IDUA anticorps (C-Term)
-
- Antigène Voir toutes IDUA Anticorps
- IDUA (Iduronidase, alpha-L- (IDUA))
-
Épitope
- C-Term
-
Reactivité
- Humain, Souris, Rat, Cobaye, Cheval, Boeuf (Vache), Chien
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp IDUA est non-conjugé
-
Application
- Western Blotting (WB)
- Séquence
- DPVAAAPRPL PAGGRLTLRP ALRLPSLLLV HVCARPEKPP GQVTRLRALP
- Homologie
- Cow: 93%, Dog: 93%, Guinea Pig: 86%, Horse: 100%, Human: 100%, Mouse: 86%, Rat: 80%
- Attributs du produit
- This is a rabbit polyclonal antibody against IDUA. It was validated on Western Blot.
- Purification
- Affinity Purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the C-terminal region of Human IDUA
- Top Product
- Discover our top product IDUA Anticorps primaire
-
-
- Restrictions
- For Research Use only
-
- 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.
-
- Antigène
- IDUA (Iduronidase, alpha-L- (IDUA))
- Autre désignation
- IDUA (IDUA Produits)
- Synonymes
- anticorps IDA, anticorps MPS1, anticorps 6030426D08, anticorps alpha-L-iduronidase, anticorps MGC80842, anticorps si:ch211-12e13.9, anticorps IDUA, anticorps iduronidase, alpha-L-, anticorps iduronidase, alpha-L- L homeolog, anticorps alpha-L-iduronidase, anticorps IDUA, anticorps Idua, anticorps idua.L, anticorps idua, anticorps LOC5564727
- Sujet
-
This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I).
Protein Interaction Partner: MPP3,
Protein Size: 675 - Poids moléculaire
- 74 kDa
- ID gène
- 3425
- UniProt
- P35475
- Pathways
- Glycosaminoglycan Metabolic Process
-