Thermo Fisher Scientific Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Recombinant Rabbit Monoclonal Antibody (DMD/8773R)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
1756-RBM10-P0 | - | Thermo Fisher Scientific 1756-RBM10-P0 Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Recombinant Rabbit Monoclonal An pk | 재고문의 | pk | 447,000원 | - | 491,700원 | |
1756-RBM10-P1 | - | Thermo Fisher Scientific 1756-RBM10-P1 Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Recombinant Rabbit Monoclonal An pk | 재고문의 | pk | 0원 | - | 0원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1-2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA))
1-2 µg/mL
Immunocytochemistry (ICC/IF)
2-4 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG, kappa
Expression System
CHO cells
Class
Recombinant Monoclonal
Type
Antibody
Clone
DMD/8773R
Immunogen
Recombinant fragment (around aa1700-2300) of human DMD.. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Dystrophin,
uniProtId:
P11532-1,
ncbiNodeId:
9606,
antigenRange:
1700-2300,
antigenLength:
3685,
antigenImageFileName:
1756-RBM10-P0_Dystrophin_P11532-1_Rabbit.svg,
antigenImageFileNamePDP:
1756-RBM10-P0_Dystrophin_P11532-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
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, do not freeze
Shipping conditions
Ambient (domestic); Wet ice (international)
Target Information
Dystrophin is the 427kDa protein product of the DMB/BMD gene located on the X chromosome at position Xp21. Western blotting and immunohistochemistry are the two established methods for the detection of abnormalities of dystrophin expression in muscle biopsies. Dystrophin abnormalities are thought to occur in 100% of patients with DMD/BMD, although genetic abnormalities may only be detected in up to 65% of cases.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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