Arylsulfatase E Antikörper (Middle Region)

Produktnummer ABIN2776926

Produktdetails anti-Arylsulfatase E Antikörper

Target: Arylsulfatase E (ARSE)

Bindungsspezifität: Middle Region

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Arylsulfatase E Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: KVVHHDPPLL FDLSRDPSET HILTPASEPV FYQVMERVQQ AVWEHQRTLS

Homologie: Human: 100%

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

Aufreinigung: Affinity Purified

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

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 589 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: 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.

Details zu Arylsulfatase E

Target: Arylsulfatase E (ARSE)

Andere Bezeichnung: ARSE (ARSE Produkte)

Hintergrund: 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
Alias Symbols: CDPX, CDPX1, CDPXR, MGC163310, ASE
Protein Interaction Partner: COQ6, TMEM259, TNK2, NDN,
Protein Size: 589

Molekulargewicht: 62 kDa

Gen-ID: 415

NCBI Accession: NM_000047, NP_000038

UniProt: P51690