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Thermo Fisher Scientific Npr2 Recombinant Rabbit Monoclonal Antibody (ARC2421)
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Thermo Fisher의 Npr2 Recombinant Rabbit Monoclonal Antibody (ARC2421)는 Mouse 시료에 반응하며 Western Blot과 ELISA에 적합합니다. HEK293 세포에서 발현된 재조합 단클론 항체로, 고순도 Affinity chromatography로 정제되었습니다. 연구용으로만 사용됩니다.
- 판매단위
- pk
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Thermo Fisher Scientific MA537887 Npr2 Recombinant Rabbit Monoclonal Antibody (ARC2421) 100 ul pk판매 단위 pk ·
재고 확인 필요
699,900원VAT 포함 769,890원
Thermo Fisher Scientific · Thermo Fisher Scientific Npr2 Recombinant Rabbit Monoclonal Antibody (ARC2421)
Applications
Western Blot (WB)
- Tested Dilution: 1:500–1:1,000
ELISA
- Tested Dilution: 1 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Mouse |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | ARC2421 |
| Immunogen | A synthetic peptide corresponding to amino acids 800–900 of human ANPRB/NRP2 (P20594) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.3, with 50% glycerol, 0.05% BSA |
| Contains | 0.02% sodium azide |
| Storage Conditions | −20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2897807 |
Product Specific Information
- Positive Samples: Mouse lung, Mouse spleen
- Immunogen sequence:
NLLLRMEQYA NNLEKLVEER TQAYLEEKRK AEALLYQILP HSVAEQLKRG ETVQAEAFDS VTIYFSDIVG FTALSAESTP MQVVTLLNDL YTCFDAIIDN F
Target Information
This gene encodes natriuretic peptide receptor B, one of two integral membrane receptors for natriuretic peptides.
Both NPR1 and NPR2 contain five functional domains:
- Extracellular ligand-binding domain
- Single membrane-spanning region
- Intracellular protein kinase homology domain
- Helical hinge region involved in oligomerization
- Carboxyl-terminal guanylyl cyclase catalytic domain
The protein is the primary receptor for C-type natriuretic peptide, which upon ligand binding exhibits greatly increased guanylyl cyclase activity.
Mutations in this gene are the cause of acromesomelic dysplasia Maroteaux type.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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