Thermo Fisher Scientific PCDH15 Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA547865 | - | Thermo Fisher Scientific PA547865 PCDH15 Polyclonal Antibody 100 ug pk | 재고문의 | pk | 707,000원 | - | 777,700원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
5-15 µg/mL
Immunocytochemistry (ICC/IF)
5-15 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Sheep / IgG
Class
Polyclonal
Type
Antibody
Immunogen
CHO-derived recombinant human Protocadherin-15 Gln27-Ala1376 if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
PCDH15,
uniProtId:
Q96QU1-1,
ncbiNodeId:
9606,
antigenRange:
27-1376,
antigenLength:
1955,
antigenImageFileName:
PA5-47865_PCDH15_Q96QU1-1_Sheep.svg,
antigenImageFileNamePDP:
PA5-47865_PCDH15_Q96QU1-1_Sheep_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Lyophilized
Concentration
0.2 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS with 5% trehalose
Contains
No Preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2605929
Product Specific Information
In direct ELISAs, less than 1% cross-reactivity with recombinant human (rh) Protocadherin-1, rhProtocadherin-8, and rhProtocadherin-10 is observed.
Reconstitute in sterile PBS to a final concentration of 0.2 mg/mL.
Target Information
PCDH15 is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. PCDH15 consists of a signal peptide, 11 extracellular calcium-binding domains, a transmembrane domain and a unique cytoplasmic domain. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene have been associated with hearing loss, which is consistent with its location at the Usher syndrome type 1F (USH1F) critical region on chromosome 10.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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