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Thermo Fisher Scientific MOB3A/MOB3B Polyclonal Antibody
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Thermo Fisher Scientific MOB3A/MOB3B Polyclonal Antibody

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MOB3A/MOB3B 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체로, Western blot에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 고순도(>95%)를 보장합니다. Human, Mouse, Rat 시료에 반응하며, 장기 보관 시 -20°C에서 안정적입니다.

카탈로그번호
PA575725
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 08:41
Thermo Fisher Scientific PA575725 MOB3A/MOB3B Polyclonal Antibody 100 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific MOB3A/MOB3B Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues in Human MOB3A/MOB3B
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_2719453

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 confirmed by SDS-PAGE.

Target Information

MOBKL2A (Mps one binder kinase activator-like 2A), also known as MOB-LAK or MOB3A, is a 217-amino-acid protein that regulates kinase activity. It belongs to the MOB1/phocein family and is encoded by a gene located on human chromosome 19.
Chromosome 19 spans approximately 63 million bases and contains over 1,400 genes, accounting for more than 2% of the human genome. It has one of the highest gene densities among human chromosomes and includes genes for immunoglobulin superfamily members such as killer cell and leukocyte Ig-like receptors, ICAMs, CEACAM, PSG families, and Fcα receptors.
Additionally, genes influencing eye and hair color, as well as those associated with Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, CADASIL, hypercholesterolemia, and insulin-dependent diabetes, are located on chromosome 19.


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

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