Thermo Fisher Scientific Twist1/Twist2 Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA578211 | - | Thermo Fisher Scientific PA578211 Twist1/Twist2 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 733,000원 | - | 806,300원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:10,000
Immunohistochemistry (Paraffin) (IHC (P))
1:100-1:1,000
Product Specifications
Species Reactivity
Fruit fly, Human, Mouse, Rat
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein encompassing a sequence within the center region of human Twist1/2. The exact sequence is proprietary.
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.67 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7, with 20% glycerol
Contains
0.025% 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
RRID
AB_2736761
Product Specific Information
Positive Control: Raji, THP-1, HL-60, TWIST1 transfected 293T lysates, human TWIST1-transfected 293T, Jurkat, OECM1, CL1-5, Toledo, SU-DHL-5, HT, DB, RL95-2, MDA-MB-231
Predicted Reactivity: Japanese Medaka (95%), Xenopus laevis (97%), Chicken (100%), Chimpanzee (100%), Bovine (100%)
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Target Information
Twist1/Twist2 encodes a basic helix-loop-helix (bHLH) transcription factor that plays an important role in embryonic development. The encoded protein forms both homodimers and heterodimers that bind to DNA E box sequences and regulate the transcription of genes involved in cranial suture closure during skull development. This protein may also regulate neural tube closure, limb development and brown fat metabolism. Twist1/Twist2 is hypermethylated and overexpressed in multiple human cancers, and the encoded protein promotes tumor cell invasion and metastasis. Mutations in this gene cause Saethre-Chotzen syndrome in human patients, which is characterized by craniosynostosis, ptosis and hypertelorism.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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