SKU: WP2858 Categories: ,

MFSD8 Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP2858-100
Enter the quantity you would like, or drag the panel to find the quantity and price that best for you
Bulk QuoteAuthorize OEM & ODM

Product details

Background:

This gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. The substrate transported by this protein is unknown. The protein likely localizes to lysosomal membranes. Mutations in this gene are correlated with a variant form of late infantile-onset neuronal ceroid lipofuscinoses (vLINCL). [provided by RefSeq, Oct 2008],

Specifications

Size50μL/100μL
TargetMFSD8
ReactivityHuman, Mouse
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)56kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; ELISA 1:5000-20000
FormulationLiquid in PBS containing 50% glycerol,0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human protein . at AA range: 351-400
SpecificityMFSD8 Polyclonal Antibody detects endogenous levels of protein.
Gene NameMFSD8 CLN7
Protein NameMajor facilitator superfamily domain-containing protein 8 (Ceroid-lipofuscinosis neuronal protein 7)
Other Name
SpeciesHuman
Gene ID256471
UniprotQ8NHS3,
Species.1Mouse
Gene ID.1
Uniprot.1Q8BH31
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationLysosome membrane; Multi-pass membrane protein . Sorting to lysosomes involves tyrosine- and/or dileucine-based motifs.
Tissue ExpressionExpressed at very low levels in all tissues tested.
Signaling_pathwayCellular Processes >> Transport and catabolism >> Lysosome
Research Areas>>Lysosome
FunctionDisease:Defects in MFSD8 are the cause of neuronal ceroid lipofuscinosis type 7 (CLN7) [MIM:610951]. CNL are a clinically and genetically heterogeneous group of neurodegenerative disorders characterized by the intracellular accumulation of autofluorescent lipopigment storage material in different patterns ultrastructurally. The patterns most often observed CLN7 are mixed combinations of granular, curvilinear, fingerprint, and rectilinear profiles. The clinical course includes progressive dementia, seizures, and progressive visual failure.,Function:May be a carrier that transport small solutes by using chemiosmotic ion gradients .,similarity:Belongs to the major facilitator superfamily.,tissue specificity:Expressed at very low levels in all tissues tested.,
Please login to post questions
Back to Top
Product has been added to your cart