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Thermo Fisher Scientific ZPR1 Recombinant Rabbit Monoclonal Antibody (10V1A2)
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Thermo Fisher Scientific ZPR1 Recombinant Rabbit Monoclonal Antibody (10V1A2)

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ZPR1 단백질을 인식하는 재조합 토끼 단클론 항체로, Western blot, IHC, ELISA에 적합합니다. 인간 및 생쥐 시료에 반응하며, HEK293 세포에서 발현되었습니다. 고순도 친화 크로마토그래피 정제 제품으로, 연구용으로만 사용 가능합니다.

카탈로그번호
MA542670
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오후 12:10
Thermo Fisher Scientific MA542670 ZPR1 Recombinant Rabbit Monoclonal Antibody (10V1A2) 100 ul pk판매 단위 pk ·
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714,600원VAT 포함 786,060원

Thermo Fisher Scientific · Thermo Fisher Scientific ZPR1 Recombinant Rabbit Monoclonal Antibody (10V1A2)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 10V1A2
Immunogen A synthetic peptide corresponding to a sequence within amino acids 360–459 of human ZNF259 (O75312)
Conjugate Unconjugated
Form Liquid
Concentration 0.38 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2911811

Product Specific Information

Positive test controls include mouse brain.
The target is usually found in the following locations: Cajal body, cell projection, cytoplasm, nucleus, axon, gem, growth cone, nucleolus, and perinuclear region.

Immunogen sequence:
DIRELVTKNP FTLGDSSNPG QTERLQEFSQ KMDQIIEGNM KAHFIMDDPA GNSYLQNVYA PEDDPEMKVE RYKRTFDQNE ELGLNDMKTE GYEAGLAPQR

Target Information

The protein encoded by this gene is found in the cytoplasm of quiescent cells but translocates to the nucleolus in proliferating cells.
It interacts with survival motor neuron protein (SMN1) to enhance pre-mRNA splicing and to induce neuronal differentiation and axonal growth.
Defects in this gene or the SMN1 gene can cause spinal muscular atrophy. Two transcript variants encoding different isoforms have been found for this gene.
[Provided by RefSeq, Nov 2015]


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

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