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Thermo Fisher Scientific Connexin 31 Polyclonal Antibody
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Thermo Fisher Scientific Connexin 31 Polyclonal Antibody

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Connexin 31 단백질을 인식하는 토끼 폴리클로날 항체로, Western blot에 적합합니다. Mouse에 반응하며, 합성 펩타이드 면역원으로 제작되었습니다. 액상 형태, 0.5 mg/mL 농도, -20°C 보관. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 07. 30. 오전 08:41
Thermo Fisher Scientific PA5113757 Connexin 31 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
680,400원VAT 포함 748,440원

Thermo Fisher Scientific · Thermo Fisher Scientific Connexin 31 Polyclonal Antibody

Thermo Fisher Scientific Connexin 31 Polyclonal Antibody

Applications

  • Western Blot (WB): Tested dilution 0.125 µg/mL

Product Specifications

항목 내용
Species Reactivity Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide directed towards the N-terminal region of Mouse Gjb3 (aa 1–50)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 2% sucrose
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2884272

Product Specific Information

  • Immunogen sequence: MDWKKLQDLL SGVNQYSTAF GRIWLSVVFV FRVLVYVVAA ERVWGDEQKD
  • Storage recommendations:
    • Short term: Store at 2–8°C up to 1 week
    • Long term: Store at -20°C in small aliquots to prevent freeze-thaw cycles
  • Predicted homology:
    Cow 79%, Dog 83%, Horse 83%, Human 83%, Mouse 100%, Pig 83%, Rabbit 79%, Rat 100%, Zebrafish 92%

Target Information

Gap junctions are conduits that allow the direct cell-to-cell passage of small cytoplasmic molecules, including ions, metabolic intermediates, and second messengers, and thereby mediate intercellular metabolic and electrical communication. Gap junction channels consist of connexin protein subunits, which are 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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