Slc10a7 Antibodies

AND Slc10a7 ELISA kits, Slc10a7 Proteins

Many biological assays use antibodies to detect Slc10a7, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Slc10a7 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Slc10a7 antibodies...

We validate the specificity of these antibodies to Slc10a7 by testing them on tissues known to express Slc10a7 positively and negatively. Browse below to find the Slc10a7 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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Slc10a7 Infographic by Boster Bio

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Anti-SLC10A7 Antibody

3 Q&As

Human, Mouse, Rat

ELISA, WB

$335
Cat # A07374-1
100ul

Slc10a7 Overview

Facts about Sodium/bile acid cotransporter 7.

Sodium/bile acid cotransporter 7 (Slc10a7)

Does not show transport activity towards bile acids or steroid sulfates (like taurocholate, cholate, chenodeoxycholate, estrone-3-sulfate, dehydroepiandrosterone sulfate (DHEAS) and pregnenolone sulfate). .

Gene Information

Mouse
Gene Name:	Slc10a7
Uniprot:	Q5PT53
Entrez:	76775

Family

Belongs to:

bile acid:sodium symporter (BASS) (TC 2.A.28) family

Alternative Names

C4orf13; chromosome 4 open reading frame 13; DKFZp313H0531; DKFZp566M114; DKFZp779O2438; MGC25043; Na(+)/bile acid cotransporter 7; P7; SBF-domain containing protein; sodium/bile acid cotransporter 7; solute carrier family 10 (sodium/bile acid cotransporter family), member 7; Solute carrier family 10 member 7

Molecular Weight

Mass (kDA):
37.256 kDA

Genomic Context


Mouse

Location:	8\|8 C1
Sequence:	8;

Tissue Specificity

Expressed in heart, brain, colon, lung, liver, adrenal gland, stomach and ovary. Also expressed weakly in small intestine.

Diseases

Headache
Azoospermia
Chromosomal Translocation
Primary Hypogonadism
Hypogonadism

Pathways

Transport
Localization
Secretory Pathway
Hypersensitivity

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Slc10a7

References

PMID: 17628207 by Godoy J.R., et al. Molecular and phylogenetic characterization of a novel putative membrane transporter (SLC10A7), conserved in vertebrates and bacteria.

PMID: 30082715 by Dubail J., et al. SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects.