Thermo Fisher Scientific MYCBP2 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA584393 | - | Thermo Fisher Scientific PA584393 MYCBP2 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 742,000원 | - | 816,200원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunocytochemistry (ICC/IF)
0.25-2 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human MYCBP2. Recombinant protein control fragment (Product #RP-108434). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MYCBP2,
uniProtId:
O75592-1,
ncbiNodeId:
9606,
antigenRange:
3364-3457,
antigenLength:
4678,
antigenImageFileName:
PA5-84393_MYCBP2_O75592-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-84393_MYCBP2_O75592-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.10 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
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_2791545
Product Specific Information
Immunogen sequence: CYHPAKPFQS QLPSVKEGIS EDLPVKMPCL YLQTLARHHH ENFVGYQDDN LFQDEMRYLR STSVPAPYIS VTPDASPNVF EEPESNMKSM PPSL
Target Information
This gene encodes an E3 ubiquitin-protein ligase and member of the PHR (Phr1/MYCBP2, highwire and RPM-1) family of proteins. The encoded protein plays a role in axon guidance and synapse formation in the developing nervous system. In mammalian cells, this protein regulates the cAMP and mTOR signaling pathways, and may additionally regulate autophagy. Reduced expression of this gene has been observed in acute lymphoblastic leukemia patients and a mutation in this gene has been identified in patients with a rare inherited vision defect.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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