LYZ anticorps (C-Term)

N° du produit ABIN2788394

L’anticorps Lapin Polyclonal anti-LYZ a été validé pour WB. Il convient pour détecter LYZ dans des échantillons de Humain et Cobaye.

Aperçu rapide pour LYZ anticorps (C-Term) (ABIN2788394)

Antigène: LYZ (Lysozyme (LYZ))

Reactivité: Humain, Cobaye

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LYZ est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-LYZ anticorps

Épitope: C-Term

Séquence: HLSCSALLQD NIADAVACAK RVVRDPQGIR AWVAWRNRCQ NRDVRQYVQG

Homologie: Cow: 50%, Guinea Pig: 77%, Horse: 0%, Human: 100%

Attributs du produit: This is a rabbit polyclonal antibody against LYZ. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the C terminal region of human LYZ

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 148 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur LYZ

Antigène: LYZ (Lysozyme (LYZ))

Autre désignation: LYZ

Sujet: LYZ is a human lysozyme, whose natural substrate is the bacterial cell wall peptidoglycan (cleaving the beta[1-4]glycosidic linkages between N-acetylmuramic acid and N-acetylglucosamine). Lysozyme is one of the anti-microbial agents found in human milk, and is also present in spleen, lung, kidney, white blood cells, plasma, saliva, and tears. Missense mutations in LYZ have been identified in heritable renal amyloidosis.
Alias Symbols: LZM, lysozyme
Protein Interaction Partner: TP53, FUS, NEDD1, CEP57, AURKA, STAU1, SMAD6, UBC, GRK5, CRK, CLU, COPS6, CUL4B, CDK2, PARP11, USP25, USP1, LCN1, LTF, ELN, A2M, LRRK1, NME2, KHK,
Protein Size: 148

Poids moléculaire: 15 kDa

ID gène: 4069

NCBI Accession: NM_000239, NP_000230

UniProt: P61626