Thermo Fisher Scientific MPP9 Polyclonal Antibody
Thermo Fisher Scientific의 MPP9 Polyclonal Antibody는 인간 MPP9 단백질을 인식하는 토끼 IgG 항체로, IHC(P) 실험에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 액상 형태로 제공됩니다. 세포 분열 및 M-phase 관련 연구에 활용 가능합니다.
- 카탈로그번호
- PA557970
- 판매단위
- pk
카탈로그
1개 옵션 · 카탈로그 번호를 클릭하면 복사됩니다Thermo Fisher Scientific · Thermo Fisher Scientific MPP9 Polyclonal Antibody
Applications
- Immunohistochemistry (Paraffin) (IHC (P)): 1:500–1:1,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human MPP9. Recombinant protein control fragment (Product #RP-97636) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage buffer | PBS, pH 7.2, with 40% glycerol |
| Contains | 0.02% sodium azide |
| Storage conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping conditions | Wet ice |
| RRID | AB_2644085 |
Product Specific Information
Immunogen sequence:
YKSKDPKEFM EHIDVPKGQY VAPAVPAESL VDGVKNENFY IQTPEECHVS LKEDVSISPG EFEHNFLGEN KVSEVYSGKT NSNAITSWAQ KLKQNQPK
Highest antigen sequence identity to the following orthologs:
- Mouse: 56%
- Rat: 64%
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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