Thermo Fisher Scientific SNX33 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA559378 | - | Thermo Fisher Scientific PA559378 SNX33 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 776,000원 | - | 853,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
1:500-1:1,000
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human SNX33. Recombinant protein control fragment (Product #RP-98138). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
SNX33,
uniProtId:
Q8WV41-1,
ncbiNodeId:
9606,
antigenRange:
190-242,
antigenLength:
574,
antigenImageFileName:
PA5-59378_SNX33_Q8WV41-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-59378_SNX33_Q8WV41-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 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_2647728
Product Specific Information
Immunogen sequence: VRSGVEAFIL GDVPMMAKIA ETYSIEMGPR GPQWKANPHP FACSVEDPTK QTK
Highest antigen sequence identity to the following orthologs: Mouse - 98%, Rat - 98%.
Target Information
SNX33 (sorting nexin-33), also known as SH3PX3, SH3PXD3C or SNX30, is a 574 amino acid protein that interacts with ADAM15 and FAS-L. Belonging to the sorting nexin family, SNX33 contains one BAR domain, one PX (phox homology) domain and one SH3 domain. The gene that encodes SNX33 consists of over 14,000 bases and maps to human chromosome 15q24.2. Housing approximately 106 million base pairs and encoding more than 700 genes, chromosome 15 makes up about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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