anti-Ceroid-Lipofuscinosis, Neuronal 3 (CLN3) Antikörper

CLN3 encodes a protein that is involved in lysosomal function. Zusätzlich bieten wir Ihnen CLN3 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.

Alle Antikörper anzeigen Gen GeneID UniProt
CLN3 1201 Q13286
CLN3 12752 Q61124
CLN3 293485  
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Top anti-CLN3 Antikörper auf antikoerper-online.de

Showing 10 out of 38 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Anbieter Lieferzeit Preis Details
Human Maus Unkonjugiert WB Western Blot analysis of CLN3 expression in transfected 293T cell line by CLN3 monoclonal antibody (M03), clone 1G10. Lane 1: CLN3 transfected lysate(47.623 KDa). Lane 2: Non-transfected lysate. 0.1 mg Anmelden zum Anzeigen 8 bis 11 Tage
$450.00
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Human Kaninchen Unkonjugiert IHC, WB 100 μL Anmelden zum Anzeigen 16 Days
$334.02
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Human Kaninchen Alexa Fluor 555 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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Human Kaninchen Alexa Fluor 350 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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Human Kaninchen Alexa Fluor 647 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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Human Kaninchen Cy7 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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Human Kaninchen HRP IHC (p), WB   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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Human Kaninchen Alexa Fluor 488 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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Human Kaninchen Cy3 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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Human Kaninchen Cy5 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 21 Tage
$405.90
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CLN3 Antikörper nach Reaktivität, Anwendung, Klonalität and Konjugat

Attribute Applikationen Wirt Klonalität Konjugat
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Weitere Antikörper gegen CLN3 Interaktionspartner

Human Ceroid-Lipofuscinosis, Neuronal 3 (CLN3) Interaktionspartner

  1. AAV2-CLN3 was efficacious in restoring full-length CLN3 transcript and protein in patient-specific fibroblasts and iPSC-derived retinal neurons. When injected into the subretinal space of wild-type mice, purified AAV2-CLN3 did not show any evidence of retinal toxicity

  2. The lysosomal enzyme cathepsin D (CTSD (zeige CTSD Antikörper)) mediates the proteolytic cleavage of PSAP (zeige PSAP Antikörper) precursor into saposins A-D. Myc (zeige MYC Antikörper)-CLN3 colocalized with CTSD (zeige CTSD Antikörper) and activity of CTSD (zeige CTSD Antikörper) decreased as myc (zeige MYC Antikörper)-CLN3 expression increased, and clearly decreased under hyperosmotic conditions

  3. This is the first detailed morphological evaluation of CLN3 patients in the first years after the subjective onset of ocular symptoms. CLN3 is characterized by an early degeneration predominant of the first and second neuron compared to other macular and generalized retinal dystrophies.

  4. The age at onset and natural progression of retinal disease differs greatly between syndromic and nonsyndromic CLN3 disease, which may be associated with genotypic differences.

  5. CLN3 knockdown inhibits cell proliferation and induces G0/G1 cell cycle arrest in the A2780 cell line and its drug-resistant sub-lines.

  6. The membrane topology of human CLN3 protein.

  7. The eyes and vision of heterozygous carriers of CLN3 disease showed normal features when compared to a control group, which controverts a previously suggested retinal dysfunction in these subjects.

  8. This new model system, which allows for the study of Cln3 function in both single cells and a multicellular organism, together with the observation that expression of human CLN3 restores abnormalities in Dictyostelium cln3- cells

  9. These results further support an important role for the CLN3 protein in intracellular Ca(2 (zeige CA2 Antikörper)+) handling and in autophagic pathway flux and establish a powerful new platform for therapeutic screening.

  10. CLN3 mutation is associated with neuronal ceroid lipofuscinosis (zeige CLN6 Antikörper).

Mouse (Murine) Ceroid-Lipofuscinosis, Neuronal 3 (CLN3) Interaktionspartner

  1. Our subcellular localization study in neurons refines the localization and subcellular targeting of CLN3 to late endosomal-lysosomal compartments

  2. findings in two distinct lysosome-related degradative pathways constitute the first description of a deficit in the retinal pigment epithelium caused by loss of CLN3

  3. The small GTPase (zeige RACGAP1 Antikörper) Cdc42 (zeige CDC42 Antikörper) is misregulated in the absence of CLN3, and thus may be a common link to multiple cellular defects.

  4. Rssults suggested that CLN2 (zeige TPP1 Antikörper), CLN3 and CLN5 (zeige CLN5 Antikörper) genes may play an important role in early embryonal neurogenesis.

  5. The aim of our study was to investigate the visual disease progression in the Cln3 (Deltaex7/8) mice.

  6. CLN3 facilitates transport of microdomain-associated proteins.

  7. results demonstrate altered glutamate (zeige GRIN1 Antikörper) receptor function in Cln3(Deltaex7/8) neurons and suggest that both AMPA (zeige GRIA3 Antikörper) and NMDA receptors are potential therapeutic targets in juvenile neuronal ceroid lipofuscinosis (zeige CLN6 Antikörper)

  8. The migration defect in Cln3(-/-) results, in part, from the loss of the CLN3-myosin-IIB (zeige MYH10 Antikörper) interaction.

  9. Findings suggest an osmoregulated role for CLN3p in renal medullary control of water and K(+) balance.

  10. Cln3(Deltaex7/8) knock-in mice with the common juvenile-onset neuronal ceroid lipofuscinosis (zeige CLN6 Antikörper) (JNCL; Batten disease) mutation exhibit progressive neurologic disease that begins before birth.

Cow (Bovine) Ceroid-Lipofuscinosis, Neuronal 3 (CLN3) Interaktionspartner

  1. The candidate genes for bovine Neuronal Ceroid Lipofuscinosis (zeige CLN6 Antikörper), CLN3, CLN5 (zeige CLN5 Antikörper) and CLN6 (zeige CLN6 Antikörper), have been mapped to facilitate linkage analysis in cattle and sheep.

CLN3 Antigen-Profil

Protein Überblick

This gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene.

Genbezeichner und Symbole assoziert mit CLN3

  • CLN3, battenin (CLN3) Antikörper
  • ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease) (Cln3) Antikörper
  • ceroid-lipofuscinosis, neuronal 3 (cln3) Antikörper
  • battenin (PTRG_05620) Antikörper
  • CLN3, battenin (Cln3) Antikörper
  • battenin (LOC410860) Antikörper
  • ceroid-lipofuscinosis, neuronal 3 L homeolog (cln3.L) Antikörper
  • uncharacterized LOC467935 (LOC467935) Antikörper
  • AI323623 Antikörper
  • bts Antikörper
  • GB12798 Antikörper
  • JNCL Antikörper
  • MGC80041 Antikörper
  • zgc:92244 Antikörper

Bezeichner auf Proteinebene für CLN3

batten disease protein , battenin , Cln3p , ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease) , ceroid-lipofuscinosis, neuronal 3 , ceroid-lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease) , ceroid-lipofuscinosis, neuronal 3, juvenile , battenin-like

GENE ID SPEZIES
1201 Homo sapiens
12752 Mus musculus
492340 Danio rerio
6343873 Pyrenophora tritici-repentis Pt-1C-BFP
293485 Rattus norvegicus
410860 Apis mellifera
446498 Xenopus laevis
467935 Pan troglodytes
479794 Canis lupus familiaris
504799 Bos taurus
100009244 Oryctolagus cuniculus
100124328 Xenopus (Silurana) tropicalis
100127354 Sus scrofa
100388249 Callithrix jacchus
100457403 Pongo abelii
100583151 Nomascus leucogenys
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