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Thermo Fisher Scientific Uromodulin Polyclonal Antibody
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Thermo Fisher Scientific Uromodulin Polyclonal Antibody

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Thermo Fisher Scientific의 Uromodulin Polyclonal Antibody는 Mouse Uromodulin에 특이적인 Sheep 유래 IgG 항체입니다. Western blot 및 IHC(Frozen)에 사용 가능하며, 높은 특이성과 낮은 교차 반응성을 제공합니다. 연구용으로만 사용되며 안정적인 동결건조 형태로 제공됩니다.

판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 01:09
Thermo Fisher Scientific PA547706 Uromodulin Polyclonal Antibody 100 ug pk판매 단위 pk ·
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704,800원VAT 포함 775,280원

Thermo Fisher Scientific · Thermo Fisher Scientific Uromodulin Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1 µg/mL -
Immunohistochemistry (IHC) - 2 publications
Immunohistochemistry (Frozen) (IHC (F)) 5–15 µg/mL -

Product Specifications

항목 내용
Species Reactivity Mouse
Published Species Mouse
Host / Isotype Sheep / IgG
Class Polyclonal
Type Antibody
Immunogen Mouse myeloma cell line NS0-derived recombinant mouse Uromodulin (Ser24–Ala618)
Conjugate Unconjugated
Form Lyophilized
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 5% trehalose
Contains No Preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2606308

Product Specific Information

  • In direct ELISAs and Western blots, less than 5% cross-reactivity with recombinant human Uromodulin is observed.
  • Reconstitute at 0.2 mg/mL in sterile PBS.
  • Endotoxin level is <0.10 EU per 1 µg of the antibody by the LAL method.

Target Information

This gene encodes uromodulin, the most abundant protein in normal urine. Its excretion follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinositol-anchored counterpart located on the luminal surface of the loop of Henle.
Uromodulin may act as an inhibitor of calcium crystallization in renal fluids and provide defense against urinary tract infections caused by uropathogenic bacteria.
Defects in this gene are associated with autosomal dominant renal disorders such as medullary cystic kidney disease-2 (MCKD2) and familial juvenile hyperuricemic nephropathy (FJHN). These disorders are characterized by juvenile onset of hyperuricemia, gout, and progressive renal failure.
Two major transcript variants encoding the same isoform have been described.


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

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