Thermo Fisher Scientific KIAA0196 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA567132 | - | Thermo Fisher Scientific PA567132 KIAA0196 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 794,000원 | - | 873,400원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunocytochemistry (ICC/IF)
0.25-2 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant Human KIAA0196. Recombinant protein control fragment (Product #RP-107779). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
KIAA0196,
uniProtId:
Q12768-1,
ncbiNodeId:
9606,
antigenRange:
723-815,
antigenLength:
1159,
antigenImageFileName:
PA5-67132_KIAA0196_Q12768-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-67132_KIAA0196_Q12768-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.1 mg/mL
Purification
Antigen affinity chromatography
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_2663199
Product Specific Information
Immunogen sequence: HRGLIFNPRAK PSELMPKLKE LGATMDGFHR SFEYIQDYVN IYGLKIWQEE VSRIINYNVE QECNNFLRTK IQDWQSMYQS THIPIPKFTP VD
Highest antigen sequence identity to the following orthologs - mouse 98%, rat 98%.
Target Information
This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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