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Thermo Fisher Scientific TWIST1 Monoclonal Antibody (2F8E7)
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Thermo Fisher Scientific TWIST1 Monoclonal Antibody (2F8E7)

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TWIST1 단백질을 인식하는 Mouse Monoclonal Antibody(2F8E7)로, Human 시료에 반응합니다. Western blot, ELISA, ICC/IF 등 다양한 응용에 적합하며, 고순도 Protein G 정제 및 안정적인 액상 형태로 제공됩니다.

카탈로그번호
MA517195
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 08:11
Thermo Fisher Scientific MA517195 TWIST1 Monoclonal Antibody (2F8E7) 100 ug pk판매 단위 pk ·
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603,200원VAT 포함 663,520원

Thermo Fisher Scientific · Thermo Fisher Scientific TWIST1 Monoclonal Antibody (2F8E7)

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:2,000 View 1 publication
Immunohistochemistry (Frozen) (IHC (F)) - View 1 publication
Immunocytochemistry (ICC/IF) 1:200 View publication
ELISA 1:10,000 View publication

Product Specifications

Specification Description
Species Reactivity Human
Published Species Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone 2F8E7
Immunogen Purified recombinant fragment of human TWIST1 (amino acids 9–74) expressed in E. coli
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term; for long term, store at -20°C and avoid freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2538666

Product Specific Information

MA5-17195 targets TWIST1 in indirect ELISA and WB applications, showing reactivity with Human samples.
The immunogen is a purified recombinant fragment of human TWIST1 (amino acids 9–74) expressed in E. coli.
MA5-17195 detects TWIST1, which has a predicted molecular weight of approximately 21 kDa.


Target Information

TWIST1 acts as a transcriptional regulator. It inhibits myogenesis by sequestering E proteins, suppresses trans-activation by MEF2, and blocks DNA-binding by MYOD1 through physical interaction.
TWIST1 also represses proinflammatory cytokines such as TNFA and IL1B, and regulates cranial suture patterning and fusion. Mutations in TWIST1 are implicated in Saethre-Chotzen syndrome, characterized by coronal synostosis, brachycephaly, facial asymmetry, hypertelorism, broad halluces, and clinodactyly.


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

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