SUMF1 anticorps (N-Term)

N° du produit ABIN2789756

Détail du produit anti-SUMF1 anticorps

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

Épitope: N-Term

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SUMF1 est non-conjugé

Application: Western Blotting (WB)

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 (SUMF1 Produits)

Synonymes: anticorps AAPA3037, anticorps FGE, anticorps AA543204, anticorps AI463102, anticorps AI851573, anticorps sulfatase modifying factor 1, anticorps SUMF1, anticorps 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