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.