Arylsulfatase E anticorps (Middle Region)

N° du produit ABIN2776926

L’anticorps anti-Arylsulfatase E Polyclonal Lapin est utilisé pour la détection de Arylsulfatase E dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour Arylsulfatase E anticorps (Middle Region) (ABIN2776926)

Antigène: Arylsulfatase E (ARSE)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Arylsulfatase E est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Arylsulfatase E anticorps

Épitope: Middle Region

Fonction: ARSE Antibody - middle region

Séquence: KVVHHDPPLL FDLSRDPSET HILTPASEPV FYQVMERVQQ AVWEHQRTLS

Homologie: Human: 100%

Attributs du produit: This is a rabbit polyclonal antibody against ARSE. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of human ARSE

Information d'application

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

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP41665-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

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

Détails sur Arylsulfatase E

Antigène: Arylsulfatase E (ARSE)

Autre désignation: ARSE

Sujet:

Background Information: Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-170 AC005295.1 87561-87730 c 171-744 AK223183.1 1-574 745-2036 AK223199.1 542-1833 2037-2220 AW779826.1 1-184 c

Gene Name: Arylsulfatase E (chondrodysplasia punctata 1)

Alternative Symbols: ASE, ARSE, CDPX, CDPX1, CDPXR

Protein Name: Arylsulfatase E

Poids moléculaire: 62kDa

ID gène: 415

NCBI Accession: NP_000038

UniProt: P51690