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Unfortunately, the antibody LS-C226390 is no longer available.

Below is a list of antibodies to the same protein target. You may also try your search again using the search box at the top of the page. Please contact us if you have any questions.



SLC19A2 / TC1 Antibodies

solute carrier family 19 (thiamine transporter), member 2

Gene Name: solute carrier family 19 (thiamine transporter), member 2
Family/Subfamily: Transporter , Reduced folate carrier
Synonyms: SLC19A2 Antibody, HTHTR1 Antibody, Thiamine carrier 1 Antibody, THTR1 Antibody, ThTr-1 Antibody, Thiamine transporter 1 Antibody, THMD1 Antibody, TRMA Antibody, TC1 Antibody, THT1 Antibody
Target Sequences: AF160812 AAF15129.1 O60779
 SLC19A2 / TC1 Feature Table

SLC19A2 / TC1 Antibodies (3)

Target Reactivity Applications Host Isotype Clonality Clone Format Epitope Publications Type
SLC19A2 / TC1 Rabbit IgG Polyclonal Unconjugated Human IHC-P, WB No Primary
Anti-SLC19A2 / TC1 Antibody LS-C179211
WB Image
Rabbit Polyclonal (IgG) to Human SLC19A2 / TC1
Human
IHC - Paraffin, Western blot
Unconjugated
SLC19A2 / TC1 Rabbit Polyclonal Unconjugated Human, Chimpanzee, Horse, Rabbit WB C-Terminus No Primary
Anti-SLC19A2 / TC1 Antibody (C-Terminus) LS-C146133
WB Image
Rabbit Polyclonal to Human SLC19A2 / TC1
Human, Chimpanzee, Horse, Rabbit
Western blot
Unconjugated
SLC19A2 / TC1 Mouse IgG2a Monoclonal Unconjugated, Azide-free Human WB, ELISA aa209-286 No
Anti-SLC19A2 / TC1 Antibody (aa209-286, Azide-free) LS-C330666
Mouse Monoclonal (IgG2a) to Human SLC19A2 / TC1
Human
Western blot, ELISA
Unconjugated, Azide-free

SLC19A2 / TC1 Feature Table


Feature Type Location Details
alternative products 1 - 497 Event=Alternative splicing; Named isoforms=2; Name=1; IsoId=O60779-1; Sequence=Displayed; Name=2; IsoId=O60779-2; Sequence=VSP_036467;
Disease 1 - 497 Defects in SLC19A2 are the cause of thiamine-responsive megaloblastic anemia syndrome (TRMA) [MIM:249270]; also known as Rogers syndrome. TRMA is an autosomal recessive disease with features that include megaloblastic anemia, mild thrombocytopenia and leucopenia, sensorineural deafness and diabetes mellitus.
Function 1 - 497 High-affinity transporter for the intake of thiamine.
sequence caution 1 - 497 Sequence=BAG64936.1; Type=Erroneous initiation;
Similarity 1 - 497 Belongs to the reduced folate carrier (RFC) transporter (TC 2.A.48) family.
Subcellular Location 1 - 497 Membrane; Multi-pass membrane protein.
Tissue Specificity 1 - 497 Ubiquitous; most abundant in skeletal and cardiac muscle. Medium expression in placenta, heart, liver and kidney, low in lung.
web resource 1 - 497 Name=GeneReviews; URL="http://www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/SLC19A2";
arrayexpress 1 - 497 O60779
bgee 1 - 497 O60779
cleanex 1 - 497 HS_SLC19A2
ctd 1 - 497 10560
doi 1 - 497 10
eggnog 1 - 497 prNOG19004
embl 1 - 497 AF135488
embl 1 - 497 AF153330
embl 1 - 497 AF158233
embl 1 - 497 AF160186
embl 1 - 497 AF160756
embl 1 - 497 AF160812
embl 1 - 497 AF272359
embl 1 - 497 AJ237724
embl 1 - 497 AJ238413
embl 1 - 497 AK304021
embl 1 - 497 AK313779
embl 1 - 497 AK316465
embl 1 - 497 AL021068
embl 1 - 497 BC018514
embl 1 - 497 CH471067
ensembl 1 - 497 ENST00000236137
genecards 1 - 497 GC01M169433
geneid 1 - 497 10560
genevestigator 1 - 497 O60779
germonline 1 - 497 ENSG00000117479
go 1 - 497 GO:0005542
go 1 - 497 GO:0008517
go 1 - 497 GO:0008518
go 1 - 497 GO:0015234
go 1 - 497 GO:0016021
go 1 - 497 GO:0042723
hgnc 1 - 497 HGNC:10938
hovergen 1 - 497 HBG054198
hpa 1 - 497 HPA006119
hpa 1 - 497 HPA016599
inparanoid 1 - 497 O60779
interpro 1 - 497 IPR002666
interpro 1 - 497 IPR016196
ipi 1 - 497 IPI00031631
ipi 1 - 497 IPI00103058
kegg 1 - 497 hsa:10560
medline 1 - 497 20011385
medline 1 - 497 20334494
medline 1 - 497 99318105
medline 1 - 497 99318106
medline 1 - 497 99318107
mim 1 - 497 249270
mim 1 - 497 603941
nextbio 1 - 497 40077
oma 1 - 497 WEDVESK
orphanet 1 - 497 49827
panther 1 - 497 PTHR10686
pfam 1 - 497 PF01770
pharmgkb 1 - 497 PA35825
phylomedb 1 - 497 O60779
pirsf 1 - 497 PIRSF028739
pride 1 - 497 O60779
proteinmodelportal 1 - 497 O60779
pubmed 1 - 497 10391221
pubmed 1 - 497 10391222
pubmed 1 - 497 10391223
pubmed 1 - 497 10542220
pubmed 1 - 497 10874303
pubmed 1 - 497 14702039
pubmed 1 - 497 15489334
pubmed 1 - 497 16710414
pubmed 1 - 497 19413330
reactome 1 - 497 REACT_11193
refseq 1 - 497 NP_008927.1
string 1 - 497 O60779
supfam 1 - 497 SSF103473
tcdb 1 - 497 2.A.48.2.1
tigrfams 1 - 497 TIGR00806
ucsc 1 - 497 uc001gge.2
unigene 1 - 497 Hs.30246
alt_init; mrna 1 - 497 BAG64936.1
alt_seq; genomic_dna 1 - 497 AAD51280.1
alt_seq; genomic_dna 1 - 497 AAD51283.1
carbohyd 63 - 63 N-linked (GlcNAc...) (Potential)
carbohyd 314 - 314 N-linked (GlcNAc...) (Potential)
chain 1 - 497 Thiamine transporter 1 /FTId=PRO_0000178663.
Modification 492 - 492 Phosphoserine
topo_dom 1 - 28 Cytoplasmic (Potential)
topo_dom 47 - 72 Extracellular (Potential)
topo_dom 92 - 99 Cytoplasmic (Potential)
topo_dom 119 - 128 Extracellular (Potential)
topo_dom 150 - 165 Cytoplasmic (Potential)
topo_dom 186 - 191 Extracellular (Potential)
topo_dom 209 - 285 Cytoplasmic (Potential)
topo_dom 311 - 337 Extracellular (Potential)
topo_dom 355 - 363 Cytoplasmic (Potential)
topo_dom 381 - 386 Extracellular (Potential)
topo_dom 410 - 419 Cytoplasmic (Potential)
topo_dom 444 - 455 Extracellular (Potential)
topo_dom 480 - 497 Cytoplasmic (Potential)
transmem 29 - 46 Helical; (Potential)
transmem 73 - 91 Helical; (Potential)
transmem 100 - 118 Helical; (Potential)
transmem 129 - 149 Helical; (Potential)
transmem 166 - 185 Helical; (Potential)
transmem 192 - 208 Helical; (Potential)
transmem 286 - 310 Helical; (Potential)
transmem 338 - 354 Helical; (Potential)
transmem 364 - 380 Helical; (Potential)
transmem 387 - 409 Helical; (Potential)
transmem 420 - 443 Helical; (Potential)
transmem 456 - 479 Helical; (Potential)
var_seq 69 - 269 Missing (in isoform 2) /FTId=VSP_036467.
variant 93 - 93 D -> H (in TRMA) /FTId=VAR_010249.
variant 143 - 143 S -> F (in TRMA) /FTId=VAR_010250.
variant 172 - 172 G -> D (in TRMA; dbSNP:rs28937595) /FTId=VAR_010248.
keyword 1 - 497 Alternative splicing
keyword 1 - 497 Complete proteome
keyword 1 - 497 Deafness
keyword 1 - 497 Diabetes mellitus
keyword 1 - 497 Disease mutation
keyword 1 - 497 Glycoprotein
keyword 1 - 497 Membrane
keyword 1 - 497 Phosphoprotein
keyword 1 - 497 Transmembrane
keyword 1 - 497 Transmembrane helix
keyword 1 - 497 Transport
Molecular Weight 1 - 497 55400
1 hit 1 - 497 PF01770

If you do not find the reagent or information you require, please contact customer.support@lsbio.com to inquire about additional products in development.

PLEASE NOTE

For RESEARCH USE ONLY. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).


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