Thermo Fisher Scientific CD171 Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA582219 | - | Thermo Fisher Scientific PA582219 CD171 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 764,000원 | - | 840,400원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
1:200-1:500
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human L1CAM. Recombinant protein control fragment (Product #RP-92121). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
CD171 (L1CAM),
uniProtId:
P32004-1,
ncbiNodeId:
9606,
antigenRange:
974-1120,
antigenLength:
1257,
antigenImageFileName:
PA5-82219_CD171_L1CAM_P32004-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-82219_CD171_L1CAM_P32004-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.2 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_2789380
Product Specific Information
Immunogen sequence: ELRTHNLTDL SPHLRYRFQL QATTKEGPGE AIVREGGTMA LSGISDFGNI SATAGENYSV VSWVPKEGQC NFRFHILFKA LGEEKGGASL SPQYVSYNQS SYTQWDLQPD TDYEIHLFKE RMFRHQMAVK TNGTGRVRLP PAGFATE
Target Information
L1CAM/CD171 is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause three X-linked neurological syndromes known by the acronym CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of a neuron-specific exon is thought to be functionally relevant.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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