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Anti-Human SLC13A3 Polyclonal Antibody (HB405014)

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Overview
Catalog No.HB405014
Description
Highlights
  • Affinity Purified — Minimal background and high purity for reliable results.
  • Multi-Application — Validated across multiple applications.
Species reactivityHuman
ApplicationsELISA, IHC, WB
Host speciesRabbit
IsotypeIgG
Clonality Polyclonal
Immunogen E. coli - derived recombinant human SLC13A3 (Ile158-Ile230).
Target Na(+)/dicarboxylate cotransporter 3; NaDC-3; hNaDC3; Na(+)-coupled carboxylate transporter 3; NaC3; Sodium-dependent high-affinity dicarboxylate transporter 2; Solute carrier family 13 member 3; SLC13A3; SLC13A3; NADC3; SDCT2
Endotoxin level Please contact with the lab for this information.
Purification Purified by antigen affinity column.
Accession Q8WWT9
Form Liquid
Storage buffer 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Product Usage Information
Application Dilution
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Background

Na(+)/dicarboxylate cotransporter 3 (SLC13A3) is a ~66 kDa protein. High-affinity sodium-dicarboxylate cotransporter that accepts a range of substrates with 4-6 carbon atoms, such as the citric acid cycle intermediates succinate and alpha-ketoglutarate (2-oxoglutarate), as well as other compounds including N-acetyl-L-aspartate. Transports the dicarboxylate into the cell with a probable stoichiometry of 3 Na(+) for 1 divalent dicarboxylate, rendering the process electrogenic. Can transport citrate in a Na(+)-dependent manner, recognizing the divalent form of citrate rather than the trivalent form which is normally found in blood. Imports itaconate in hepatocytes leading to activation of TFEB-dependent lysosomal biogenesis involved in antibacterial innate immune response.

1. Wang, H. et al. (2000) American journal of physiology. Cell physiology 278, C1019-30. PMID: 10794676
2. Huang, W. et al. (2000) The Journal of pharmacology and experimental therapeutics 295, 392-403. PMID: 10992006
3. Burckhardt, BC. et al. (2005) American journal of physiology. Renal physiology 288, F792-9. PMID: 15561973
4. Stellmer, F. et al. (2007) Journal of molecular medicine (Berlin, Germany) 85, 763-70. PMID: 17356845
5. Bai, XY. et al. (2007) FASEB journal : official publication of the Federation of American Societies for Experimental Biology 21, 2409-17. PMID: 17426067
6. Schorbach, L. et al. (2013) Nephron. Physiology 124, 1-5. PMID: 24247155
7. Dewulf, JP. et al. (2019) Annals of neurology 85, 385-395. PMID: 30635937
8. Li, Y. et al. (2025) Nature structural & molecular biology 32, 502-512. PMID: 39622972
9. Chen, C. et al. (2024) Developmental cell 59, 2807-2817.e8. PMID: 39116875
Note For research use only
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Formula
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