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Thermo Fisher Scientific GJB2 Monoclonal Antibody (1C6)
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Thermo Fisher Scientific GJB2 Monoclonal Antibody (1C6)

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GJB2 단백질을 인식하는 mouse monoclonal antibody(1C6)로, Western blot과 ELISA에 최적화됨. Human 시료에 반응하며, PBS buffer에 보존된 액상 형태. Affinity chromatography로 정제된 연구용 항체.

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마지막 업데이트 2025. 08. 04. 오후 07:16
Thermo Fisher Scientific H00002706-M01 GJB2 Monoclonal Antibody (1C6) 100 ug pk판매 단위 pk ·
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Thermo Fisher Scientific · Thermo Fisher Scientific GJB2 Monoclonal Antibody (1C6)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–5 µg/mL
ELISA 3 ng/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone 1C6
Immunogen GJB2 (AAH17048, 1 a.a. – 226 a.a.) full-length recombinant protein with GST tag (GST tag MW: 26 kDa)
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Protein sequence:

MDWGTLQTIL GGVNKHSTSI GKIWLTVLFI FRIMILVVAA KEVWGDEQAD FVCNTLQPGC KNVCYDHYFP ISHIRLWALQ LIFVSTPALL VAMHVAYRRH EKKRKFIKGE IKSEFKDIEE IKTQKVRIEG SLWWTYTSSI FFRVIFEAAF MYVFYVMYDG FSMQRLVKCN AWPCPNTVDC FVSRPTEKTV FTVFMIAVSG ICILLNVTEL CYLLIRYCSG KSKKPV

Target Information

Gap junctions are conduits that allow direct cell-to-cell passage of small cytoplasmic molecules, including ions, metabolic intermediates, and second messengers, thereby 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 roles in these channels.
Defects in GJB3 are linked to erythrokeratodermia variabilis (EKV), an autosomal dominant genodermatosis characterized by transient red patches or hyperkeratosis.
Mutations in GJB2 are 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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