Thermo Fisher Scientific Cathepsin K Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA518950 | - | Thermo Fisher Scientific PA518950 Cathepsin K Polyclonal Antibody 100 ug pk | 재고문의 | pk | 701,000원 | - | 771,100원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
0.1-1 µg/mL
Immunocytochemistry (ICC/IF)
10 µg/mL
Product Specifications
Species Reactivity
Human, Rat
Host/Isotype
Goat / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Synthetic peptide sequence (KTHRKQYNNKVDE) corresponding to the internal amino acids of CTSK (aa 31-44). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Cathepsin K,
uniProtId:
P43235-1,
ncbiNodeId:
9606,
antigenRange:
31-44,
antigenLength:
329,
antigenImageFileName:
PA5-18950_Cathepsin_K_P43235-1_Goat.svg,
antigenImageFileNamePDP:
PA5-18950_Cathepsin_K_P43235-1_Goat_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 mg/mL
Purification
Ammonium sulfate precipitation
Storage buffer
TBS, pH 7.3, with 0.5% BSA
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Wet ice
RRID
AB_10981412
Product Specific Information
This antibody is predicted to react with bovine, canine, mouse, porcine and rat based on sequence homology.
This antibody is tested in Peptide ELISA: antibody detection limit dilution 32,000.
Target Information
The protein encoded by this gene is a lysosomal cysteine proteinase involved in bone remodeling and resorption. This protein, which is a member of the peptidase C1 protein family, is predominantly expressed in osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers, where it could contribute to tumor invasiveness. Mutations in this gene are the cause of pycnodysostosis, an autosomal recessive disease characterized by osteosclerosis and short stature. This gene may be subject to RNA editing.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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