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Thermo Fisher Scientific CD171 (L1CAM) Chimeric Recombinant Rabbit Monoclonal Antibody (L1-14.10)
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Thermo Fisher Scientific CD171 (L1CAM) Chimeric Recombinant Rabbit Monoclonal Antibody (L1-14.10)

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인간 L1CAM/CD171 단백질의 ectodomain을 인식하는 재조합 토끼 단클론 항체로, WB, IHC, ICC/IF, Flow, IP 등 다양한 어세이에 사용 가능. 높은 특이성과 순도, Protein A 정제, 장기 보관 시 -20°C 권장.

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pk
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마지막 업데이트 2025. 07. 25. 오전 10:17
Thermo Fisher Scientific MA548244 CD171 (L1CAM) Chimeric Recombinant Rabbit Monoclonal Antibody (L1-14.10) 200 ug pk판매 단위 pk
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696,000원VAT 포함 765,600원

Thermo Fisher Scientific · Thermo Fisher Scientific CD171 (L1CAM) Chimeric Recombinant Rabbit Monoclonal Antibody (L1-14.10)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) Assay-dependent
Immunohistochemistry (IHC) Assay-dependent
Immunocytochemistry (ICC/IF) Assay-dependent
Flow Cytometry (Flow) Assay-dependent
Immunoprecipitation (IP) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG, kappa
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone L1-14.10
Immunogen Recombinant L1-Fc fusion protein (ectodomain of human L1)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer PBS
Contains 0.02% ProClin 300
Storage Conditions Store at 4°C short term; for long term, store at -20°C (avoid freeze/thaw cycles)
Shipping Conditions Wet ice
RRID AB_3074686

Product Specific Information

This antibody specifically recognizes the ectodomain (amino acids M1–E1123) of human L1, targeting an epitope in the third Ig domain.
L1 is over-expressed in various tumors including neuroblastomas, renal carcinomas, ovarian and endometrial carcinomas, and melanomas.
No cross-reactivity with human CHL1.

Target Information

L1CAM/CD171 is an axonal glycoprotein belonging to the immunoglobulin supergene family.
Its ectodomain consists of several immunoglobulin-like domains and fibronectin-like type III repeats, linked via a transmembrane sequence to a conserved cytoplasmic domain.
This cell adhesion molecule is critical for nervous system development, neuronal migration, and differentiation.
Mutations in the L1CAM gene cause X-linked neurological syndromes collectively known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia, hydrocephalus).
Alternative splicing of a neuron-specific exon is functionally relevant.


For Research Use Only.
Not for use in diagnostic procedures or resale without express authorization.

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