Thermo Fisher Scientific PAX6 (Stem Cell Marker) Monoclonal Antibody (PAX6/7729)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
5080-MSM15-P1 | - | Thermo Fisher Scientific 5080-MSM15-P1 PAX6 (Stem Cell Marker) Monoclonal Antibody (PAX6/7729) 100 ug pk | 재고문의 | pk | 910,000원 | - | 1,001,000원 | |
5080-MSM15-P0 | - | Thermo Fisher Scientific 5080-MSM15-P0 PAX6 (Stem Cell Marker) Monoclonal Antibody (PAX6/7729) 20 ug pk | 재고문의 | pk | 421,000원 | - | 463,100원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
1-2 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG
Class
Monoclonal
Type
Antibody
Clone
PAX6/7729
Immunogen
Recombinant fragment (N-terminus; aa 1-300) of human PAX6 protein if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
PAX6,
uniProtId:
P26367-1,
ncbiNodeId:
9606,
antigenRange:
1-300,
antigenLength:
422,
antigenImageFileName:
5080-MSM15-P0_PAX6_P26367-1_House_mouse.svg,
antigenImageFileNamePDP:
5080-MSM15-P0_PAX6_P26367-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
200 µg/mL
Purification
Protein A/G
Storage buffer
PBS with 0.05% BSA
Contains
0.05% sodium azide
Storage conditions
4° C
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
Positive Control:Human pancreas or cerebellum.
Cellular Location: Nucleus.
Target Information
This gene encodes paired box gene 6, one of many human homologs of the Drosophila melanogaster gene prd. In addition to the hallmark feature of this gene family, a conserved paired box domain, the encoded protein also contains a homeo box domain. Both domains are known to bind DNA, and function as regulators of gene transcription. This gene is expressed in the developing nervous system, and in developing eyes. Mutations in this gene are known to cause ocular disorders such as aniridia and Peter`s anomaly. Alternatively spliced transcript variants encoding either the same or different isoform 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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