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Thermo Fisher Scientific MRPS30 Polyclonal Antibody
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Thermo Fisher Scientific MRPS30 Polyclonal Antibody

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Human, Mouse, Rat에 반응하는 Rabbit Polyclonal 항체로 Western Blot, ICC/IF, IP에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, 순도 95% 이상. PBS/glycerol buffer에 보관하며 연구용으로 적합.

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마지막 업데이트 2025. 08. 04. 오전 03:01
Thermo Fisher Scientific PA576836 MRPS30 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific MRPS30 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunocytochemistry (ICC/IF) 1:50–1:200
Immunoprecipitation (IP) 1:50–1:200

Product Specifications

Specification Detail
Species Reactivity Human, Mouse, Rat
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant full length Human MRPS30 (UniProt ID: Q9NP92-1, amino acids 1–439)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% 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_2720563

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

Mitochondrial ribosomes consist of a large 39S subunit and a small 28S subunit, both composed of multiple mitochondrial ribosomal proteins (MRPs) encoded by nuclear genes essential for mitochondrial protein synthesis.
MRP-S30 (mitochondrial ribosomal protein S30), also known as PDCD9 (programmed cell death protein 9), is a 439 amino acid protein localized in the mitochondrion as a component of the 28S ribosomal subunit. It functions with other MRPs to mediate protein synthesis and is expressed in kidney, liver, heart, and skeletal muscle.
The gene encoding MRP-S30 maps to human chromosome 5, which spans approximately 181 million base pairs and constitutes nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.


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

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