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Thermo Fisher Scientific MPP10 Polyclonal Antibody
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Thermo Fisher Scientific MPP10 Polyclonal Antibody

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Rabbit polyclonal antibody targeting human MPP10 protein. Validated for IHC(P) and ICC/IF applications. High specificity with recombinant immunogen and affinity-purified for reliable research results. Suitable for nucleolar protein localization and rib...

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마지막 업데이트 2025. 07. 29. 오전 12:00
Thermo Fisher Scientific PA557134 MPP10 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific MPP10 Polyclonal Antibody

Applications

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:500
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Property Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human MPP10. Recombinant protein control fragment (Product #RP-102647)
Conjugate Unconjugated
Form Liquid
Concentration 0.3 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_2644078

Product Specific Information

Immunogen sequence:
RLTLDHEKSK LSLAEIYEQE YIKLNQQKTA EEENPEHVEI QKMMDSLFLK LDALSNFHFI PKPPVPEIKV VSNLPAITME EVAPVSVSDA ALLA

Highest antigen sequence identity to the following orthologs:

  • Mouse: 97%
  • Rat: 97%

Target Information

MPP10 (M-phase phosphoprotein 10), also known as MPHOSPH10, is a 681 amino acid protein that localizes to the fibrillar region of the nucleolus. It is phosphorylated in the M phase of the cell cycle and forms part of the 60–80S U3 small nucleolar ribonucleoprotein (U3 snoRNP) complex, essential for early cleavages during pre-18S rRNA processing. MPP10 interacts with IMP-3 and IMP-4 to form a heterotrimeric complex required for nucleolar association. The MPP10 gene is located on human chromosome 2, which contains over 500 genes. Mutations in genes on chromosome 22 are linked to disorders such as Phelan-McDermid syndrome, Neurofibromatosis type 2, autism, and schizophrenia.

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

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