SUMF1 Antikörper (N-Term)

Produktnummer ABIN2789756

Produktdetails anti-SUMF1 Antikörper

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

Bindungsspezifität: N-Term

Reaktivität: Human, Maus, Ratte, Rind (Kuh), Hund, Pferd, Meerschweinchen, Kaninchen

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SUMF1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: SREANAPGPV PGERQLAHSK MVPIPAGVFT MGTDDPQIKQ DGEAPARRVT

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

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

Aufreinigung: Affinity Purified

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

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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 repeat 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 SUMF1

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

Andere Bezeichnung: SUMF1 (SUMF1 Produkte)

Synonyme: AAPA3037 antikoerper, FGE antikoerper, AA543204 antikoerper, AI463102 antikoerper, AI851573 antikoerper, sulfatase modifying factor 1 antikoerper, SUMF1 antikoerper, Sumf1 antikoerper

Hintergrund: 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

Molekulargewicht: 41 kDa

Gen-ID: 285362

NCBI Accession: NM_182760, NP_877437

UniProt: Q8NBK3