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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 Rabbit Polyclonal 항체로, Western blot, IHC, ICC/IF, ELISA에 적합합니다. Human, Mouse, Rat 시료 반응성이 있으며, PBS/glycerol buffer에 보관됩니다. 세포골격 연구 및 MYH9 관련 질환 연구에 유용합니다.

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마지막 업데이트 2025. 08. 04. 오전 08:10
Thermo Fisher Scientific PA5120506 MYH9 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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710,700원VAT 포함 781,770원

Thermo Fisher Scientific · Thermo Fisher Scientific MYH9 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1 µg/mL

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1801–1960 of human MYH9 (NP_002464.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.79 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.09% sodium azide
Storage Conditions −20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2914078

Product Specific Information

  • Positive test controls: HeLa, HT-29, A-549, NIH/3T3, C6
  • Subcellular localization: Cytoplasm, cell cortex, cytoskeleton

Immunogen sequence:
VKSKYKASIT ALEAKIAQLE EQLDNETKER QAACKQVRRT EKKLKDVLLQ VDDERRNAEQ
YKDQADKAST RLKQLKRQLE EAEEEAQRAN ASRRKLQREL EDATETADAM NREVSSLKNK
LRRGDLPFVV PRRMARKGAG DGSDEEVDGK ADGAEAKPAE

Target Information

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

Mutations in MYH9 cause autosomal dominant MYH9-related diseases (MYH9-RD) such as May-Hegglin anomaly, Fechtner syndrome, and Epstein syndrome, often associated with macrothrombocytopenia, hearing loss, renal failure, and cataracts.
MYH9 also plays a crucial role in hematopoiesis, where its dysfunction leads to hematopoietic failure and severe cytopenia.


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

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