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Thermo Fisher Scientific MYH9 Monoclonal Antibody (GT218)
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Thermo Fisher Scientific MYH9 Monoclonal Antibody (GT218)

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MYH9 단백질을 표적으로 하는 Thermo Fisher Scientific의 GT218 단클론 항체로, Western blot, IHC, Flow cytometry 등에 적합. 인간 및 마우스 반응성, Protein A로 정제된 액상 형태. 세포골격 연구 및 MYH9 관련 질환 연구용.

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마지막 업데이트 2025. 08. 04. 오후 03:54
Thermo Fisher Scientific MA527765 MYH9 Monoclonal Antibody (GT218) 100 ul pk판매 단위 pk ·
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731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific MYH9 Monoclonal Antibody (GT218)

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:3,000 View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000 -
Flow Cytometry (Flow) 1:100–1:1,000 -

Product Specifications

Specification Description
Species Reactivity Human, Mouse
Published Species Dog
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone GT218
Immunogen Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7, with 20% glycerol
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2735282

Product Specific Information

  • Positive Control: A431
  • Predicted Reactivity: Rat (97%), Xenopus laevis (89%), Dog (99%), Chicken (94%), Bovine (99%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

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.
MYH9 spans over 106 kilobases and includes 41 exons, encoding a 1,960 amino acid protein that forms a hexameric complex with 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 potential hearing loss, renal failure, or cataracts.
MYH9 also plays a vital role in hematopoiesis, essential for hematopoietic stem and progenitor cell maintenance; its loss leads to severe 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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