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Thermo Fisher Scientific SLC22A17 Monoclonal Antibody (OTI2D6), TrueMAB
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Thermo Fisher Scientific SLC22A17 Monoclonal Antibody (OTI2D6), TrueMAB

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SLC22A17 단백질을 인식하는 Mouse monoclonal antibody로, WB와 IHC(P)에서 1:500 희석으로 사용 가능. Human, Mouse, Rat 반응성. Lyophilized 형태로 제공되며, PBS buffer에 trehalose 포함. 연구용으로만 사용.

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마지막 업데이트 2025. 08. 04. 오후 06:52
Thermo Fisher Scientific CF810195 SLC22A17 Monoclonal Antibody (OTI2D6), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC22A17 Monoclonal Antibody (OTI2D6), TrueMAB

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500
Immunohistochemistry (Paraffin) (IHC (P)) 1:500

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI2D6
Immunogen Human recombinant protein fragment corresponding to amino acids 241–300 of human SLC22A17 produced in E. coli
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (recommended: Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).

Target Information

The Slc22 family of organic anion and cation transporters (OATs, OCTs, OCTNs) are transmembrane proteins mainly expressed in kidney and liver.
They contain 12 predicted alpha-helical transmembrane domains and a large extracellular loop between TMDs 1 and 2.
Members of the SLC22 family function as:

  • Uniporters mediating facilitated diffusion (OCTs)
  • Anion exchangers (OAT1, OAT3, URAT1)
  • Na(+)/L-carnitine cotransporters (OCTN2)

These transporters are involved in the absorption and excretion of drugs, xenobiotics, and endogenous compounds in intestine, liver, and kidney, playing homeostatic roles in brain and heart.
Mutations in SLC22 family genes may lead to diseases such as primary systemic carnitine deficiency or idiopathic renal hypouricemia, and can affect drug absorption or excretion.
Recent studies show SLC22A17 (receptor for Lipocalin 2) is highly expressed in hematopoietic stem cells.


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

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