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

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MPP9 단백질을 인식하는 Rabbit Polyclonal 항체로, WB, IHC, ICC, ELISA 등 다양한 응용에 적합합니다. Human, Mouse, Rat 시료에 반응하며, Protein A로 정제된 1 mg/mL 액상 형태입니다. 연구용으로 세포주기 관련 단백질 분석에 활용됩니다.

카탈로그번호
BS-7812R
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오후 05:48
Thermo Fisher Scientific BS-7812R MPP9 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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531,800원VAT 포함 584,980원

Thermo Fisher Scientific · Thermo Fisher Scientific MPP9 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC-P) 1:100–1:500
Immunohistochemistry (Frozen) (IHC-F) 1:100–1:500
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1:500–1:1,000

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH-conjugated synthetic peptide derived from human MPP9/MPHOSPH9 (amino acids 451–550)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer 0.01M TBS, pH 7.4, with 50% glycerol, 1% BSA
Contains 0.02% ProClin 300
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)

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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