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Thermo Fisher Scientific Cytokeratin 16 (KRT16) (Suprabasal Keratinocyte Marker) Recombinant Rabbit Monoclonal Antibody (KRT16/2043R)
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Thermo Fisher Scientific Cytokeratin 16 (KRT16) (Suprabasal Keratinocyte Marker) Recombinant Rabbit Monoclonal Antibody (KRT16/2043R)

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Recombinant rabbit monoclonal antibody targeting Cytokeratin 16 (KRT16), a suprabasal keratinocyte marker. Suitable for IHC applications. High purity via Protein A/G purification. Supplied as unconjugated liquid form, 1 mg/mL in PBS buffer. For researc...

카탈로그번호
3868-RBM3-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 06:24
Thermo Fisher Scientific 3868-RBM3-P1ABX Cytokeratin 16 (KRT16) (Suprabasal Keratinocyte Marker) Recombinant Rabbit Monoclonal Antibody (KRT1 pk판매 단위 pk ·
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1,063,800원VAT 포함 1,170,180원

Thermo Fisher Scientific · Thermo Fisher Scientific Cytokeratin 16 (KRT16) (Suprabasal Keratinocyte Marker) Recombinant Rabbit Monoclonal Antibody (KRT16/2043R)

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Assay-dependent

Immunohistochemistry (PFA fixed) (IHC (PFA))

  • 1–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone KRT16/2043R
Immunogen Recombinant fragment from the C-terminal of human Cytokeratin 16
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

KRT16 is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins arranged in pairs of heterotypic keratin chains and are clustered in a region of chromosome 17q12–q21.
This keratin has been coexpressed with keratin 14 in epithelial tissues such as esophagus, tongue, and hair follicles. Mutations in this gene are associated with type 1 pachyonychia congenita, non-epidermolytic palmoplantar keratoderma, and unilateral palmoplantar verrucous nevus.


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

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