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Thermo Fisher Scientific SCN9A Polyclonal Antibody
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Thermo Fisher Scientific SCN9A Polyclonal Antibody

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SCN9A 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체로, 인간 시료에 반응합니다. IHC(P)에서 10 µg/mL 농도로 사용되며, 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용되며 SCN9A/Nav1.7 단백질 연구에 적합합니다.

카탈로그번호
PA534191
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 12:49
Thermo Fisher Scientific PA534191 SCN9A Polyclonal Antibody 50 ug pk판매 단위 pk ·
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699,000원VAT 포함 768,900원

Thermo Fisher Scientific · Thermo Fisher Scientific SCN9A Polyclonal Antibody

Thermo Fisher Scientific SCN9A Polyclonal Antibody

Applications and Tested Dilution

  • Immunohistochemistry (Paraffin) [IHC (P)]: 10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic 17 amino acid peptide from internal region of human SCN9A / Nav1.7
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS
Contains 0.1% 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_2551544

Product Specific Information

Percent identity with other species by BLAST analysis:
Human, Gorilla, Gibbon, Monkey (100%); Marmoset, Mouse, Panda, Dog, Bovine, Horse, Rabbit, Pig (94%).

Target Information

Epithelial sodium channels are amiloride-sensitive members of the Degenerin/epithelial sodium channel (Deg/ENaC) superfamily of ion channels. These channels share structural similarity, including two short intracellular amino and carboxyl termini, two membrane-spanning segments, and a large extracellular loop with a conserved cysteine-rich region.
There are three homologous isoforms of the ENaC protein (alpha, beta, and gamma). ENaC in the kidney, lung, and colon plays an essential role in trans-epithelial sodium and fluid balance and mediates aldosterone-dependent sodium reabsorption in the distal nephron, thus regulating blood pressure.
ENaC is thought to be regulated through association with the cystic fibrosis transmembrane conductance regulator (CFTR) chloride ion channel. Gain-of-function mutations in beta- or gamma-ENaC can cause severe arterial hypertension (Liddle’s syndrome), while loss-of-function mutations in alpha- or beta-ENaC cause pseudohypoaldosteronism (PHA-1).


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

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