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Thermo Fisher Scientific SLC22A4 Polyclonal Antibody
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Thermo Fisher Scientific SLC22A4 Polyclonal Antibody

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SLC22A4 단백질을 인식하는 Rabbit Polyclonal Antibody로, Western Blot에 적합합니다. Human, Mouse, Rat에 반응하며, 항원 친화 크로마토그래피로 정제되었습니다. 고순도(>95%)의 액상 형태로, 장기 보관 시 -20°C에서 보관 권장됩니다.

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마지막 업데이트 2025. 08. 01. 오후 01:19
Thermo Fisher Scientific PA575776 SLC22A4 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC22A4 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues in Human SLC22A4
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2719504

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

Carnitine (b-hydroxy-g-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.
The gene encoding human OCTN1 maps to chromosome 5 and the gene encoding human OCTN2 maps to chromosome 5q31. 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.

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