SLC23A2 Antibodies

AND SLC23A2 ELISA kits, SLC23A2 Proteins

Many biological assays use antibodies to detect SLC23A2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC23A2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC23A2 antibodies...

We validate the specificity of these antibodies to SLC23A2 by testing them on tissues known to express SLC23A2 positively and negatively. Browse below to find the SLC23A2 antibody that suites your experiment. We have 1 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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SLC23A2 Infographic by Boster Bio

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SLC23A2 (NM_005116) Human Over-expression Lysate

Human

$960
Cat # LS009962
100 µg

SLC23A2 Overview

Facts about Solute carrier family 23 member 2.

SLC23A2 3D structure. Source: alphafold

Solute carrier family 23 member 2 (SLC23A2)

Sodium/ascorbate cotransporter. Mediates electrogenic uptake of vitamin C, with a stoichiometry of 2 Na(+) for each ascorbate.

Gene Information

Human
Gene Name:	SLC23A2
Uniprot:	Q9UGH3
Entrez:	9962

Family

Belongs to:

xanthine/uracil permease family

Alternative Names

KIAA0238SLC23A1; Na(+)/L-ascorbic acid transporter 2; Nucleobase transporter-like 1 protein; Sodium-dependent vitamin C transporter 2; sodium-dependent vitamin C transporter-2; solute carrier family 23 (nucleobase transporters), member 1; solute carrier family 23 (nucleobase transporters), member 2; solute carrier family 23 member 2; SVCT2NBTL1; Yolk sac permease-like molecule 2; YSPL2hSVCT2

Molecular Weight

Mass (kDA):
70.337 kDA

Genomic Context


Human

Location:	20p13
Sequence:	20; NC_000020.11 (4852358..5010313, complement)

Tissue Specificity

Ubiquitous.

Subcellular Localizations

Cell membrane; Multi-pass membrane protein.

Diseases

Nervousness
Malignant Neoplasms
Neoplasms
Choriocarcinoma
Atherosclerosis
Ischemia
Neurodegenerative Disorders
Disease Of Adrenal Medulla
Hemorrhage
Cerebrovascular Accident
Brain Neoplasms
Melanoma

Hypoxia
Arterial Occlusion
Occlusion, Middle Cerebral Artery
Cardiovascular Diseases
Infarction, Middle Cerebral Artery
Cerebral Artery Occlusion
Neuroblastoma

Pathways

Transport
Localization
Osteoblast Differentiation
Aging
Pathogenesis
Excretion
Myelination
Translation
Senescence
L-ascorbic Acid Transport
Rna Interference
Secretion
Protein Targeting

Brain Development
Cytokine Secretion
Pigmentation
Platelet Activation
Intestinal Absorption
Transepithelial Transport
Response To Oxidative Stress

PTMs

Oxidation
Phosphorylation
Reduction

Demethylation
Carboxylation
Cleavage

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC23A2

References

PMID: 9804989 by Faaland C.A., et al. Molecular characterization of two novel transporters from human and mouse kidney and from LLC-PK1 cells reveals a novel conserved family that is homologous to bacterial and Aspergillus nucleobase transporters.

PMID: 10471399 by Rajan D.P., et al. Human placental sodium-dependent vitamin C transporter (SVCT2): molecular cloning and transport function.