SLC13A1 Antibodies

AND SLC13A1 ELISA kits, SLC13A1 Proteins

Many biological assays use antibodies to detect SLC13A1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC13A1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC13A1 antibodies...

We validate the specificity of these antibodies to SLC13A1 by testing them on tissues known to express SLC13A1 positively and negatively. Browse below to find the SLC13A1 antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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SLC13A1 Infographic by Boster Bio

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SLC13A1 Overview

Facts about Solute carrier family 13 member 1.

SLC13A1 3D structure. Source: alphafold

Solute carrier family 13 member 1 (SLC13A1)

Sodium/sulfate cotransporter that mediates sulfate reabsorption in the kidney. .

Gene Information

Human
Gene Name:	SLC13A1
Uniprot:	Q9BZW2
Entrez:	6561

Family

Belongs to:

SLC13A/DASS transporter (TC 2.A.47) family

Alternative Names

solute carrier family 13 member 1; NAS1; NASI1; NaSi-1; SLC13A1; solute carrier family 13 (sodium/sulfate symporters), member 1

Molecular Weight

Mass (kDA):
66.134 kDA

Genomic Context


Human

Location:	7q31.32
Sequence:	7; NC_000007.14 (123113490..123201836, complement)

Tissue Specificity

Highly expressed in kidney; not detectable in the other tissues tested.

Subcellular Localizations

Membrane; Multi-pass membrane protein.

Diseases

Hyperoxalaemia
Hyperoxaluria
Nephrolithiasis, Calcium Oxalate
Urolithiasis
Neonatal Abstinence Syndrome
Disease Of Adrenal Medulla
Essential Hypertension
Congenital Abnormality
Drug-induced Liver Injury
Malignant Neoplasm Of Breast
Osteochondrodysplasias
Liver Damage

Acute Lymphocytic Leukemia
Hypertensive Disease
Malignant Neoplasms
Leukemia
5,10-methylenetetrahydrofolate Reductase Deficiency
Dwarfism
Lymphoma

Pathways

Transport
Sulfate Transport
Localization
Excretion
Cell Growth
Oxalate Transport

PTMs

Sulphation

Carboxylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC13A1

References

PMID: 11161786 by Lee A., et al. The human renal sodium sulfate cotransporter (SLC13A1; hNaSi-1) cDNA and gene: organization, chromosomal localization, and functional characterization.