Comparison

SLC17A5 Antibody

Item no. PRS-29-924-100ul
Manufacturer ProSci
Amount 100 ul
Category
Type Antibody Polyclonal
Format Liquid
Applications WB, IHC, ELISA
Specific against Human, Mouse, Rat
Host Rabbit
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias SLC17A5, AST, FLJ22227, FLJ23268, ISSD, NSD, SD, SIALIN, SIASD, SLD
Available
Shipping
blue ice or RT
By Research Area
Membrane
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SLC17A5.
Applications
SLC17A5 antibody can be used for detection of SLC17A5 by ELISA at 1:1562500. SLC17A5 antibody can be used for detection of SLC17A5 by western blot at 0.5 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.
Positive Control 1
Tranfected 293T Cell Lysate
Predicted Molecular Weight
55 kDa
Purification
Antibody is purified by peptide affinity chromatography method.
Clonality
Polyclonal
Conjugate
Unconjugated
Buffer
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration
batch dependent
Storage Conditions
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store SLC17A5 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Disclaimer
This product is for research use only.
Modifications
None
Ncbi Official Symbol
SLC17A5
Accession #
NP_036566
Protein Gi #
6912666
Ncbi Gene Id #
26503
User Note
Optimal dilutions for each application to be determined by the researcher.
Ncbi Official Symbol
SLC17A5
Ncbi Official Full Name
solute carrier family 17 (acidic sugar transporter), member 5
Ncbi Organism
Homo sapiens
Swissprot #
Q9NRA2
Background
SLC17A5 is a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in SLC17A5 gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form.This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Background References 1
Myall, N.J., (2007) Mol. Genet. Metab. 92 (4), 371-374.
1st Image Caption
Antibody used in IHC on Human Muscle.
2nd Image Caption
Antibody used in WB on Human 293T at 0.5 ug/ml.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ul
Available: In stock
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