catalog number :
MBS9324092
products type :
ELISA Kit
products full name :
Human Major facilitator superfamily domain-containing protein 2A, MFSD2 ELISA Kit
products short name :
major facilitator superfamily domain containing 2
products name syn :
Human Major facilitator superfamily domain-containing protein 2A (MFSD2) ELISA kit; FLJ14490; FLJ35904; MFSD2; major facilitator superfamily domain containing 2; major facilitator superfamily domain containing 2
other names :
sodium-dependent lysophosphatidylcholine symporter 1 isoform 1; Sodium-dependent lysophosphatidylcholine symporter 1; sodium-dependent lysophosphatidylcholine symporter 1; sodium-dependent LPC symporter 1; major facilitator superfamily domain-containing protein 2A; major facilitator superfamily domain containing 2A; Major facilitator superfamily domain-containing protein 2A
products gene name :
MFSD2
other gene names :
MFSD2A; MFSD2A; NLS1; MFSD2; MFSD2; NLS1; HMFN0656; PP9177; UNQ300/PRO341; NLS1; Sodium-dependent LPC symporter 1
uniprot entry name :
NLS1_HUMAN
specificity :
No significant cross-reactivity or interference between Human MFSD2A and analogues was observed.
storage stability :
Store all reagents at 2-8 degree C
other info1 :
Samples: Serum, Plasma, Tissue Homogenate, Feces and Urine. Assay Type: Sandwich. Detection Range: 31.2 pg/ml - 1000 pg/ml. Sensitivity: 5.0 pg/ml.
other info2 :
Intended Uses: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! It is intended to be determinated MFSD2A concentrations in Human serum, plasma and other body fluids. Using Purified Human MFSD2A antibody to coat Microelisa Stripplate wells to make solid-phase antibody, then add MFSD2A and MFSD2A antibody which has been labeled with HRP to wells, then the reactants become antibody-antigen-antibody-enzyme complex, after washing completely, add TMB substrate solution, TMB substrate becomes blue color under HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of MFSD2A in the samples is then determined by comparing the O.D. of the samples to the standard curve. Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100]
products description :
Background: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! It is intended to be determinated MFSD2A concentrations in Human serum, plasma and other body fluids. Using Purified Human MFSD2A antibody to coat Microelisa Stripplate wells to make solid-phase antibody, then add MFSD2A and MFSD2A antibody which has been labeled with HRP to wells, then the reactants become antibody-antigen-antibody-enzyme complex, after washing completely, add TMB substrate solution, TMB substrate becomes blue color under HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of MFSD2A in the samples is then determined by comparing the O.D. of the samples to the standard curve.
ncbi acc num :
NP_001129965.1
ncbi gb acc num :
NM_001136493.2
ncbi mol weight :
60,170 Da
uniprot summary :
MFSD2: Plays a role in thermogenesis via beta-adrenergic signaling pathway. May be the main plasma membrane tunicamycin transporter. Belongs to the major facilitator superfamily. 3 isoforms of the human protein are produced by alternative splicing. Protein type: Membrane protein, multi-pass; Membrane protein, integral. Chromosomal Location of Human Ortholog: 1p34.2. Cellular Component: endoplasmic reticulum membrane; integral to plasma membrane; cytoplasm; plasma membrane. Molecular Function: phospholipid transporter activity; symporter activity. Biological Process: phospholipid transport; transcytosis; transmembrane transport; fatty acid transport. Disease: Microcephaly 15, Primary, Autosomal Recessive