Thermo Fisher Scientific SIX1 Monoclonal Antibody (CL0185)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA524588 | - | Thermo Fisher Scientific MA524588 SIX1 Monoclonal Antibody (CL0185) 100 ul pk | 재고문의 | pk | 802,000원 | - | 882,200원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
1:200-1:500
Immunocytochemistry (ICC/IF)
2-10 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
CL0185
Immunogen
Recombinant protein corresponding to Human SIX1 if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
SIX1,
uniProtId:
Q15475-1,
ncbiNodeId:
9606,
antigenRange:
130-270,
antigenLength:
284,
antigenImageFileName:
MA5-24588_SIX1_Q15475-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-24588_SIX1_Q15475-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Protein A
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_2637203
Product Specific Information
Immunogen sequence: CFKEKSRGVL REWYAHNPYP SPREKRELAE ATGLTTTQVS NWFKNRRQRD RAAEAKEREN TENNNSSSNK QNQLSPLEGG KPLMSSSEEE FSPPQSPDQN SVLLLQGNMG HARSSNYSLP GLTASQPSHG LQTHQHQLQD S
Highest antigen sequence identity to the following orthologs: Mouse - 99%, Rat - 99%.
Target Information
The protein encoded by this gene is a homeobox protein that is similar to the Drosophila sine oculis
gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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