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Thermo Fisher Scientific CPS1/Carbamoyl-Phosphate Synthetase Monoclonal Antibody (CPS1, 1022)
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Thermo Fisher Scientific CPS1/Carbamoyl-Phosphate Synthetase Monoclonal Antibody (CPS1, 1022)

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CPS1 단백질을 인식하는 Thermo Fisher Scientific의 단일클론 항체로, 인간 및 개 조직에서 반응합니다. IHC(P) 실험에 적합하며, 고순도의 Protein A/G 정제 항체입니다. PBS 버퍼에 보관되며 연구용으로만 사용 가능합니다.

카탈로그번호
1373-MSM1-P0
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 08:09
Thermo Fisher Scientific 1373-MSM1-P0 CPS1/Carbamoyl-Phosphate Synthetase Monoclonal Antibody (CPS1, 1022) 20 ug pk판매 단위 pk ·
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441,900원VAT 포함 486,090원

Thermo Fisher Scientific · Thermo Fisher Scientific CPS1/Carbamoyl-Phosphate Synthetase Monoclonal Antibody (CPS1, 1022)

Thermo Fisher Scientific CPS1/Carbamoyl-Phosphate Synthetase Monoclonal Antibody (CPS1, 1022)

Applications

  • Immunohistochemistry (Paraffin) (IHC (P))

Tested Dilution: 1–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Dog, Human
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone CPS1, 1022
Immunogen Recombinant human CPS1 protein
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Immunohistochemistry (PFA fixed): incubate antibody for 30 min at room temperature.
Staining of formalin-fixed tissues requires heating tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 45 min at 95°C, followed by cooling at room temperature for 20 minutes.

Target Information

The mitochondrial enzyme encoded by this gene catalyzes synthesis of carbamoyl phosphate from ammonia and bicarbonate. This reaction is the first committed step of the urea cycle, which is essential for removal of excess urea from cells.
The encoded protein may also represent a core mitochondrial nucleoid protein. Three transcript variants encoding different isoforms have been identified for this gene, and the shortest isoform may not be localized to the mitochondrion.
Mutations in this gene have been associated with carbamoyl phosphate synthetase deficiency, susceptibility to persistent pulmonary hypertension, and susceptibility to venoocclusive disease after bone marrow transplantation.


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

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