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Thermo Fisher Scientific EDAR Chimeric Recombinant Rabbit Monoclonal Antibody (EDAR12)
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Thermo Fisher Scientific EDAR Chimeric Recombinant Rabbit Monoclonal Antibody (EDAR12)

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EDAR 단백질을 인식하는 재조합 토끼 단클론 항체로, 다양한 종(인간, 마우스, 개, 닭, 랫드)에 반응합니다. WB, ELISA, 기능 분석, SPR 등 다양한 응용에 사용 가능하며, 1 mg/mL 농도의 액상 형태로 제공됩니다. 단백질 A로 정제되어 높은 특이성과 재현성을 제공합니다.

판매단위
pk
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마지막 업데이트 2025. 07. 30. 오전 04:02
Thermo Fisher Scientific MA551727 EDAR Chimeric Recombinant Rabbit Monoclonal Antibody (EDAR12) 200 ug pk판매 단위 pk ·
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873,900원VAT 포함 961,290원

Thermo Fisher Scientific · Thermo Fisher Scientific EDAR Chimeric Recombinant Rabbit Monoclonal Antibody (EDAR12)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) Assay-dependent
ELISA Assay-dependent
Functional Assay Assay-dependent
Surface Plasmon Resonance (SPR) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Dog, Chicken, Human, Mouse, Rat
Host / Isotype Rabbit / IgG, kappa
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone EDAR12
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer PBS
Contains 0.02% ProClin 300
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice

Immunogen

EDAR12 was prepared by immunizing female OVE1B mice (with the Edar gene deleted) subcutaneously with mouse EDAR-Fc. Positive hybridoma clones were screened for binding mEDAR by ELISA.

Product Specific Information

EDAR12 recognises and binds to CRD1 of the extracellular domain of mouse EDAR.
EDAR3 cross-reacts with EDAR derived from human, dog, rat, and chicken when EDAR is fused to the glycosylphosphatidylinositol anchor of TRAILR3.
EDAR is the receptor for the TNF family ligand EDA1, a type II transmembrane protein possessing a collagen-like domain and a C-terminal TNF-homology domain.
EDAR plays a crucial role in the proper development of skin appendages including hair, teeth, and eccrine sweat glands.
Loss-of-function mutations in the Eda gene are known to cause XLHED (X-linked hypohidrotic ectodermal dysplasia), leading to abnormal development.

Target Information

This gene encodes a member of the tumor necrosis factor receptor family. The encoded transmembrane protein is a receptor for the soluble ligand ectodysplasin A and can activate the nuclear factor-kappaB, JNK, and caspase-independent cell death pathways.
It is essential for the development of hair, teeth, and other ectodermal derivatives.
Mutations in this gene result in autosomal dominant and recessive forms of hypohidrotic ectodermal dysplasia.


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

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