Thermo Fisher Scientific Dystrophin Monoclonal Antibody (1808)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA513526 | - | Thermo Fisher Scientific MA513526 Dystrophin Monoclonal Antibody (1808) 500 ul pk | 재고문의 | pk | 0원 | - | 0원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (IHC)
-
View 1 publication 1 publication
Immunohistochemistry (Paraffin) (IHC (P))
2-4 µg/mL
Immunocytochemistry (ICC/IF)
-
View 1 publication 1 publication
Product Specifications
Published species
Human
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
1808
Immunogen
Acetylcholine receptor (AChR)-enriched membranes and peripheral membrane proteins from Torpedo nobiliana electric organ if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Dystrophin,
uniProtId:
P11532-1,
ncbiNodeId:
9606,
antigenRange:
1-3685,
antigenLength:
3685,
antigenImageFileName:
MA5-13526_Dystrophin_P11532-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-13526_Dystrophin_P11532-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.8 mg/mL
Storage conditions
4° C
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_11000900
Product Specific Information
MA5-13526 targets Dystrophin in IF, IHC (P) applications and shows reactivity with Human samples.
The MA5-13526 immunogen is acetylcholine receptor (AChR)-enriched membranes and peripheral membrane proteins from Torpedo nobiliana electric organ.
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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