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Thermo Fisher Scientific P2X2 Polyclonal Antibody
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Thermo Fisher Scientific P2X2 Polyclonal Antibody

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P2X2 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot, IHC, Flow cytometry에 적합하며 인간, 마우스, 랫트 반응성. 고순도 친화 크로마토그래피 정제, 액상 형태로 안정적 보관 가능.

카탈로그번호
PA5119683
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 12:08
Thermo Fisher Scientific PA5119683 P2X2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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710,700원VAT 포함 781,770원

Thermo Fisher Scientific · Thermo Fisher Scientific P2X2 Polyclonal Antibody

Thermo Fisher Scientific P2X2 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:1,000 View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200 -
Flow Cytometry (Flow) 1:50–1:100 -

Product Specifications

Item Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide within C-terminal human P2X2
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol, 0.2% BSA
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term. For long term, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2913256

Product Specific Information

  • Positive Control: Mouse brain tissue lysates, rat brain tissue, human esophagus tissue, MCF-7
  • Subcellular Location: Cell membrane

Target Information

P2rx2 belongs to the ligand-gated ion channel family activated by extracellular ATP. Each receptor is composed of a trimer of subunits (P2X1–7) sharing two transmembrane domains. P2rx2 mediates synaptic transmission between neurons and smooth muscle, playing roles in sensory neuron responses, neuromuscular junction formation, hearing, taste perception, and peristalsis.

In the inner ear, P2rx2 is involved in sound transduction, auditory neurotransmission, outer hair cell electromotility, inner ear gap junctions, and K⁺ recycling. Mutations in P2RX2 are associated with autosomal dominant deafness (DFNA41).


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

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