CacheBy
Thermo Fisher Scientific SLC6A15 Polyclonal Antibody
원본

Thermo Fisher Scientific SLC6A15 Polyclonal Antibody

상품 한눈에 보기

Thermo Fisher Scientific의 SLC6A15 폴리클로날 항체는 인간 SLC6A15 단백질(653–703aa)에 특이적입니다. WB 및 IP에 적합하며, 항원 친화 크로마토그래피로 정제된 액상 형태입니다. 인간, 마우스, 랫, 보바인, 오랑우탄에 반응 예측되며 연구용으로 사용됩니다.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 01. 오후 06:19
Thermo Fisher Scientific A304476A SLC6A15 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
658,900원VAT 포함 724,790원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC6A15 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:1,000–1:5,000

Immunoprecipitation (IP)

  • Tested Dilution: 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 to 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, 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 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 in that it does not appear to be chloride-dependent.
SLC6A15 is expressed in brain and 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.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.