Thermo Fisher Scientific CLN5 Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA559730 | - | Thermo Fisher Scientific PA559730 CLN5 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 776,000원 | - | 853,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
0.04-0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
1:500-1:1,000
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human CLN5. Recombinant protein control fragment (Product #RP-97938). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
CLN5,
uniProtId:
O75503-1,
ncbiNodeId:
9606,
antigenRange:
125-220,
antigenLength:
358,
antigenImageFileName:
PA5-59730_CLN5_O75503-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-59730_CLN5_O75503-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.4 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_2639894
Product Specific Information
Immunogen sequence: TLTGKNYTME WYELFQLGNC TFPHLRPEMD APFWCNQGAA CFFEGIDDVH WKENGTLVQV ATISGNMFNQ MAKWVKQDNE TGIYYETWNV KASPEK
Highest antigen sequence identity to the following orthologs: Mouse - 83%, Rat - 85%.
Target Information
This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008].
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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