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Thermo Fisher Scientific SLC16A2 Polyclonal Antibody
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Thermo Fisher Scientific SLC16A2 Polyclonal Antibody

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SLC16A2 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, 인간 및 생쥐 시료에 반응합니다. IHC 및 ICC/IF에 사용 가능하며, 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 03. 오후 04:43
Thermo Fisher Scientific PA582084 SLC16A2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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740,000원VAT 포함 814,000원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC16A2 Polyclonal Antibody

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:200–1:500

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human SLC16A2
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS, pH 7.2, with 40% 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_2789245

Product Specific Information

Immunogen sequence:
SSRNKYQPQS GSSGPSSHSP PAAMALQSQA SEEAKGPWQE ADQEQQEPVG SPEPESEPEP EPEPEPVPVP PPEPQPEPQP LPDPAPLPEL EFESERVHEP EPT

Target Information

Monocarboxylates, such as lactate and pyruvate, play an integral role in cellular metabolism. Lactic acid is produced in large quantities as a result of glycolysis, which provides the majority of ATP to cells under normal physiological conditions. However, accumulation of lactic acid leads to a decrease in intracellular pH and cessation of glycolysis. In order for glycolysis to continue at a high rate, lactic acid must be transported out of the cell. This transport process is carried out by a family of monocarboxylate transporters (MCTs), which function as proton symports and are stereoselective for L-lactate. The MCT family consists of at least eight members, MCT 1–8, which contain between 10–12 transmembrane-helical (TM) domains, with the amino and carboxy termini located in the cytoplasm. Defects in the gene encoding for MCT8, SLC16A2, can cause monocarboxylate transporter 8 deficiency (MCT8 deficiency), a defect in cellular hormone transport causing a severe form of X-linked psychomotor retardation and abnormal thyroid levels.


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

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