Thermo Fisher Scientific ZIC4 Monoclonal Antibody (1A9)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
H00084107-M05 | - | Thermo Fisher Scientific H00084107-M05 ZIC4 Monoclonal Antibody (1A9) 100 ug pk | 재고문의 | pk | 520,000원 | - | 572,000원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1-5 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
3 µg/mL
Immunocytochemistry (ICC/IF)
10 µg/mL
ELISA (ELISA)
0.03 ng/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2a, kappa
Class
Monoclonal
Type
Antibody
Clone
1A9
Immunogen
ZIC4 (NP_115529, 249 a.a. approximately 319 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
ZIC4,
uniProtId:
Q8N9L1-1,
ncbiNodeId:
9606,
antigenRange:
249-319,
antigenLength:
334,
antigenImageFileName:
H00084107-M05_ZIC4_Q8N9L1-1_House_mouse.svg,
antigenImageFileNamePDP:
H00084107-M05_ZIC4_Q8N9L1-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
See Label
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.4
Contains
no preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
Sequence of this protein is as follows: SDRKKHSHVH TSDKPYTCKV RGCDKCYTHP SSLRKHMKVH GRSPPPSSGY DSATPSALVS PSSDCGHKSQ V
Target Information
This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. Members of this family are important during development, and have been associated with X-linked visceral heterotaxy and holoprosencephaly type 5. This gene is closely linked to the gene encoding zinc finger protein of the cerebellum 1, a related family member on chromosome 3. Heterozygous deletion of these linked genes is involved in Dandy-Walker malformation, which is a congenital cerebellar malformation. Multiple transcript variants have been identified for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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