catalog number :
MBS9126387
products full name :
SLC5A6 Polyclonal Antibody
products short name :
[SLC5A6]
products name syn :
[SMVT]
other names :
[Sodium-dependent multivitamin transporter; Sodium-dependent multivitamin transporter; sodium-dependent multivitamin transporter; solute carrier family 5 member 6; Na+-dependent multivitamin transporter; Na(+)-dependent multivitamin transporter; solute carrier family 5 (sodium-dependent vitamin transporter), member 6; solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6; Solute carrier family 5 member 6]
products gene name :
[SLC5A6]
other gene names :
[SLC5A6; SLC5A6; SMVT; SMVT; Na(+)-dependent multivitamin transporter]
uniprot entry name :
SC5A6_HUMAN
purity :
Affinity Purification
storage stability :
Store at -20 degree C. Avoid freeze/thaw cycles.
tested application :
Western Blot (WB)
app notes :
WB: 1:500 - 1:2000
image1 heading :
Western Blot (WB)
other info1 :
Source: Rabbit. Species: Human
other info2 :
Immunogen: Recombinant protein of human SLC5A6. Calculated Molecular Weight: 68kDa. Observed MW: 71kDa. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
products categories :
Polyclonal
ncbi pathways :
Biotin Transport And Metabolism Pathway (106257); Defective AMN Causes Hereditary Megaloblastic Anemia 1 Pathway (906000); Defective BTD Causes Biotidinase Deficiency Pathway (906015); Defective CD320 Causes Methylmalonic Aciduria Pathway (906012); Defective CUBN Causes Hereditary Megaloblastic Anemia 1 Pathway (906001); Defective GIF Causes Intrinsic Factor Deficiency Pathway (906004); Defective HLCS Causes Multiple Carboxylase Deficiency Pathway (906014); Defective LMBRD1 Causes Methylmalonic Aciduria And Homocystinuria Type CblF Pathway (906003); Defective MMAA Causes Methylmalonic Aciduria Type CblA Pathway (906010); Defective MMAB Causes Methylmalonic Aciduria Type CblB Pathway (906009)
uniprot summary :
SLC5A6: Transports pantothenate, biotin and lipoate in the presence of sodium. Belongs to the sodium:solute symporter (SSF) (TC 2.A.21) family. Protein type: Transporter, SLC family; Transporter; Membrane protein, integral; Membrane protein, multi-pass. Chromosomal Location of Human Ortholog: 2p23. Cellular Component: membrane; integral to plasma membrane; brush border membrane; plasma membrane; vesicle membrane. Molecular Function: sodium-dependent multivitamin transmembrane transporter activity. Biological Process: pantothenate transport; vitamin metabolic process; transport; pantothenate metabolic process; sodium ion transport; biotin transport; transmembrane transport; biotin metabolic process; water-soluble vitamin metabolic process