Slc16a12 Antibodies

AND Slc16a12 ELISA kits, Slc16a12 Proteins

Many biological assays use antibodies to detect Slc16a12, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Slc16a12 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Slc16a12 antibodies...

We validate the specificity of these antibodies to Slc16a12 by testing them on tissues known to express Slc16a12 positively and negatively. Browse below to find the Slc16a12 antibody that suites your experiment. We have 2 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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Slc16a12 Infographic by Boster Bio

All Slc16a12 Products

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Product

Figures

Specificity

Applications

Price

Anti-MOT12 SLC16A12 Antibody

6 Q&As

Human, Mouse

ELISA, IHC-P, WB, IF (paraffin)

$335
Cat # A11725
100ul

Anti-MCT12 SLC16A12 Antibody

Human, Mouse

ELISA, IHC, WB

$380
Cat # A11725-1
100ul

Slc16a12 Overview

Facts about Monocarboxylate transporter 12.

Monocarboxylate transporter 12 (Slc16a12)

Proton-linked monocarboxylate transporter that mediates creatine transport across the plasma membrane. .

Gene Information

Mouse
Gene Name:	Slc16a12
Uniprot:	Q8BGC3
Entrez:	240638

Family

Belongs to:

major facilitator superfamily

Alternative Names

CJMG; DKFZp686E188; MCT 12; MCT12; MCT12monocarboxylate transporter 12; SLC16A12; solute carrier family 16 (monocarboxylic acid transporters), member 12; Solute carrier family 16 member 12; solute carrier family 16, member 12 (monocarboxylic acid transporter 12)

Molecular Weight

Mass (kDA):
53.152 kDA

Genomic Context


Mouse

Location:	19\|19 C1
Sequence:	19;

Diseases

Juvenile Cataract
Cataract
Senile Cataract
Malnutrition
Malignant Neoplasm Of Breast
Colonic Neoplasms
Malignant Tumor Of Colon
Oculocutaneous Albinism Type 2
Malignant Neoplasms
Neoplasms
Hyperglycemia
Mammary Neoplasms

Riboflavin Deficiency
Malignant Neoplasm Of Prostate
Keratitis
Right-sided Displacement Of Abomasum
Haploinsufficiency
Albinism, Oculocutaneous
Corneal Diseases

Pathways

Transport
Methylation
Dna Hypermethylation
Riboflavin Transport

PTMs

Carboxylation

Methylation

Oxidation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Slc16a12

References

PMID: 21778275 by Castorino J.J., et al. Juvenile cataract-associated mutation of solute carrier SLC16A12 impairs trafficking of the protein to the plasma membrane.