Thermo Fisher Scientific WRB Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA19557 | - | Thermo Fisher Scientific PA19557 WRB Polyclonal Antibody 500 ug pk | 재고문의 | pk | 513,000원 | - | 564,300원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:5,000
Product Specifications
Species Reactivity
Human
Host/Isotype
Chicken / IgY
Class
Polyclonal
Type
Antibody
Immunogen
Purified recombinant WRB corresponding to the chromosome 21 gene (Human). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
WRB,
uniProtId:
O00258-1,
ncbiNodeId:
9606,
antigenRange:
1-174,
antigenLength:
174,
antigenImageFileName:
PA1-9557_WRB_O00258-1_Chicken.svg,
antigenImageFileNamePDP:
PA1-9557_WRB_O00258-1_Chicken_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
IgY fraction
Storage buffer
PBS
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
Ambient (domestic); Wet ice (international)
RRID
AB_2215936
Product Specific Information
PA1-9557 detects WRB in human samples.
PA1-9557 has been successfully used in Western blot procedures. By Western blot, PA1-9557 detects a 16 kDa protein representing WRB.
PA1-9557 immunogen is a purified recombinant WRB corresponding to the chromosome 21 gene (Human).
Store at 4C for up to 1 week. Store at -20C long term.
Target Information
This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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