SLC19A2 Antikörper (C-Term)

Produktnummer ABIN971707

Produktdetails anti-SLC19A2 Antikörper

Target: SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))

Bindungsspezifität: C-Term

Reaktivität: Human, Pferd, Kaninchen, Meerschweinchen, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC19A2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: LGLEITTQFL IYASYFALIA VVFLASGAVS VMKKCRKLED PQSSSQVTTS

Homologie: Guinea Pig: 79%, Horse: 86%, Human: 100%, Rabbit: 79%, Rat: 86%

Produktmerkmale: This is a rabbit polyclonal antibody against SLC19A2. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Anwendungsinformationen

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

Kommentare:

Antigen size: 497 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 SLC19A2

Target: SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))

Andere Bezeichnung: SLC19A2 (SLC19A2 Produkte)

Synonyme: SLC19A2 antikoerper, TC1 antikoerper, THMD1 antikoerper, THT1 antikoerper, THTR1 antikoerper, TRMA antikoerper, solute carrier family 19 member 2 antikoerper, solute carrier family 19 (thiamine transporter), member 2 antikoerper, Slc19a2 antikoerper, SLC19A2 antikoerper, slc19a2 antikoerper

Hintergrund: This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.
Alias Symbols: TC1, THT1, THTR1, TRMA, THMD1
Protein Interaction Partner: UBC, CERS2, ELAVL1,
Protein Size: 497

Molekulargewicht: 55 kDa

Gen-ID: 10560

NCBI Accession: NM_006996, NP_008927

UniProt: O60779

Pathways: Dicarboxylic Acid Transport