Thermo Fisher Scientific alpha Dystroglycan Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA528179 | - | Thermo Fisher Scientific PA528179 alpha Dystroglycan Polyclonal Antibody 100 ul pk | 재고문의 | pk | 648,000원 | - | 712,800원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:3,000
Immunohistochemistry (Paraffin) (IHC (P))
1:100-1:1,000
Immunocytochemistry (ICC/IF)
1:100-1:1,000
Product Specifications
Species Reactivity
Horse, Human, Mouse
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant fragment corresponding to a region within amino acids 471 and 752 of Human alpha Dystroglycan if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
alpha Dystroglycan,
uniProtId:
Q14118-1,
ncbiNodeId:
9606,
antigenRange:
471-752,
antigenLength:
895,
antigenImageFileName:
PA5-28179_alpha_Dystroglycan_Q14118-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-28179_alpha_Dystroglycan_Q14118-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1.28 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_2545655
Product Specific Information
Recommended positive controls: U87-MG, U87-MG membrane fraction extract.
Predicted reactivity: Mouse (92%), Rat (92%), Dog (92%), Cat (95%), Rabbit (94%), Rhesus Monkey (98%), Bovine (93%).
Target Information
Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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