Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) (N-Term) antibody

Details for Product No. ABIN310524
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Antigen
Synonyms AST, ISSD, NSD, SD, SIALIN, SIASD, SLD, sialin, 4631416G20Rik, 4732491M05, SP55
Epitope
N-Term
(2), (1), (1), (1)
Reactivity
Rabbit, Mouse (Murine), Rat (Rattus), Xenopus laevis, Dog (Canine), Cow (Bovine), Human, Chicken
(10), (3), (3)
Host
Rabbit
(7), (3)
Clonality
Polyclonal
Application
Immunohistochemistry (IHC), Western Blotting (WB)
(9), (4), (3), (2), (2), (1), (1)
Pubmed 1 reference available
Quantity 50 µg
Options
Shipping to United States (Change)
Availability Will be delivered in 2 to 3 Business Days
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Catalog No. ABIN310524
289.00 $
Plus shipping costs $45.00

Order hotline:

  • +1 404 474 4654
  • +1 888 205 9894 (TF)
Immunogen Synthetic peptide directed towards the N terminal of human SLC17A5
Sequence LFTPIAADLG VGPLIVLRAL EGLGEGVTFP AMHAMWSSWA PPLERSKLLS
Predicted Reactivity African clawed frog : 100 %, Bovine : 100 %, Chicken : 100 %, Dog : 100 %, Guinea pig : 100 %, Horse : 100 %, Human : 100 %, Rabbit : 100 %, Rat : 100 %, Zebrafish : 70 %
Characteristics This is a rabbit polyclonal antibody against SLC17A5. It was validated on Western Blot and immunohistochemistry.
Purification Affinity Purified
Alternative Name SLC17A5
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.
Molecular Weight 55 kDa
Gene ID 26503
NCBI Accession NP_036566, NM_012434
UniProt Q9NRA2
Research Area Signaling, Metabolism
Application Notes Optimal working dilutions should be determined experimentally by the investigator.
Comment

Antigen size: 495 AA

Restrictions For Research Use only
Format Lyophilized
Reconstitution Add 50 µL of distilled water.
Concentration 1 mg/mL
Buffer PBS buffer with 2 % sucrose
Handling Advice Avoid repeated freeze-thaw cycles.
Storage -20 °C
Storage Comment For longer periods of storage, store at -20 °C
Supplier Images
anti-Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) (N-Term) antibody anti-Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) (N-Term) antibody
anti-Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) (N-Term) antibody (2) anti-Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) (N-Term) antibody (Image 2)
Background publications Myall, Wreden, Wlizla et al.: "G328E and G409E sialin missense mutations similarly impair transport activity, but differentially affect trafficking." in: Molecular genetics and metabolism, Vol. 92, Issue 4, pp. 371-4, 2007 (PubMed).

Validation Images
Did you look for something else?
back to top