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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   SLC19A2 Antibody (monoclonal) (M10)   

SLC19A2 Antibody (monoclonal) (M10)

Mouse monoclonal antibody raised against a partial recombinant SLC19A2.

  • WB - SLC19A2 Antibody (monoclonal) (M10) AT3904a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (34.21 KDa) .
  • WB - SLC19A2 Antibody (monoclonal) (M10) AT3904a
    SLC19A2 monoclonal antibody (M10), clone 5B10 Western Blot analysis of SLC19A2 expression in A-431 ( (Cat # AT3904a )
  • E - SLC19A2 Antibody (monoclonal) (M10) AT3904a
    Detection limit for recombinant GST tagged SLC19A2 is approximately 0.1ng/ml as a capture antibody.
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession O60779
Other Accession NM_006996.1
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG2a Kappa
Clone Names 5B10
Calculated MW 55400 Da
Additional Information
Gene ID 10560
Other Names Thiamine transporter 1, ThTr-1, ThTr1, Solute carrier family 19 member 2, Thiamine carrier 1, TC1, SLC19A2, THT1, TRMA
Target/Specificity SLC19A2 (NP_008927.1, 209 a.a. ~ 285 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsSLC19A2 Antibody (monoclonal) (M10) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas
Citations (0)

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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.


Variation at the NFATC2 Locus Increases the Risk of Thiazolinedinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study. Bailey SD, et al. Diabetes Care, 2010 Jul 13. PMID 20628086.Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. Talmud PJ, et al. Am J Hum Genet, 2009 Nov. PMID 19913121.Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations. Bergmann AK, et al. Pediatr Blood Cancer, 2010 Feb. PMID 19731322.Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study. Ehret GB, et al. Eur J Hum Genet, 2009 Dec. PMID 19536175.Pancreatic beta cells and islets take up thiamin by a regulated carrier-mediated process: studies using mice and human pancreatic preparations. Mee L, et al. Am J Physiol Gastrointest Liver Physiol, 2009 Jul. PMID 19423748.

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$ 315.00
Cat# AT3904a
(40 western blots)
Availability: 7-10 days
Bulk Size
Seasonal Special on Bulk Order
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