SLC19A2 Antikörper (AA 21-120) (AbBy Fluor® 488)
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- Target Alle SLC19A2 Antikörper anzeigen
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
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Bindungsspezifität
- AA 21-120
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Reaktivität
- Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SLC19A2 Antikörper ist konjugiert mit AbBy Fluor® 488
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Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Spezifität
- Possible cross-reactivity with SLC19A3 in human samples
- Kreuzreaktivität
- Maus
- Homologie
- Human,Rat,Dog,Cow,Pig,Horse,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human SLC19A2
- Isotyp
- IgG
- Top Product
- Discover our top product SLC19A2 Primärantikörper
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- Applikationshinweise
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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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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Synonyms: Thiamine transporter 1, S19A2_HUMAN, SLC19A2, Solute carrier family 19 member 2, TC1, Thiamine carrier 1, THT1, ThTr 1, ThTr-1, ThTr1, TRMA.
Background: 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. [provided by RefSeq, Jul 2008]
- Gen-ID
- 10560
- UniProt
- O60779
- Pathways
- Dicarboxylic Acid Transport
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