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Thermo Fisher Scientific PPP2R2B Polyclonal Antibody
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Thermo Fisher Scientific PPP2R2B Polyclonal Antibody

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PPP2R2B 단백질 인식용 Rabbit Polyclonal 항체로 Western blot, IHC, Flow Cytometry에 적합합니다. Protein A 및 항원 친화 크로마토그래피로 정제되었으며, 인간 시료에 반응합니다. 연구용으로 세포 성장 조절 관련 연구에 활용 가능합니다.

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마지막 업데이트 2025. 08. 04. 오후 06:40
Thermo Fisher Scientific PA572539 PPP2R2B Polyclonal Antibody 400 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific PPP2R2B Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:100
Flow Cytometry (Flow) 1:10–1:50

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH conjugated synthetic peptide between 104–130 amino acids from the central region of human PPP2R2B
Conjugate Unconjugated
Form Liquid
Concentration 0.45 mg/mL
Purification Protein A, Antigen affinity chromatography
Storage Buffer PBS, pH 7.4
Contains 0.09% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2718393

Target Information

The product of this gene belongs to the phosphatase 2 regulatory subunit B family. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases and is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme composed of a catalytic subunit and a constant regulatory subunit, which associates with various regulatory subunits. The B regulatory subunit may modulate substrate selectivity and catalytic activity.

This gene encodes a beta isoform of the regulatory subunit B55 subfamily. Defects in this gene cause autosomal dominant spinocerebellar ataxia 12 (SCA12), a disease associated with cerebellar degeneration, sometimes involving the brainstem and spinal cord, resulting in poor coordination of speech and body movements. Multiple alternatively spliced variants encoding different isoforms have been identified for this gene. The 5′ UTR of some variants includes a CAG trinucleotide repeat sequence (7–28 copies) that can expand to 66–78 copies in cases of SCA12.

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

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