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Thermo Fisher Scientific Connexin 26 Polyclonal Antibody
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Thermo Fisher Scientific Connexin 26 Polyclonal Antibody

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Connexin 26 단백질을 인식하는 Goat Polyclonal Antibody로, WB, IHC, Flow Cytometry에 적합합니다. 인간, 생쥐, 랫트 반응성을 보이며, 0.5 mg/mL 농도의 액상 형태로 제공됩니다. 연구용으로만 사용 가능합니다.

카탈로그번호
PA518618
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 10:25
Thermo Fisher Scientific PA518618 Connexin 26 Polyclonal Antibody 100 ug pk판매 단위 pk ·
재고 확인 필요
619,800원VAT 포함 681,780원

Thermo Fisher Scientific · Thermo Fisher Scientific Connexin 26 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 0.01–1 µg/mL -
Immunohistochemistry (IHC) View 1 publication
Flow Cytometry (Flow) 10 µg/mL -

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Goat / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide sequence (YLLIRYCSGKSKKP) corresponding to the C-terminus amino acids of GJB2 (aa 212–225)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Ammonium sulfate precipitation
Storage Buffer TBS, pH 7.3, with 0.5% BSA
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_10982506

Product Specific Information

  • Predicted to react with human and rat based on sequence homology.
  • Tested in Peptide ELISA: antibody detection limit dilution 1:128,000.

Target Information

Gap junctions are conduits that allow direct cell-to-cell passage of small cytoplasmic molecules, including ions, metabolic intermediates, and second messengers, mediating intercellular metabolic and electrical communication.
Gap junction channels consist of connexin protein subunits encoded by a multigene family.
GJBs (gap-junction proteins or connexins) play crucial functional roles associated with these channels.
Defects in GJB3 have been linked to erythrokeratodermia variabilis (EKV), an autosomal dominant genodermatosis characterized by transient figurate red patches or hyperkeratosis.
Mutations in GJB2 have also been associated with genetically derived hearing impairments, including autosomal recessive nonsyndromic deafness.


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

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