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Thermo Fisher Scientific MYH9 Polyclonal Antibody
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Thermo Fisher Scientific MYH9 Polyclonal Antibody

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MYH9 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal 항체. Western blot 및 Immunocytochemistry에 최적화되어 있으며, Human, Mouse, Rat에 반응. 비보존제 액상 형태로 -20°C에서 보관. MYH9 관련 질환 연구에 적합.

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마지막 업데이트 2025. 08. 03. 오후 03:26
Thermo Fisher Scientific PA517025 MYH9 Polyclonal Antibody 100 ul pk판매 단위 pk
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629,600원VAT 포함 692,560원

Thermo Fisher Scientific · Thermo Fisher Scientific MYH9 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:1,000 View 2 publications
Immunocytochemistry (ICC/IF) 1:50 View 2 publications

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Dog, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to the carboxy terminus of mouse myosin IIa
Conjugate Unconjugated
Form Liquid
Concentration 20 µg/mL
Purification Affinity chromatography
Storage Buffer 0.01M HEPES (pH 7.5), 0.15M NaCl, 100 µg/mL BSA, 50% glycerol
Contains No preservative
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_10984569

Product Specific Information

  • It is not recommended to aliquot this antibody.
  • This antibody is not cross-reactive with the nonmuscle heavy chains of myosin IIb or IIc.

Target Information

The MYH9 gene, located on chromosome 22q12.3, encodes the heavy chain of non-muscle myosin IIA (NMHC IIA), a critical component of the actin cytoskeleton involved in cell migration, adhesion, division, and shape maintenance.
It spans over 106 kilobases and includes 41 exons encoding a 1,960 amino acid protein that forms a hexameric complex with two heavy chains, two regulatory light chains, and two essential light chains.

Mutations in MYH9 cause autosomal dominant disorders known as MYH9-related diseases (MYH9-RD), including May-Hegglin anomaly, Fechtner syndrome, and Epstein syndrome, characterized by macrothrombocytopenia and sometimes hearing loss, renal failure, and cataracts.
MYH9 function is essential for hematopoietic stem and progenitor cell maintenance; its loss leads to blood cell deficiencies and bone marrow failure.


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

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