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SLC6A8 Recombinant monoclonal antibody

SLC6A8 Uni-rAb® Recombinant Antibody for WB, ELISA
Cat No. 88049-1-RR

产品说明书

CloneNo. 260302B8

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat

应用

WB, ELISA

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

缓冲液配方:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
PBS Only
偶联物:  Unconjugated
Unconjugated
规格价格库存


经过测试的应用

Positive WB detected inrat kidney tissue, mouse heart tissue, mouse kidney tissue, rat heart tissue

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:2000-1:10000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

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

经测试应用 WB, ELISA Application Description
经测试反应性 human, mouse, rat
免疫原

CatNo: Ag14500

Product name: Recombinant human SLC6A8 protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 541-635 aa of BC012355

Sequence: YYEPLVYNNTYVYPWWGEAMGWAFALSSMLCVPLHLLGCLLRAKGTMAERWQHLTQPIWGLHHLEYRAQDADVRGLTTLTPVSESSKVVVVESVM

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Recombinant
产品类型 Antibody
全称 solute carrier family 6 (neurotransmitter transporter, creatine), member 8
别名 Creatine transporter 1, CRT, CRTR, CT1, Sodium- and chloride-dependent creatine transporter 1
计算分子量 635 aa, 71 kDa
观测分子量 65-75 kDa
GenBank蛋白编号BC012355
基因名称 SLC6A8
Gene ID (NCBI) 6535
偶联类型 Unconjugated
形式Liquid
纯化方式Protein A purification
UNIPROT IDP48029
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

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.

实验方案

Product Specific Protocols
WB protocol for SLC6A8 antibody 88049-1-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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