CacheBy
Thermo Fisher Scientific SLC22A5 Polyclonal Antibody
원본

Thermo Fisher Scientific SLC22A5 Polyclonal Antibody

상품 한눈에 보기

SLC22A5 단백질을 인식하는 Rabbit Polyclonal 항체로, WB, IHC, ICC/IF에 적합합니다. Human, Mouse, Rat에서 반응하며, 고순도 Affinity chromatography로 정제되었습니다. -20°C에서 보관하며 연구용으로 사용됩니다.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
ADRepligen 웨비나PATsmart를 활용한 바이오공정 분석 전략 · 10/7 오전 10시자세히보기
Thermo Fisher Scientific PA5102460 SLC22A5 Polyclonal Antibody 100 ul pk판매 단위 pk
재고 확인 필요
627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC22A5 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:100–1:500

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human SLC22A5 (Accession O76082), corresponding to amino acid residues M445–M495
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions –20°C
Shipping Conditions Wet ice
RRID AB_2851864

Product Specific Information

Antibody detects endogenous levels of total SLC22A5.

Target Information

Carnitine (β-hydroxy-γ-trimethylaminobutyrate) is a small, highly polar compound that aids in the β-oxidation of long-chain fatty acids. Organic cation/carnitine transporters (OCTN) assist in the elimination of cationic compounds, including xenobiotics, and transport carnitine for reabsorption in the kidney. Similar to organic cation transporters (OCT), OCTN proteins localize to the plasma membrane of epithelial cells.
OCTN1 is expressed in kidney, trachea, bone marrow, and fetal liver. OCTN2 is abundantly expressed in kidney, skeletal muscle, placenta, and heart. OCTN3 is strongly expressed in testis and weakly in kidney.
Mutations in the gene encoding OCTN2 lead to systemic carnitine deficiency (SCD), an autosomal recessive disorder characterized by cardiomyopathy, skeletal myopathy, lethargy, hypoglycemia, and hyperammonemia.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0개

아직 등록된 문의가 없어요.