Lysyl Oxidase-Like 1 Proteine (LOXL1)

LOXL1 encodes a member of the lysyl oxidase gene family. Zusätzlich bieten wir Ihnen LOXL1 Antikörper (75) und LOXL1 Kits (15) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
LOXL1 4016 Q08397
LOXL1 16949 P97873
LOXL1 315714  
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Showing 10 out of 24 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
Insektenzellen Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 56 Days
7.380,00 €
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Insektenzellen Maus His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 56 Days
7.380,00 €
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HOST_Escherichia coli (E. coli) Maus His tag,T7 tag 100 μg Anmelden zum Anzeigen 13 bis 17 Tage
698,10 €
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HOST_Escherichia coli (E. coli) Ratte His tag,T7 tag 100 μg Anmelden zum Anzeigen 13 bis 17 Tage
728,57 €
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HOST_Escherichia coli (E. coli) Human His tag 100 μg Anmelden zum Anzeigen 13 bis 17 Tage
640,00 €
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HOST_Escherichia coli (E. coli) Human His tag   50 μg Anmelden zum Anzeigen 15 bis 16 Tage
324,76 €
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HOST_Escherichia coli (E. coli) Maus His tag   50 μg Anmelden zum Anzeigen 15 bis 16 Tage
324,76 €
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Hefe Rind (Kuh) His tag   1 mg Anmelden zum Anzeigen 58 bis 70 Tage
3.254,60 €
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Hefe Maus His tag   50 μg Anmelden zum Anzeigen 12 bis 16 Tage
324,76 €
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HOST_Escherichia coli (E. coli) Human Unkonjugiert   5 applications Anmelden zum Anzeigen 5 bis 7 Tage
324,01 €
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LOXL1 Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Human ,

Mouse (Murine) , ,
,
Rat (Rattus)

Weitere Proteine zu Lysyl Oxidase-Like 1 (LOXL1) Interaktionspartnern

Human Lysyl Oxidase-Like 1 (LOXL1) Interaktionspartner

  1. Findings of this current study indicate a different LOXL1 gene expression pattern compared with a recent study that was also performed in the Turkish population.

  2. LOXL1 transcriptional activity was dramatically reduced when a recombinant DNMT3A (zeige DNMT3A Proteine) was concomitantly overexpressed.

  3. The present study, for the first time, shows that the pseudoexfoliation syndrome-associated variant residues in LOXL1 influence processing of the protein, most likely by BMP-1 (zeige BMP1 Proteine).

  4. In this study group of Turkish population, no LOXL1 mutations were found. No associations between the defined SNPs (A320A, R141L and F184F) and the severity of the disease were detected.

  5. Here we show that orthotopic implantation of rat prostate AT-1 tumour cells increased LOX (zeige LOX Proteine) and LOXLs mRNA expressions in the tumour and in the surrounding non-malignant prostate tissue

  6. To identify additional candidate functional variants, we sequenced the entire LOXL1 genomic locus ( approximately 40 kb) in 50 indigenous, black South African XFS (zeige FST Proteine) cases and 50 matched controls.

  7. This is the first study associating two SNPs of LOXL1 (rs3825942 and rs2165241) and XFS (zeige FST Proteine)/XFG in a Spanish population, confirming findings in patients from Europe.

  8. Aortic tissue from Marfan syndrome patients and display enhanced expression of the members of the LOX (zeige LOX Proteine) family, LOX (zeige LOX Proteine) and LOX (zeige LOX Proteine)-like 1.

  9. Our meta-analysis indicates that rs1048661 had weak association with XFG/XFS (zeige FST Proteine); rs3825942 had strongly association with XFG/XFS (zeige FST Proteine); and rs2165241 had significant risk with XFG/XFS (zeige FST Proteine) in some ethnicity.

  10. CTR1 (zeige SLC31A1 Proteine), ATP7A (zeige ATP7A Proteine), and lysyl oxidase (zeige LOX Proteine) were upregulated in the lung tissues and pulmonary arteries of mice with hypoxia-induced pulmonary hypertension and pulmonary arterial smooth muscle cells.

Cow (Bovine) Lysyl Oxidase-Like 1 (LOXL1) Interaktionspartner

Mouse (Murine) Lysyl Oxidase-Like 1 (LOXL1) Interaktionspartner

  1. LOXL1-/- mutant mice develop appendicular and axial skeletal phenotypes characterized by decreased bone volume fraction and compromised trabecular microstructure, predominantly in females

  2. Elimination of LOXL1 in mice impairs the blood-aqueous humor barrier in the ocular anterior segment and causes lens abnormalities consistent with cataract formation, but does not result in deposition of macromolecular material or glaucoma.

  3. There is a possible fundamental role of LOXL-1 in cardiac hypertrophy.

  4. loxl appears non-allelic to rough coat in mice; heart- and skin-specific downregulation of LOXL in rough coat mice, however, may contribute to the extracellular matrix alterations and the rough coat phenotype

  5. Data report that cells in the hippocampal granule cell layer of LOXL -/- mice have significantly smaller somas and muted (zeige MUTED Proteine) long-term potentiation compared to LOXL +/+ mice.

  6. pro-regions of lysyl oxidase (zeige LOX Proteine) and lysyl oxidase-like 1 are required for deposition onto elastic fibers

  7. LOXL1 deficiency caused failure of elastic fiber homeostasis leading to pelvic floor disorders

  8. LOXL1 (lysyl oxidase-like 1) mutation results in a global defect in connective tissues and correlates with altered biomechanical behavior of the vagina and supportive tissues

  9. LOXL1-KO lower urogenital tract anatomical and functional phenotype resembles female pelvic floor dysfunction in humans. Elastin (zeige ELN Proteine) disorganization may lead to such functional abnormalities.

  10. Loxl1(-/-) males bred with control females demonstrated relative fecundity values intermediate between Loxl1(-/-) pairs (lowest fecundity) and control pairs (highest fecundity), suggesting a component of male-factor infertility.

LOXL1 Protein Überblick

Protein Überblick

This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family.

Genbezeichner und Symbole assoziert mit Lysyl Oxidase-Like 1 Proteine (LOXL1)

  • lysyl oxidase-like 1 (LOXL1)
  • lysyl oxidase-like 1 (loxl1)
  • lysyl oxidase-like 1 (Loxl1)
  • lol Protein
  • loxl Protein
  • loxl-1 Protein
  • oxl-1 Protein
  • si:ch211-238c15.1 Protein

Bezeichner auf Proteinebene für Lysyl Oxidase-Like 1 Proteine (LOXL1)

lysyl oxidase-like 1 , lysyl oxidase homolog 1-like , lysyl oxidase homolog 1 , lysyl oxidase-like protein 1 , lysyl oxidase 2

GENE ID SPEZIES
426411 Gallus gallus
706464 Macaca mulatta
100051862 Equus caballus
100124878 Xenopus (Silurana) tropicalis
100388123 Callithrix jacchus
100606325 Nomascus leucogenys
4016 Homo sapiens
281903 Bos taurus
16949 Mus musculus
315714 Rattus norvegicus
560115 Danio rerio
496210 Xenopus laevis
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