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Thermo Fisher Scientific BRAF (V600E Mutant Specific) (Prognostic Marker) Monoclonal Antibody (V600E/1322)
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Thermo Fisher Scientific BRAF (V600E Mutant Specific) (Prognostic Marker) Monoclonal Antibody (V600E/1322)

상품 한눈에 보기

BRAF(V600E) 변이 특이적 단일클론 항체로, 인간 시료에 반응하며 예후 마커 연구용으로 적합. ELISA 등 다양한 분석에 사용 가능. 단백질 A로 정제된 액상 항체로, 4°C에서 보관. 연구용으로만 사용.

카탈로그번호
673-MSM2-Px (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 03. 오후 11:00
Thermo Fisher Scientific 673-MSM2-P1 BRAF (V600E Mutant Specific) (Prognostic Marker) Monoclonal Antibody (V600E/1322) 100 ug pk판매 단위 pk ·
재고 확인 필요
900,300원VAT 포함 990,330원
Thermo Fisher Scientific 673-MSM2-P0 BRAF (V600E Mutant Specific) (Prognostic Marker) Monoclonal Antibody (V600E/1322) 20 ug pk판매 단위 pk ·
재고 확인 필요
449,700원VAT 포함 494,670원

Thermo Fisher Scientific · Thermo Fisher Scientific BRAF (V600E Mutant Specific) (Prognostic Marker) Monoclonal Antibody (V600E/1322)

Applications

  • ELISA (ELISA): Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG, kappa
Class Monoclonal
Type Antibody
Clone V600E/1322
Immunogen An eleven amino acid residue long synthetic peptide (aa596-606), corresponding to Cys-GLAT(E)KSRWSG from human BRAF protein. It was conjugated to KLH at the N-terminus.
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C, do not freeze
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

The B-RAF/BRAF gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein regulates the MAP kinase/ERK signaling pathway, influencing cell division, differentiation, and secretion.
Mutations in this gene, particularly the V600E mutation, are among the most common cancer-causing mutations in melanoma and have also been identified in other cancers such as non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia, and lung adenocarcinoma.
Additionally, mutations are associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome.


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

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