SUMF1 anticorps (N-Term)

N° du produit ABIN2789756

Cet anticorps Lapin Polyclonal détecte spécifiquement SUMF1 dans WB. Il présente une réactivité envers Humain, Souris, Boeuf (Vache), Chien, Rat, Cobaye, Cheval et Lapin.

Aperçu rapide pour SUMF1 anticorps (N-Term) (ABIN2789756)

Antigène: SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))

Reactivité: Humain, Souris, Boeuf (Vache), Chien, Rat, Cobaye, Cheval, Lapin

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SUMF1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SUMF1 anticorps

Épitope: N-Term

Séquence: SREANAPGPV PGERQLAHSK MVPIPAGVFT MGTDDPQIKQ DGEAPARRVT

Homologie: Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 93%, Rabbit: 100%, Rat: 100%

Attributs du produit: This is a rabbit polyclonal antibody against SUMF1. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N-terminal region of Human SUMF1

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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 repeat 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 SUMF1

Antigène: SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))

Autre désignation: SUMF1

Sujet: This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants.
Alias Symbols: AAPA3037, FGE
Protein Interaction Partner: UBC,
Protein Size: 374

Poids moléculaire: 41 kDa

ID gène: 285362

NCBI Accession: NM_182760, NP_877437

UniProt: Q8NBK3