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Bethyl Laboratories
SLC6A15 Polyclonal Antibody
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SLC6A15 Antibody (A304-475A) in WB
Detection of human SLC6A15 by western blot. Samples: Whole cell lysate (50 µg) from HeLa, HEK293T, and Jurkat cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-SLC6A15 antibody (Product # A304-475A) (lot A304-475A-1) used for WB at 0.1 µg/mL. Detection: Chemiluminescence with an exposure time of 3 minutes.
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
产品信息
A304-475A
产品规格
种属反应
Human
宿主/亚型
Rabbit
/ IgG
分类
Polyclonal
类型
Antibody
抗原
Region between residue 650 to 700 of Human Solute Carrier Family 6 (neutral amino acid transporter), Member 15.
偶联物
Unconjugated
Unconjugated
Unconjugated
形式
Liquid
浓度
1 mg/mL
规格
100 µg
纯化类型
Antigen affinity chromatography
保存液
phosphate/tris citrate, pH 7-8
内含物
0.09% sodium azide
保存条件
4°C
运输条件
Ambient (domestic); Wet ice (international)
产品详细信息
The recommended shelf life for this product is 1 year from date of receipt.
靶标信息
SLC6A15 (solute carrier family 6 (neutral amino acid transporter), member 15), also known as sodium-dependent neutral amino acid transporter B(0)AT2, transporter v7-3, NTT73 or sodium-coupled branched-chain amino-acid transporter 1 (SBAT1), is a 730 amino acid multi-pass membrane protein that acts as a sodium-dependent neutral amino acid transporter. A member of the sodium neurotransmitter symporter (SNF) family and SLC6A15 subfamily, SLC6A15 differs from other members of its family in that it does not appear to be chloride-dependent. SLC6A15 is expressed in brain and is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4. 5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
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生物信息学
蛋白别名: homolog of rat orphan transporter v7-3; orphan sodium- and chloride-dependent neurotransmitter transporter NTT73; orphan transporter v7-3; sodium- and chloride-dependent neurotransmitter transporter NTT73; sodium-coupled branched-chain amino-acid transporter 1; sodium/chloride dependent neurotransmitter transporter Homo sapiens orphan neurotransmitter transporter NTT7; solute carrier family 6 (neurotransmitter transporter), member 15; solute carrier family 6 (neutral amino acid transporter), member 15; transporter v7-3; unnamed protein product
基因别名: hv7-3; NTT73; SBAT1; V7-3
UniProt ID: (Human) Q9H2J7
Entrez Gene ID: (Human) 55117
neutral amino acid:sodium symporter activity
proline:sodium symporter activity
neurotransmitter transporter activity
protein binding
amino acid transmembrane transporter activity
alanine:sodium symporter activity
branched-chain amino acid:sodium symporter activity
transmembrane transporter activity
L-asparagine:sodium symporter activity
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