC, WB Western Blot; Sample: Human Urine; Primary Ab: 1µg/ml Rabbit Anti-Human BTD Antibody Second Ab: 0.2µg/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody (Catalog: SAA544Rb19) Figure. Western Blot; Sample: Recombinant protein. 100 μL 13 to 16 Days
$245.00
Details
Human Rabbit Un-conjugated IHC (p), ELISA, WB Human Biotinidase / biotinase / BTD Immunohistochemistry(IHC) 7844 Human Biotinidase / biotinase / BTD Immunohistochemistry(IHC) 7845 100 μL 14 to 16 Days
$247.82
Details
Human Mouse Un-conjugated WB Western Blot analysis of BTD expression in transfected 293T cell line by BTD MaxPab polyclonal antibody.Lane 1: BTD transfected lysate(59.73 KDa).Lane 2: Non-transfected lysate. 50 μL 11 to 12 Days
$364.00
Details
Human Rabbit Un-conjugated WB Western blot analysis of extracts of various cell lines, using BTD antibody (ABIN6290108) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 90s. 50 μL 11 to 13 Days
$305.01
Details
Human Goat Biotin ELISA, WB   100 μg 11 to 14 Days
$610.50
Details

Top referenced anti-BTD Antibodies

  1. Human Polyclonal BTD Primary Antibody for ELISA, WB - ABIN4256282 : Cowan, Blitzer, Wolf: Technical standards and guidelines for the diagnosis of biotinidase deficiency. in Genetics in medicine : official journal of the American College of Medical Genetics 2010 (PubMed)

More Antibodies against BTD Interaction Partners

Fruit Fly (Drosophila melanogaster) Biotinidase (BTD) interaction partners

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

Human Biotinidase (BTD) interaction partners

  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) interaction partners

  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 Profile

Protein Summary

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.

Gene names and symbols associated with anti-Biotinidase (BTD) Antibodies

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

Protein level used designations for anti-Biotinidase (BTD) Antibodies

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

GENE ID SPECIES
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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