SLC19A2 anticorps (AA 21-120) (AbBy Fluor® 555)
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- Antigène Voir toutes SLC19A2 Anticorps
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
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Épitope
- AA 21-120
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Reactivité
- Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SLC19A2 est conjugé à/à la AbBy Fluor® 555
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Specificité
- Possible cross-reactivity with SLC19A3 in human samples
- Réactivité croisée
- Souris
- Homologie
- Human,Rat,Dog,Cow,Pig,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human SLC19A2
- Isotype
- IgG
- Top Product
- Discover our top product SLC19A2 Anticorps primaire
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- Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
- Autre désignation
- SLC19A2 (SLC19A2 Produits)
- Synonymes
- anticorps SLC19A2, anticorps TC1, anticorps THMD1, anticorps THT1, anticorps THTR1, anticorps TRMA, anticorps solute carrier family 19 member 2, anticorps solute carrier family 19 (thiamine transporter), member 2, anticorps Slc19a2, anticorps SLC19A2, anticorps slc19a2
- Sujet
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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]
- ID gène
- 10560
- UniProt
- O60779
- Pathways
- Dicarboxylic Acid Transport
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