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Thermo Fisher Scientific MPP9 Polyclonal Antibody
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Thermo Fisher Scientific MPP9 Polyclonal Antibody

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Human MPP9 단백질을 인식하는 Rabbit Polyclonal Antibody로, Western blot과 Immunocytochemistry에 적합합니다. 합성 펩타이드 면역원으로 제작되었으며, 액상 형태로 1 mg/mL 농도입니다. -20°C에서 보관하며 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 05. 오전 09:29
Thermo Fisher Scientific PA5101677 MPP9 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific MPP9 Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunocytochemistry (ICC/IF) 1:100–1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human MPHOSPH9 (Accession Q99550), corresponding to amino acid residues H449–V499
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2851111

Product Specific Information

Antibody detects endogenous levels of total MPHOSPH9.

Target Information

Progression of cells from interphase to mitosis involves alterations in cell structures and activities. The transition from G2 to M phase is induced by M phase-promoting factor (MPF). In M phase, many proteins are phosphorylated directly by MPF or indirectly by kinases activated by MPF. These M phase phosphoproteins (MPPs), also known as MPHOSPHs, permit disassembly of interphase structures and generation of M phase enzymatic activities and structures.

MPP9 (M-phase phosphoprotein 9), also known as MPHOSPH9, is a 1,031 amino acid peripheral membrane protein of the Golgi apparatus that exists as two alternatively spliced isoforms. The gene encoding MPP9 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome, and trisomy 12p.

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

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