Thermo Fisher Scientific MYO5A Monoclonal Antibody (MUD-19)
상품 옵션 정보 | |||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 재고 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA124948 | - | Thermo Fisher Scientific MA124948 MYO5A Monoclonal Antibody (MUD-19) 50 ul pk | 재고문의 | pk | 645,000원 | - | 709,500원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
2 µg/mL
Immunohistochemistry (IHC)
Assay-dependent
ELISA (ELISA)
Assay-dependent
Immunoprecipitation (IP)
Assay-dependent
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
MUD-19
Immunogen
Synthetic peptide corresponding to residues 291-302 of human MYO6. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MYO5A,
uniProtId:
Q9Y4I1-1,
ncbiNodeId:
9606,
antigenRange:
291-302,
antigenLength:
1855,
antigenImageFileName:
MA1-24948_MYO5A_Q9Y4I1-1_House_mouse.svg,
antigenImageFileNamePDP:
MA1-24948_MYO5A_Q9Y4I1-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1.3 mg/mL
Purification
Protein A
Storage buffer
PBS, pH 7.4, with 1% BSA
Contains
15mM 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_2266842
Product Specific Information
MA1-24948 detects a band ~150 kDa, A suggested positive control for this product is A431 whole cell lysate.
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Target Information
This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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