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Thermo Fisher Scientific Phospho-Synapsin 1 (Ser9) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-Synapsin 1 (Ser9) Polyclonal Antibody

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Synapsin 1의 Ser9 위치에서 인산화된 형태를 특이적으로 검출하는 rabbit polyclonal antibody. WB, IHC, ICC/IF 등 다양한 응용에 적합. 인간, 마우스, 랫트 반응성. 고순도 정제 및 안정적 저장 조건 제공.

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마지막 업데이트 2025. 08. 02. 오전 10:45
Thermo Fisher Scientific PA5104822 Phospho-Synapsin 1 (Ser9) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-Synapsin 1 (Ser9) Polyclonal Antibody

Thermo Fisher Scientific Phospho-Synapsin 1 (Ser9) Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:100–1:500

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human SYN1 (Accession P17600), corresponding to amino acid residues around phosphorylated Ser9
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Sequential chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2816295

Product Specific Information

Antibody detects endogenous levels of Synapsin I only when phosphorylated at Serine 9.

Target Information

SYN1 (synapsin 1) is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins that associate with the cytoplasmic surface of synaptic vesicles. Family members share common protein domains and are implicated in synaptogenesis and modulation of neurotransmitter release, suggesting a role in neuropsychiatric diseases. Synapsin 1 regulates axonogenesis and synaptogenesis, serving as a substrate for various protein kinases. Phosphorylation may regulate its function in nerve terminals. Mutations in this gene can be associated with X-linked neuronal degenerative disorders such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.

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

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