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Thermo Fisher Scientific MRPL32 Polyclonal Antibody
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Thermo Fisher Scientific MRPL32 Polyclonal Antibody

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MRPL32 단백질을 인식하는 Rabbit Polyclonal 항체로, Human 및 Mouse 시료에 반응합니다. Western blot, ICC/IF, ELISA에 적합하며, 고순도의 Affinity Chromatography 정제 제품입니다. PBS/glycerol buffer에 보관하며 연구용으로 사용됩니다.

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마지막 업데이트 2025. 08. 04. 오후 01:47
Thermo Fisher Scientific PA5109980 MRPL32 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific MRPL32 Polyclonal Antibody

Applications and Tested Dilution

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

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 19–188 of human MRPL32 (NP_114109.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.78 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2855391

Product Specific Information

Immunogen sequence:
VLRNYWERLL RKLPQSRPGF PSPPWGPALA VQGPAMFTEP ANDTSGSKEN SSLLDSIFWM AAPKNRRTIE VNRCRRRNPQ KLIKVKNNID VCPECGHLKQ KHVLCAYCYE KVCKETAEIR RQIGKQEGGP FKAPTIETVV LYTGETPSEQ DQGKRIIERD RKRPSWFTQN

Target Information

Mitochondrial ribosomes consist of a large 39S subunit and a small 28S subunit, both of which are comprised of multiple mitochondrial ribosomal proteins (MRPs) that are encoded by nuclear genes and are essential for protein synthesis within mitochondria.
MRP-L32 (mitochondrial ribosomal protein L32), also known as HSPC283, is a 188 amino acid protein that localizes to the mitochondrion, where it exists as a component of the 39S ribosomal subunit and works in conjunction with other MRPs to mediate protein synthesis.
The gene encoding MRP-L32 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia, and Shwachman-Diamond syndrome.


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

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