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Antibody used in IHC on Human Muscle.
Antibody used in WB on Human 293T at 0.5 ug/ml.
Antibody used in IHC on Human Muscle.

SLC17A5 Antibody

CATALOG NUMBER: 29-924

Clonality:
Polyclonal
Tested Applications:
ELISA, IHC, WB
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SLC17A5.
Conjugate:
Unconjugated
Tested Applications:
ELISA, IHC, WB
Application Note:
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 μg/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
Physical State:
Liquid
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.
Ncbi Official Symbol:
SLC17A5
Additional Names:
SLC17A5, AST, FLJ22227, FLJ23268, ISSD, NSD, SD, SIALIN, SIASD, SLD
Protein Accession Number:
NP_036566
Protein Gi Number:
6912666
Ncbi Gene Id Number:
26503
User Note:
Optimal dilutions for each application to be determined by the researcher.
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 Reference 1:
Myall, N.J., (2007) Mol. Genet. Metab. 92 (4), 371-374.

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

29-924

List Size:
100 ul

List Price:

$519.00

Datasheet
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