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Thermo Fisher Scientific SLC6A15 Polyclonal Antibody
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Thermo Fisher Scientific SLC6A15 Polyclonal Antibody

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SLC6A15 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체로, Western blot 및 Immunoprecipitation에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 인간에 반응하며 마우스·랫·소·오랑우탄에도 예측 반응합니다.

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마지막 업데이트 2025. 08. 02. 오후 07:32
Thermo Fisher Scientific A304476AT SLC6A15 Polyclonal Antibody 10 ul pk판매 단위 pk ·
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194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC6A15 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:1,000–1:5,000
Immunoprecipitation (IP) 2–10 µg/mg lysate

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 653–703 of Human Solute Carrier Family 6 (neutral amino acid transporter), Member 15
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage buffer Phosphate/tris citrate, pH 7–8
Contains 0.09% sodium azide
Storage conditions 4°C
Shipping conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • Based on 100% sequence identity, this antibody is predicted to react with Mouse, Rat, Bovine, and Orangutan.

Target Information

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 SBAT1, is a 730 amino acid multi-pass membrane protein functioning as a sodium-dependent neutral amino acid transporter.
It belongs to the sodium neurotransmitter symporter (SNF) family and SLC6A15 subfamily, differing from other members by not being chloride-dependent.
SLC6A15 is expressed in the brain and encoded by a gene on human chromosome 12, which contains over 1,100 genes and accounts for approximately 4.5% of the human genome.
Chromosome 12 is linked to various disorders such as hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome, and trisomy 12p, which can cause facial developmental defects and seizure disorders.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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