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SLC6A8 Recombinant monoclonal antibody, PBS Only

SLC6A8 Uni-rAb® Recombinant Antibody for WB, Indirect ELISA

Cat No. 88049-1-PBS
Clone No.260302B8

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, Indirect ELISA

Creatine transporter 1, CRT, CRTR, CT1, Sodium- and chloride-dependent creatine transporter 1

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 
SKU: 

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Product Information

88049-1-PBS targets SLC6A8 in WB, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen

CatNo: Ag14500

Product name: Recombinant human SLC6A8 protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 541-635 aa of BC012355

Sequence: YYEPLVYNNTYVYPWWGEAMGWAFALSSMLCVPLHLLGCLLRAKGTMAERWQHLTQPIWGLHHLEYRAQDADVRGLTTLTPVSESSKVVVVESVM

Predict reactive species
Full Name solute carrier family 6 (neurotransmitter transporter, creatine), member 8
Calculated Molecular Weight 635 aa, 71 kDa
Observed Molecular Weight 65-75 kDa
GenBank Accession NumberBC012355
Gene Symbol SLC6A8
Gene ID (NCBI) 6535
Conjugate Unconjugated
FormLiquid
Purification MethodProtein A purification
UNIPROT IDP48029
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

SLC6A8, also known as the sodium- and chloride-dependent creatine transporter 1 (CT1), plays a critical role in transporting creatine, a crucial molecule for energy metabolism, into cells. SLC6A8 belongs to the solute carrier family 6 (SLC6), responsible for transporting diverse molecules across cell membranes. SLC6A8 expression is highest in muscle, kidney, and other tissues with high energy demands. Mutations in SLC6A8 cause creatine transporter deficiency, an X-linked mental retardation disorder (PMID: 17465020). The 75 kDa band is a glycosylated modified form.

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