SLC19A2 Antikörper (C-Term)
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- Target Alle SLC19A2 Antikörper anzeigen
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
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Bindungsspezifität
- C-Term
- Reaktivität
- Human, Pferd, Kaninchen, Meerschweinchen, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SLC19A2 Antikörper ist unkonjugiert
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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
- Top Product
- Discover our top product SLC19A2 Primärantikörper
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- Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator.
- Kommentare
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Antigen size: 497 AA
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- 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.
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- 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
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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
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