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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 및 Rat 시료에 반응하는 MRPS30 단백질에 대한 Rabbit Polyclonal Antibody. Western blot 및 파라핀 포매 조직면역염색에 적합. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 05. 오전 08:24
Thermo Fisher Scientific PA554337 MRPS30 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific MRPS30 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human MRPS30. Recombinant protein control fragment (Product #RP-92026).
Conjugate Unconjugated
Form Liquid
Concentration 0.05 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_2644195

Product Specific Information

Immunogen sequence:
FAWTGAQAMY QGFWSEADVT RPFVSQAVIT DGKYFSFFCY QLNTLALTTQ ADQNNPRKNI CWGTQSKPLY ETIEDNDVKG FNDDVLLQIV HFLLNRP

Antigen sequence identity:

  • Mouse: 91%
  • Rat: 94%

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 part of the 28S ribosomal subunit. It functions with other MRPs to mediate mitochondrial protein synthesis.
MRP-S30 is expressed in kidney, liver, heart, and skeletal muscle. The MRPS30 gene maps to human chromosome 5, which contains 181 million base pairs and represents nearly 6% of the human genome. Deletion of the p arm of chromosome 5 causes Cri du chat syndrome, while deletion of the q arm or the entire 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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