anti-Huntingtin (HTT) Antikörper

Auf www.antikoerper-online.de finden Sie aktuell 163 Huntingtin (HTT) Antikörper von 20 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen Huntingtin Kits (25) und Huntingtin Proteine (2) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 192 Huntingtin Produkte verfügbar.
Synonyme:
AI256365, C430023I11Rik, CG9995, dhtt, Dmel\\CG9995, Hd, Hdh, Hsap\\HD, htt, huntington, IT15, SLC6A4, ZHD
Alle Antikörper anzeigen Gen GeneID UniProt
HTT 3064 P42858
HTT 15194 P42859
HTT 29424  

Meistgesuchte Reaktivitäten zu anti-Huntingtin (HTT) Antikörper

anti-Human Huntingtin Antikörper:

anti-Mouse (Murine) Huntingtin Antikörper:

anti-Rat (Rattus) Huntingtin Antikörper:

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Weitere Antikörper gegen Huntingtin Interaktionspartner

Zebrafish Huntingtin (HTT) Interaktionspartner

  1. These investigations demonstrate a specific 'rate-limiting' role for huntingtin in formation of the telencephalon and the pre-placodal region, and differing levels of requirement for huntingtin function in specific nerve cell types.

  2. the effects of Htt deficiency in early zebrafish development.

  3. In vivo, huntingtin deficient zebrafish had a severe phenotype and reduced expression of LXR (zeige NR1H3 Antikörper) reg'd genes. An LXR (zeige NR1H3 Antikörper) agonist partially rescued the phenotype and expression of LXR (zeige NR1H3 Antikörper) target genes in huntingtin deficient zebrafish during early development.

Fruit Fly (Drosophila melanogaster) Huntingtin (HTT) Interaktionspartner

  1. Mutant HTT causes severe mislocalization and aggregation of nucleoporins and defective nucleocytoplasmic transport.

  2. Early-onset sleep defects in mutated HTT Drosophila models of Huntington's disease reflect alterations of PKA/CREB signaling.

  3. Htt aggregates cause non-cell-autonomous pathology, including loss of vulnerable neurons that can be prevented by inhibiting endocytosis in these neurons.

  4. Glia regulate steady-state numbers of Htt aggregates expressed in neurons through a clearance mechanism that requires the glial scavenger receptor Draper and downstream phagocytic machinery.

  5. findings support a role for HTT on dynamin 1 (zeige DNM1 Antikörper) function and ER homoeostasis. Proteolysis-induced alteration of this function may be relevant to disease.

  6. Htt modulated histone H3K9 methylation levels at the heterochromatin-euchromatin boundary.

  7. In Drosophila, Huntingtin genetically interacts with autophagy pathway components.

  8. Decreased O-linked GlcNAcylation protects from cytotoxicity mediated by huntingtin exon1 protein fragment

  9. Loss of huntingtin protein results in the disruption of Rab11 vesicle transport.

  10. The specific disruption of Drosophila huntingtin in neuroblast precursors leads to spindle misorientation; Drosophila huntingtin restores spindle misorientation in mammalian cells.

Human Huntingtin (HTT) Interaktionspartner

  1. results suggest that subject-to-subject variation contributes more to variability in N-terminal huntingtin fragments than post mortem delay

  2. We report that endogenous huntingtin protein directly participates in oxidative DNA damage repair. Using novel chromobodies to detect endogenous human huntingtin in live cells, we show that localization of huntingtin to DNA damage sites is dependent on the kinase activity of ataxia telangiectasia mutated (ATM (zeige ATM Antikörper)) protein.

  3. the long HTT 3'UTR (zeige UTS2R Antikörper) suppresses translation.

  4. Soluble oligomers of PolyQ-expanded huntingtin target a multiplicity of key cellular factors.

  5. Peripheral huntingtin silencing does not ameliorate central signs of disease in the B6.HttQ111/+ mouse model of Huntington's disease

  6. The present data emphasize the relevance of expanded CAG RNA to Huntington's disease pathogenesis, indicate that inhibition of HTT expression is not required to reverse motor deficits, and further suggest a therapeutic potential for LNA-CTG in polyglutamine disorders.

  7. Although the mutant huntingtin gene is expressed widely, neurons of the striatum and cortex are selectively affected in Huntington's disease (HD). Our results suggest that this selectivity is attributable to the reduced expression of Foxp1 (zeige FOXP1 Antikörper), a protein expressed selectively in striatal and cortical neurons that plays a neuroprotective role in these cells.

  8. Huntingtin 513 fragment has unique physical interactions with the cellular environment, including, but not limited to, the protein degradation machinery.

  9. The CAG repeat (zeige CELF3 Antikörper) expansion in the exon 1 of the protein huntingtin (HTTex1) that causes the disease leads to the formation of HTT fibrils in vitro and vivo. The fibrils of mutant HTTex1 are able to seed the aggregation of wild type HTTex1 into amyloid fibrils, which in turn can seed the fibril formation of mutant HTTex1.

  10. Mutant HTT causes severe mislocalization and aggregation of nucleoporins and defective nucleocytoplasmic transport.

Mouse (Murine) Huntingtin (HTT) Interaktionspartner

  1. Since the R6/2 mice represent a 'truncated' huntingtin (Htt) mouse model of Huntington's disease (HD), we tested the efficacy of bezafibrate in a 'full-length' Htt mouse model, the BACHD mice. Bezafibrate treatment restored the impaired PPARg (zeige PPARG Antikörper), PPARd (zeige PPARD Antikörper), PGC (zeige PGC Antikörper)-1a signaling pathway, enhanced mitochondrial biogenesis and improved antioxidant defense in the striatum of BACHD mice

  2. treatment of topotecan, a brain-penetrating topoisomerase 1 (zeige TOP1 Antikörper) inhibitor, to HD transgenic mouse considerably improved its motor behavioural abnormalities. Finally, we show that topotecan treatment to HD mouse not only inhibits the expression of transgenic mutant huntingtin, but also at the same time induces the expression of Ube3a (zeige ube3a Antikörper)

  3. Soluble oligomers of PolyQ-expanded huntingtin target a multiplicity of key cellular factors.

  4. The present data emphasize the relevance of expanded CAG RNA to Huntington's disease pathogenesis, indicate that inhibition of HTT expression is not required to reverse motor deficits, and further suggest a therapeutic potential for LNA-CTG in polyglutamine disorders.

  5. Study found that Q175FDN mice exhibited earlier onset and a greater variety and severity of Huntington disease (HD)-like phenotypes as compared to Q175F mice. The characterization of Q175FDN mice suggests this model offers an improved reproduction of HD phenotypes with the mutation in the knocked-in heterozygous state.

  6. Here we show that elimination of Htt expression in the adult mouse results in behavioral deficits, progressive neuropathological changes including bilateral thalamic calcification, and altered brain iron homeostasis.

  7. Although the mutant huntingtin gene is expressed widely, neurons of the striatum and cortex are selectively affected in Huntington's disease (HD). Our results suggest that this selectivity is attributable to the reduced expression of Foxp1 (zeige FOXP1 Antikörper), a protein expressed selectively in striatal and cortical neurons that plays a neuroprotective role in these cells.

  8. Mutant huntingtin markedly accelerates compromised nuclear envelope integrity, impaired nucleocytoplasmic transport, and accumulation of DNA double-strand breaks associated with aging. HTT-linked polyQ initially accumulates in nuclei, leading to disruption of nuclear envelope architecture, partial sequestration of factors essential for nucleocytoplasmic transport (Gle1 (zeige GLE1 Antikörper) and RanGAP1 (zeige RANGAP1 Antikörper)), and intranuclear accumulation of mRNA.

  9. Mutant HTT causes severe mislocalization and aggregation of nucleoporins and defective nucleocytoplasmic transport.

  10. This ability of huntingtin to sense ROS (zeige ROS1 Antikörper) levels at the ER, with phosphorylation and nuclear localization as a response, suggests that ROS (zeige ROS1 Antikörper) stress due to aging could be a critical molecular trigger of huntingtin functions and dysfunctions in HD and may explain the age-onset nature of the disorder.

Huntingtin (HTT) Antigen-Profil

Beschreibung des Gens

Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range in the number of trinucleotide repeats has been identified in normal controls, and repeat numbers in excess of 40 have been described as pathological. The huntingtin locus is large, spanning 180 kb and consisting of 67 exons. The huntingtin gene is widely expressed and is required for normal development. It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widely expressed. The genetic defect leading to Huntington's disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein. One candidate is the huntingtin-associated protein-1, highly expressed in brain, which has increased affinity for huntingtin protein with expanded polyglutamine repeats. This gene contains an upstream open reading frame in the 5' UTR that inhibits expression of the huntingtin gene product through translational repression.

Alternative names and synonyms associated with Huntingtin (HTT)

  • solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 (SLC6A4) Antikörper
  • huntingtin (LOC100216476) Antikörper
  • huntingtin (htt) Antikörper
  • huntingtin (Htt) Antikörper
  • huntingtin (HTT) Antikörper
  • huntingtin (HDH) Antikörper
  • AI256365 Antikörper
  • C430023I11Rik Antikörper
  • CG9995 Antikörper
  • dhtt Antikörper
  • Dmel\\CG9995 Antikörper
  • Hd Antikörper
  • Hdh Antikörper
  • Hsap\\HD Antikörper
  • htt Antikörper
  • huntington Antikörper
  • IT15 Antikörper
  • SLC6A4 Antikörper
  • ZHD Antikörper

Bezeichner auf Proteinebene für anti-Huntingtin (HTT) Antikörper

huntingtin , etID309952.1 , CG9995-PA , CG9995-PB , htt-PA , htt-PB , Huntington's disease protein , huntingtin (Huntington disease) , solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 , Huntington disease , huntingtin-like , huntington disease protein , HD protein homolog , Huntington disease gene homolog , huntington disease protein homolog

GENE ID SPEZIES
100053721 Equus caballus
100216476 Ovis aries
30214 Danio rerio
43392 Drosophila melanogaster
373520 Strongylocentrotus purpuratus
461084 Pan troglodytes
493287 Xenopus (Silurana) tropicalis
700306 Macaca mulatta
100015315 Monodelphis domestica
100145818 Ciona intestinalis
100219938 Taeniopygia guttata
100329031 Saccoglossus kowalevskii
100403524 Callithrix jacchus
100466808 Ailuropoda melanoleuca
3064 Homo sapiens
15194 Mus musculus
29424 Rattus norvegicus
479074 Canis lupus familiaris
397014 Sus scrofa
615059 Bos taurus
100351801 Oryctolagus cuniculus
422878 Gallus gallus
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