
Thermo Fisher Scientific TWIST1 Monoclonal Antibody (2F8E7)
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:2,000
View 1 publication 1 publication
Immunohistochemistry (Frozen) (IHC (F))
-
View 1 publication 1 publication
Immunocytochemistry (ICC/IF)
1:200
ELISA (ELISA)
1:10,000
Product Specifications
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. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
TWIST1,
uniProtId:
Q15672-1,
ncbiNodeId:
9606,
antigenRange:
9-74,
antigenLength:
202,
antigenImageFileName:
MA5-17195_TWIST1_Q15672-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-17195_TWIST1_Q15672-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated 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 storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2538666
Product Specific Information
MA5-17195 targets TWIST1 in indirect ELISA, WB applications and shows reactivity with Human samples.
The MA5-17195 immunogen is 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 21kDa.
Target Information
TWIST1 acts as a transcriptional regulator. It inhibits myogensis by sequestering E proteins, inhibiting trans-activation by MEF2, and inhibiting DNA-binding by MYOD1 through physical interaction. TWIST1 also represses proinflammatory cytokines such as TNFA and IL1B. TWIST also regulates cranial suture patterning and fusion and gene expression differentially depending on dimer composition. Mutations in the gene are implicated in Saethre-Chotzen syndrome, a disease characterized by coronal synostosis, brachycephaly, low front hairline, 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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