CacheBy
Thermo Fisher Scientific MRPL32 Polyclonal Antibody
원본

Thermo Fisher Scientific MRPL32 Polyclonal Antibody

상품 한눈에 보기

Human MRPL32 단백질을 인식하는 Rabbit Polyclonal 항체로, IHC(P)에서 1:200~1:500 희석으로 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관. 미토콘드리아 리보솜 단백질 연구용으로 적합.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 04. 오후 03:42
Thermo Fisher Scientific PA561849 MRPL32 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific MRPL32 Polyclonal Antibody

Applications

Immunohistochemistry (Paraffin) [IHC (P)]

  • Tested Dilution: 1:200–1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human MRPL32. Recombinant protein control fragment (Product # RP-101180)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 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_2644139

Product Specific Information

Immunogen sequence:
RRTIEVNRCR RRNPQKLIKV KNNIDVCPEC GHLKQKHVLC AYCYEKVCKE TAEIRRQIGK QEGGPFKAPT IETVVL

  • Highest antigen sequence identity to orthologs:
    • Mouse: 83%
    • Rat: 84%

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. These MRPs are essential for mitochondrial protein synthesis.
MRP-L32 (mitochondrial ribosomal protein L32), also known as HSPC283, is a 188 amino acid protein localized in the mitochondrion as part of the 39S ribosomal subunit. It cooperates with other MRPs to mediate protein synthesis.
The gene encoding MRP-L32 is located on human chromosome 7, which contains over 1,000 genes and accounts for nearly 5% of the human genome. Mutations in genes on chromosome 7 have been associated with various disorders, including 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.

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.