anti-ATP-Binding Cassette, Sub-Family C (CFTR/MRP), Member 6 (ABCC6) Antikörper

The protein encoded by ABCC6 is a member of the superfamily of ATP-binding cassette (ABC) transporters. Zusätzlich bieten wir Ihnen ABCC6 Kits (20) und ABCC6 Proteine (16) und viele weitere Produktgruppen zu diesem Protein an.

Alle Antikörper anzeigen Gen GeneID UniProt
ABCC6 368 O95255
ABCC6 27421 Q9R1S7
ABCC6 81642 O88269
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Top anti-ABCC6 Antikörper auf antikoerper-online.de

Showing 10 out of 33 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Anbieter Lieferzeit Preis Details
Human Maus Unkonjugiert ELISA, WB Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (36.74 KDa) . Dilution: 1:500~1000 Detection limit for recombinant GST tagged ABCC6 is approximately 0.03ng/ml as a capture antibody. 100 μg Anmelden zum Anzeigen 8 bis 11 Tage
$527.50
Details
Human Ratte Unkonjugiert IHC (fro), IF, WB   1 mL Anmelden zum Anzeigen 6 bis 8 Tage
$544.50
Details
Human Ratte Unkonjugiert IHC (fro), FACS, IF, IHC (p), WB   1 mL Anmelden zum Anzeigen 6 bis 8 Tage
$544.50
Details
Maus Kaninchen Unkonjugiert ICC, IHC, WB Figure. Western Blot; Sample: Recombinant protein. Used in DAB staining on fromalin fixed paraffin- embedded kidney tissue 100 μg Anmelden zum Anzeigen 13 bis 16 Tage
$360.00
Details
Human Maus Unkonjugiert ELISA, WB Detection limit for recombinant GST tagged ABCC6 is approximately 0.03ng/ml as a capture antibody. Western Blot detection against Immunogen (36.74 KDa) . 100 μg Anmelden zum Anzeigen 11 bis 12 Tage
$348.04
Details
Human Ratte Unkonjugiert ICC, IHC, WB   1000 μL Anmelden zum Anzeigen 11 bis 14 Tage
$969.83
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Human Ratte Unkonjugiert ICC, IHC, IHC (fro), WB   1000 μL Anmelden zum Anzeigen 11 bis 14 Tage
$969.83
Details
Human Maus Unkonjugiert ELISA, WB Western Blot detection against Immunogen (37.11 KDa) . 50 μL Anmelden zum Anzeigen 11 bis 12 Tage
$227.50
Details
Human Maus Unkonjugiert WB Western Blot analysis of ABCC6 expression in transfected 293T cell line by ABCC6 MaxPab polyclonal antibody.Lane 1: ABCC6 transfected lysate(10.89 KDa).Lane 2: Non-transfected lysate. 50 μg Anmelden zum Anzeigen 11 bis 12 Tage
$348.04
Details
Human Kaninchen Unkonjugiert WB   100 μL Anmelden zum Anzeigen 16 Days
$366.77
Details

Am meisten referenzierte anti-ABCC6 Antikörper

  1. Human Monoclonal ABCC6 Primary Antibody für FACS, IHC (fro) - ABIN535128 : Bergen, Plomp, Schuurman, Terry, Breuning, Dauwerse, Swart, Kool, van Soest, Baas, ten Brink, de Jong: Mutations in ABCC6 cause pseudoxanthoma elasticum. in Nature genetics 2000 (PubMed)
    Show all 2 Pubmed References

  2. Human Monoclonal ABCC6 Primary Antibody für ELISA, WB - ABIN559916 : Pinckard, Sheehan, Arthur, Schreiber: Constitutive shedding of both p55 and p75 murine TNF receptors in vivo. in Journal of immunology (Baltimore, Md. : 1950) 1997 (PubMed)
    Show all 2 Pubmed References

Weitere Antikörper gegen ABCC6 Interaktionspartner

Human ATP-Binding Cassette, Sub-Family C (CFTR/MRP), Member 6 (ABCC6) Interaktionspartner

  1. Serum levels of MRP8/MRP14 and MRP6 were up-regulated in patients with Graves' disease (GD) and Hashimoto's thyroiditis (HT). In addition, mRNA expression of MRP proteins in PBMCs and the thyroid gland was markedly elevated in these patients.

  2. High URG7 reduces the ER stress by decreasing the amount of unfolded proteins, by increasing both the total protein ubiquitination and the AKT activation and reducing Caspase 3 activation.

  3. Two compound heterozygous ABCC6 loss-of-function mutations, c.4182_4182delG (p.Lys1394Asnfs*9) and c.2900G > A (p.Trp967*), were found

  4. Genetic analysis revealed three nonsense, four frame-shift, one exon deletion and 13 missense mutations in 73 Japanese pseudoxanthoma elasticum patients.

  5. in a French cohort with pseudoxanthoma elasticum, study identified 538 mutational events with 142 distinct variants, of which 66 were novel

  6. ABCC6 overexpression may also contribute to nilotinib and dasatinib resistance in vitro. With nilotinib and dasatinib now front line therapy options in the treatment of CML, concomitant administration of ABCC6 inhibitors may present an attractive option to enhance TKI efficacy

  7. Using an integrated pathway-based approach, we identified polymorphisms in ABCC6, ABCB1 and CYP2C8 associated with overall survival. These associations were replicated in a large independent cohort, highlighting the importance of pharmacokinetic genes as prognostic markers in Ewing sarcoma

  8. ABCC6 knockdown HepG2 cells show: 1) intracellular reductive stress; 2) cell cycle arrest in G1 phase; 3) upregulation of p21Cip p53 independent; and 4) downregulation of lamin A/C. the absence of ABCC6 profoundly changes the HepG2 phenotype, suggesting that Pseudoxanthoma elasticum syndrome is a complex metabolic disease that is not exclusively related to the absence of pyrophosphate in the bloodstream.

  9. ABCC6 deficiency can be rescued by 4-phenylbutyrate therapy in a mouse model expressing human variants

  10. Biochemical and cell biological analyses demonstrate these mutations influence multiple steps in the biosynthetic pathway, minimally altering local domain structure but adversely impacting ABCC6 assembly and trafficking. The differential impacts on local and global protein structure are consistent with hierarchical folding and assembly of ABCC6.

  11. The results suggest that a transmembrane domain is not required for transport function and that a cytosolic loop maintains ABCC6 in a targeting-competent state for the basolateral membrane and might be involved in regulating the nucleotide binding domains.

  12. The results of this study showed that mtDNA(atp6) variants were actively involved in schizophrenia in some families with maternal inheritance of this

  13. Pseudoxanthoma elasticum is due to mutation of the ABCC6 gene on chromosome 16.

  14. Membrane insertion and topology of the amino-terminal domain TMD0 of multidrug-resistance associated protein 6

  15. A direct relationship between reduced ABCC6 levels and the expression of pro-mineralization genes in hepatocytes.

  16. Minimal rescue of the morpholino-induced phenotype was achieved with eight of the nine mutant human ABCC6 mRNAs tested, implying pathogenicity. This study demonstrates that the Chinese PXE population harbors unique ABCC6 mutations.

  17. Virtual screening expands this possibility to explore more compounds that can interact with ABCC6, and may aid in understanding the mechanisms leading to pseudoxanthoma elasticum

  18. The increase in ABCC6 expression accompanied by the induction of cholesterol biosynthesis supposes a functional role for ABCC6 in human lipoprotein and cholesterol homeostasis.

  19. ABCC6 gene is important to determine the genotype of patients diagnosed with pseudoxanthoma elasticum.

  20. Hepatic ABCC6-mediated ATP release is the main source of circulating PPi, revealing an unanticipated role of the liver in systemic PPi homeostasis.

Mouse (Murine) ATP-Binding Cassette, Sub-Family C (CFTR/MRP), Member 6 (ABCC6) Interaktionspartner

  1. abrogated ABCC6 function does cause alterations in the metabolic profile of the liver in accordance with PXE being a metabolic disease originating from liver disturbance

  2. bisphosphonates may be helpful for prevention of mineral deposits in Pseudoxanthoma elasticum and generalized arterial calcification of infancy caused by mutations in the ABCC6 gene.

  3. In a mouse model of CKD, ABCC6 protein expression was decreased in liver and kidney, however mRNA levels were unchanged.

  4. In the Abcc6(-/-) genotype, dermal fibroblasts actively contribute to changes that promote matrix calcification; these cells can be further modulated with time by the calcified environment, contributing to the age-dependent progression.

  5. This study showed that the expression of ABCC6 in liver is an important determinant of calcification in cardiac tissues in response to injuries

  6. Magnesium oxide reduces carotid intima media thickness in Abcc6-/- mouse model for pseudoxanthoma elasticum.

  7. Studied the role of genetic modulation and the role of diet in nephrocalcinosis using two established mouse models of ectopic mineralization, Abcc6(tm1Jfk) and Enpp1(asj) mice.

  8. Report lower elasticity and increased myogenic tone without major changes in agonist-dependent contraction in aged Abcc6(-/-) mouse model of pseudoxanthoma elasticum.

  9. the development of cardiac hypertrophy in the 24-month-old Abcc6(-/-) mice suggests that old pseudoxanthoma elasticum patients might be prone to developing late cardiopathy.

  10. ABCC6 is in the basolateral membrane, mediating the sinusoidal efflux of a metabolite from the hepatocytes to systemic circulation.

  11. A single-nucleotide polymorphism in the Abcc6 gene associates with connective tissue mineralization in mice similar to targeted models for pseudoxanthoma elasticum.

  12. Our finding that ABCC6 localizes to the mitochondria-associated membrane has implications for its mechanism of action in normal and diseased states.

  13. Abcc6 as a novel modulator of cardiac myocyte survival after cardiac ischemia-reperfusion (I/R) injury.

  14. These results show that VK3GS is not the essential metabolite transported by ABCC6 from the liver and preventing the symptoms of pseudoxanthoma elasticum.

  15. genetic and biochemical characterization; contribution to aortic calcification

  16. Upregulation of Abca4 in the liver is a tissue-specific compensatory consequence of the 'knock-out' of Abcc6 in mice.

  17. The level of Abcc6 synthesis was investigated in the liver and kidneys and the phenotype of a beta-thalassemia mouse model (Hbbth3/+) for a period of 14 months.

  18. Abcc6 and Rag1 have roles in ectopic mineralization in a murine model of pseudoxanthoma elasticum

  19. the presence of Abcc6 in elastic tissues is not required for elastic fiber assembly

  20. Targeted ablation of the mouse Abcc6 gene resulted in profound mineralization of skin, arterial blood vessels, and retina.

ABCC6 Antigen-Profil

Protein Überblick

The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). The encoded protein, a member of the MRP subfamily, is involved in multi-drug resistance. Mutations in this gene cause pseudoxanthoma elasticum. Alternatively spliced transcript variants that encode different proteins have been described for this gene.

Genbezeichner und Symbole assoziert mit ABCC6

  • ATP binding cassette subfamily C member 6 (ABCC6) Antikörper
  • ATP-binding cassette, sub-family C (CFTR/MRP), member 6 (Abcc6) Antikörper
  • ATP binding cassette subfamily C member 6 (Abcc6) Antikörper
  • ABC34 Antikörper
  • Abcc1b Antikörper
  • ARA Antikörper
  • DCC Antikörper
  • dyscalc Antikörper
  • Dyscalc1 Antikörper
  • EST349056 Antikörper
  • GACI2 Antikörper
  • MLP1 Antikörper
  • MOAT-E Antikörper
  • MOATE Antikörper
  • Mrp6 Antikörper
  • PXE Antikörper
  • PXE1 Antikörper
  • URG7 Antikörper

Bezeichner auf Proteinebene für ABCC6

ATP-binding cassette sub-family C member 6 , anthracycline resistance-associated protein , multi-specific organic anion transporter E , multidrug resistance-associated protein 6 , ATP-binding cassette, sub-family C, member 6 , multidrug resistance-associated protein-6 , ATP-binding cassette, sub-family C (CFTR/MRP), member 6 , MLP-1 , MRP-like protein 1 , liver multidrug resistance-associated protein 6

GENE ID SPEZIES
368 Homo sapiens
27421 Mus musculus
81642 Rattus norvegicus
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