Thermo Fisher Scientific Nkx2.5 Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA549431 | - | Thermo Fisher Scientific PA549431 Nkx2.5 Polyclonal Antibody 200 ul pk | 재고문의 | pk | 632,000원 | - | 695,200원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000
View 1 publication 1 publication
Immunohistochemistry (IHC)
-
View 3 publications 3 publications
Immunohistochemistry (Paraffin) (IHC (P))
1:500
Immunocytochemistry (ICC/IF)
1:25
View 3 publications 3 publications
Flow Cytometry (Flow)
1:25
View 2 publications 2 publications
ChIP assay (ChIP)
-
View 2 publications 2 publications
Product Specifications
Species Reactivity
Human, Mouse
Published species
Human, Mouse, Zebrafish
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
KLH conjugated synthetic peptide between 98-133 amino acids from the Central region of mouse Nkx2-5. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Nkx2.5,
uniProtId:
P42582-1,
ncbiNodeId:
10090,
antigenRange:
98-133,
antigenLength:
318,
antigenImageFileName:
PA5-49431_Nkx2.5_P42582-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-49431_Nkx2.5_P42582-1_Rabbit_PDP.jpeg,
sortOrder:
2}\]
; $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
Protein A, Antigen affinity chromatography
Storage buffer
PBS, pH 7.4
Contains
0.09% 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_2634885
Target Information
This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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