anti-TPP1 (TPP1) Antikörper

Bezeichnung:: anti-Tripeptidyl Peptidase I Antikörper (TPP1)

Auf www.antikoerper-online.de finden Sie aktuell 116 Tripeptidyl Peptidase I (TPP1) Antikörper von 22 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen TPP1 Kits (26) und TPP1 Proteine (16) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 166 TPP1 Produkte verfügbar.

Synonyme:: Cln2, fa01b09, im:7149243, LPIC, TPP-1, TPP-I, wu:fa01b09

Alle Antikörper anzeigen	Gen	GeneID	UniProt
	TPP1	1200	O14773
	TPP1	83534	Q9EQV6
	TPP1	12751	O89023
Alle Spezies anzeigen Weitere Synonyme anzeigen

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anti-Rat (Rattus) TPP1 Antikörper:

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Am meisten referenzierte anti-TPP1 Antikörper

Human Polyclonal TPP1 Primary Antibody für IF (p) - ABIN1417442 : Brenneman, Pearce, Kovacs, DeFrees: Pharmacological Effects on Ceroid Lipofuscin and Neuronal Structure in Cln3∆ex7/8Mouse Brain Cultures. in Journal of molecular neuroscience : MN 2017 (PubMed)
Human Monoclonal TPP1 Primary Antibody für IHC (p), ELISA - ABIN560411 : Qing, Zhou, Zhao, Xie, Yang, Xing, Zeng, Jiang: Altered expression of TPP1 in fibroblast-like synovial cells might be involved in the pathogenesis of rheumatoid arthritis. in Rheumatology international 2012 (PubMed)
Human Polyclonal TPP1 Primary Antibody für ICC, IF - ABIN451783 : Kousi, Siintola, Dvorakova, Vlaskova, Turnbull, Topcu, Yuksel, Gokben, Minassian, Elleder, Mole, Lehesjoki: Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis. in Brain : a journal of neurology 2009 (PubMed)

Weitere Antikörper gegen TPP1 Interaktionspartner

Human Tripeptidyl Peptidase I (TPP1) Interaktionspartner

The reports the crystal structure of the N-terminal domain of TIN2 (zeige TINF2 Antikörper) in complex with TIN2 (zeige TINF2 Antikörper)-binding motifs from TPP1 and TRF2 (zeige TERF2 Antikörper), revealing how TIN2 (zeige TINF2 Antikörper) interacts cooperatively with TPP1 and TRF2 (zeige TERF2 Antikörper).
TPP1 cleaves and destabilizes fibrillar amyloid-beta at multiple sites in a time- and pH-dependent manner.
To confirm clinical suspicion of CLN2 disease, the recommended gold standard for laboratory diagnosis is demonstration of deficient TPP1 enzyme activity (in leukocytes, fibroblasts, or dried blood spots) and the identification of causative mutations in each allele of the TPP1/CLN2 gene.
These studies indicate that optimal treatment outcomes for CLN2 disease may require delivery of TPP1 systemically as well as directly to the central nervous system.
TPP1 is overexpressed in hepatocellular carcinoma tissues and significantly correlated with poor prognosis of hepatocellular carcinoma patients.RFX5 acts as a direct positive transcriptional regulator of TPP1 in hepatocellular carcinoma.
TPP1(CLN2) mutation is associated with neuronal ceroid lipofuscinosis (zeige CLN6 Antikörper).
To our knowledge, our results bring the first evidence of a mechanism that links TPP-1 deficiency and oxidative stress-induced (zeige SQSTM1 Antikörper) changes in mitochondrial morphology.
hypothesize that loss of function variants abolishing TPP1 enzyme activity lead to CLN2 disease, whereas variants that diminish TPP1 enzyme activity lead to SCAR7
This study demonistrated that the CLN2 gene 4 mutation in late infantile neuronal ceroid lipofuscinosis (zeige CLN6 Antikörper).
TPP1 mutants utilize the advantages of a zebrafish model for understanding the pathogenesis of late infantile (or classic late infantile neuronal ceroid lipofuscinosis (zeige CLN6 Antikörper)) disease.

Mouse (Murine) Tripeptidyl Peptidase I (TPP1) Interaktionspartner

telomeres are protected from hyper-resection through the repression of the ATM (zeige ATM Antikörper) and ATR (zeige ATR Antikörper) kinases by TRF2 (zeige TERF2 Antikörper) and TPP1-bound POT1a (zeige POT1 Antikörper)/b, respectively.
Rssults suggested that CLN2, CLN3 (zeige CLN3 Antikörper) and CLN5 (zeige CLN5 Antikörper) genes may play an important role in early embryonal neurogenesis.
demonstrated that cells expressing TIN2DeltaTPP1 instead of wild-type TIN2 (zeige TINF2 Antikörper) phenocopy the POT1a (zeige POT1 Antikörper),b knockout setting without showing additional phenotypes
Gemfibrozil and fenofibrate, Food and Drug Administration-approved lipid-lowering drugs, up-regulate tripeptidyl-peptidase 1 in brain cells via peroxisome proliferator-activated receptor alpha (zeige PPARA Antikörper) and may have implications in late infantile Batten disease therapy
TPPI activity becomes crucial for the neuronal functions later in development.
Telomere protection by TPP1/POT1 (zeige POT1 Antikörper) requires tethering to TIN2 (zeige TINF2 Antikörper).
TPP1 protects telomere integrity and regulates telomerase recruitment to telomeres, thereby preventing early occurrence of degenerative skin pathologies.
TPP1 deletion resulted in the release of POT1a (zeige POT1 Antikörper) and POT1b from chromatin and loss of these proteins from telomeres, indicating that TPP1 is required for the telomere association of POT1a (zeige POT1 Antikörper) and POT1b but not for their stability.
Lysosomal degradation of cholecystokinin (zeige CCK Antikörper)-(29-33)-amide in mouse brain is dependent on this enzyme: implications for the degradation and storage of peptides in classical late-infantile neuronal ceroid lipofuscinosis (zeige CLN6 Antikörper) (tripeptidyl peptidase-I)
TPP-I is the predominant proteolytic enzyme responsible for the intracellular degradation of neuromedin B

TPP1 Antigen-Profil

Beschreibung des Gens

This gene encodes a member of the sedolisin family of serine proteases. The protease functions in the lysosome to cleave N-terminal tripeptides from substrates, and has weaker endopeptidase activity. It is synthesized as a catalytically-inactive enzyme which is activated and auto-proteolyzed upon acidification. Mutations in this gene result in late-infantile neuronal ceroid lipofuscinosis, which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome.

Alternative names and synonyms associated with TPP1

tripeptidyl peptidase I (tpp1) Antikörper
tripeptidyl-peptidase 1 (NAEGRDRAFT_78259) Antikörper
tripeptidyl-peptidase 1 (MCYG_00184) Antikörper
tripeptidyl-peptidase 1 (MGYG_05881) Antikörper
tripeptidyl-peptidase 1 (MGYG_00757) Antikörper
tripeptidyl peptidase 1 (tpp1) Antikörper
tripeptidyl peptidase 1 (TPP1) Antikörper
tripeptidyl peptidase 1 (Tpp1) Antikörper
tripeptidyl peptidase I (Tpp1) Antikörper

Cln2 Antikörper
fa01b09 Antikörper
im:7149243 Antikörper
LPIC Antikörper
TPP-1 Antikörper
TPP-I Antikörper
wu:fa01b09 Antikörper

Bezeichner auf Proteinebene für TPP1

ceroid-lipofuscinosis, neuronal 2 , tripeptidyl-peptidase 1 , cell growth-inhibiting gene 1 protein , growth-inhibiting protein 1 , lysosomal pepstatin insensitive protease , tripeptidyl aminopeptidase , LPIC , TPP-1 , TPP-I , lysosomal pepstatin-insensitive protease , tripeptidyl peptidase 1 , tripeptidyl-peptidase I , tripeptidyl peptidase-I

GENE ID	SPEZIES
798347	Danio rerio
8862382	Naegleria gruberi strain NEG-M
9230210	Arthroderma otae CBS 113480
10026584	Arthroderma gypseum CBS 118893
10031989	Arthroderma gypseum CBS 118893
100195058	Salmo salar
1200	Homo sapiens
485337	Canis lupus familiaris
515575	Bos taurus
83534	Rattus norvegicus
12751	Mus musculus
425576	Gallus gallus
100356773	Oryctolagus cuniculus
100733945	Cavia porcellus
450999	Pan troglodytes
100440001	Pongo abelii

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Show all anti-Tripeptidyl Peptidase I (TPP1) Antikörper with Pubmed References

Human Tripeptidyl Peptidase I (TPP1) Interaktionspartner

Mouse (Murine) Tripeptidyl Peptidase I (TPP1) Interaktionspartner

Beschreibung des Gens

Alternative names and synonyms associated with TPP1

Bezeichner auf Proteinebene für TPP1