NEU1 anticorps (AA 156-415)

N° du produit ABIN6144538

Cet anticorps Lapin Polyclonal détecte spécifiquement NEU1 dans WB et IHC. Il présente une réactivité envers Humain.

Aperçu rapide pour NEU1 anticorps (AA 156-415) (ABIN6144538)

Antigène: NEU1 (Sialidase 1 (Lysosomal Sialidase) (NEU1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NEU1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-NEU1 anticorps

Épitope: AA 156-415

Séquence: SLCAHKAGCQ VASTMLVWSK DDGVSWSTPR NLSLDIGTEV FAPGPGSGIQ KQREPRKGRL IVCGHGTLER DGVFCLLSDD HGASWRYGSG VSGIPYGQPK QENDFNPDEC QPYELPDGSV VINARNQNNY HCHCRIVLRS YDACDTLRPR DVTFDPELVD PVVAAGAVVT SSGIVFFSNP AHPEFRVNLT LRWSFSNGTS WRKETVQLWP GPSGYSSLAT LEGSMDGEEQ APQLYVLYEK GRNHYTESIS VAKISVYGTL

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 156-415 of human NEU1 (NP_000425.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur NEU1

Antigène: NEU1 (Sialidase 1 (Lysosomal Sialidase) (NEU1))

Autre désignation: NEU1

Sujet: The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity.,NEU1,NANH,NEU,SIAL1,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,NEU1

Poids moléculaire: 45 kDa

ID gène: 4758

UniProt: Q99519

Pathways: SARS-CoV-2 Protein Interactome