Tocopherol (Alpha) Transfer Protein (TTPA) ELISA Kits

TTPA encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. Zusätzlich bieten wir Ihnen TTPA Antikörper (29) und TTPA Proteine (6) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
TTPA 7274 P49638
TTPA 25571 P41034
TTPA 50500 Q8BWP5
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Top TTPA ELISA Kits auf

Showing 5 out of 14 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Maus 0.055 ng/mL 0.15 ng/mL - 10 ng/mL 96 Tests Anmelden zum Anzeigen 13 bis 16 Tage
Human 0.054 ng/mL 0.156-10 ng/mL   96 Tests Anmelden zum Anzeigen 2 bis 3 Tage
Human 25.3 pg/mL 62.5 pg/mL - 4000 pg/mL   96 Tests Anmelden zum Anzeigen 15 bis 17 Tage
Ratte 0049 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Anmelden zum Anzeigen 15 bis 17 Tage
  96 Tests Anmelden zum Anzeigen 15 bis 18 Tage

Weitere ELISA Kits für TTPA Interaktionspartner

Human Tocopherol (Alpha) Transfer Protein (TTPA) Interaktionspartner

  1. These findings provide the basis for a proposed mechanistic model that describes TTP (zeige ADAMTS13 ELISA Kits)-facilitated trafficking of alpha-tocopherol through hepatocytes.

  2. Single-nucleotide polymorphisms that are commonly found in healthy humans dramatically affect promoter activity of the TTPA gene.

  3. The crystal structure of the alpha-TTP-phosphatidylinositol phosphates (PIPs (zeige GPRASP1 ELISA Kits)) complex revealed that the familial vitamin E deficiency-related arginine residues interacted with phosphate groups of the PIPs (zeige GPRASP1 ELISA Kits) and that the PIPs (zeige GPRASP1 ELISA Kits) binding caused the lid of the alpha-tocopherol-binding pocket to open.

  4. Data show that reduction ("knockdown") of tocopherol transfer protein (TTP (zeige ADAMTS13 ELISA Kits)) expression resulted in resistance to the vitamin E.

  5. Substitution of residues in helices A8 (F165A and F169A) and A10 (I202A, V206A and M209A) decreased the rate of intermembrane ligand transfer as well as protein adsorption to phospholipid bilayers.

  6. First case of a mutated form of the TTPA gene in a patient also carrying a spinocerebellar ataxia type 8 expansion.

  7. the positively charged surface of TTPA may serve to orient an interacting protein, which might function to regulate the release of alpha-T through an induced change in conformation of ATTP

  8. Findings suggest the possibility that ataxia with vitamin E deficiency syndrome (AVED) may not arise from an inability of TTP (zeige ADAMTS13 ELISA Kits) to bind or to transfer alpha tocopherol, but rather from defects in other activities of the protein.

  9. Nuclear localization of TTPA in in trophoblast, fetal capillaries' endothelium and amnion epithelium of human term placentamay represent a novel function of TTPA

  10. In Ataxia with vitamin E deficiency two TTPA mutations were identified: a truncating mutation in a homozygous patient, and a Gly246Arg missense mutation in a compound heterozygous patient associated with a mild and slowly progressive form of the disease.

Mouse (Murine) Tocopherol (Alpha) Transfer Protein (TTPA) Interaktionspartner

  1. Results suggest that lipid peroxidation due to depletion of alpha-tocopherol impairs Abeta (zeige APP ELISA Kits) clearances from the brain and from the blood, possibly causing increased Abeta (zeige APP ELISA Kits) accumulation in Ttpa(-/-)APPsw brain and plasma.

  2. Endogenous TTPA, through the enhancement of MMP 9 (zeige MMP9 ELISA Kits) expression and proteolytic activation, plays an essential role in the pathogenesis of heparin-produced cerebral hemorrhage.

  3. TTP (zeige ZFP36 ELISA Kits) transports alpha-TCP and oral administration of TTP (zeige ZFP36 ELISA Kits) compensates for TTP (zeige ZFP36 ELISA Kits) in TTP (zeige ZFP36 ELISA Kits)-deficient mice

  4. These data suggest that in vivo network of alpha-tocopherol (AT), AT-metabolites and ATTP affects the transcription of genes driven by AhR (zeige AHR ELISA Kits), Nrf2 (zeige NFE2L2 ELISA Kits) and NF-kappaB (zeige NFKB1 ELISA Kits), transcription factor networks.

  5. p75(NTR (zeige NGFR ELISA Kits))is up-regulated after tissue injury, blocks fibrinolysis by down-regulating the serine protease (zeige F2 ELISA Kits), tissue plasminogen activator (zeige PLAT ELISA Kits), and up-regulating PAI-1 (zeige SERPINE1 ELISA Kits).

  6. changes in hepatic TTP (zeige ZFP36 ELISA Kits) concentrations were minimal in response to dietary vitamin E levels or environmental tobacco smoke-related oxidative stress

  7. Increase expression of tPA implicate fibrinolysis in ALD progression.

TTPA Antigen-Profil

Beschreibung des Gens

This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa.

Genbezeichner und Symbole assoziert mit TTPA

  • alpha tocopherol transfer protein (TTPA) Antikörper
  • tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency) (ttpa) Antikörper
  • alpha tocopherol transfer protein (Ttpa) Antikörper
  • tocopherol (alpha) transfer protein (Ttpa) Antikörper
  • alpha-TTP Antikörper
  • alphaTTP Antikörper
  • ATTP Antikörper
  • AVED Antikörper
  • TTP Antikörper
  • TTP1 Antikörper

Bezeichner auf Proteinebene für TTPA

alpha-tocopherol transfer protein , tocopherol (alpha) transfer protein , alpha-TTP , tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency) , Alpha-tocopherol transfer protein , Tocopherol transfer protein alpha , alpha TTP

286813 Bos taurus
403627 Canis lupus familiaris
472778 Pan troglodytes
771074 Gallus gallus
100196332 Salmo salar
100526668 Ovis aries
7274 Homo sapiens
25571 Rattus norvegicus
50500 Mus musculus
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