SLC19A2 monoclonal antibody (M10), clone 5B10
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More Files
- More Functions
Western Blot (Tissue lysate)
SLC19A2 monoclonal antibody (M10), clone 5B10. Western Blot analysis of SLC19A2 expression in human pancreas.
Sandwich ELISA (Recombinant protein)
Detection limit for recombinant GST tagged SLC19A2 is approximately 0.1ng/ml as a capture antibody.
Western Blot detection against Immunogen (34.21 KDa) .
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Specification
Product Description
Mouse monoclonal antibody raised against a partial recombinant SLC19A2.
Immunogen
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.
Sequence
PMPQKSLFFHHIPSTCQRVNGIKVQNGGIVTDTPASNHLPGWEDIESKIPLNMEEPPVEEPEPKPDRLLVLKVLWND
Host
Mouse
Reactivity
Human
Isotype
IgG2a Kappa
Quality Control Testing
Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (34.21 KDa) .
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Tissue lysate)
SLC19A2 monoclonal antibody (M10), clone 5B10. Western Blot analysis of SLC19A2 expression in human pancreas.Western Blot (Recombinant protein)
Sandwich ELISA (Recombinant protein)
Detection limit for recombinant GST tagged SLC19A2 is approximately 0.1ng/ml as a capture antibody.ELISA
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Gene Info — SLC19A2
Entrez GeneID
10560GeneBank Accession#
NM_006996.1Protein Accession#
NP_008927.1Gene Name
SLC19A2
Gene Alias
TC1, THT1, THTR1, TRMA
Gene Description
solute carrier family 19 (thiamine transporter), member 2
Gene Ontology
HyperlinkGene Summary
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
Other Designations
OTTHUMP00000033497|high affinity thiamine transporter|reduced folate carrier protein (RFC) like|solute carrier family 19, member 2|thiamine transporter 1
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Interactome
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Disease
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