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Thermo Fisher Scientific L1CAM Monoclonal Antibody (UMAB47), UltraMAB
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Thermo Fisher Scientific L1CAM Monoclonal Antibody (UMAB47), UltraMAB

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L1CAM 단백질을 인식하는 UMAB47 단클론 항체로, Western blot, IHC, ICC, ChIP 등 다양한 응용에 사용 가능. 인간 시료에 반응하며, PBS와 trehalose 완충액에 동결건조 형태로 제공. 신경계 발달 및 세포 부착 관련 연구에 적합.

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UM500043CF
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 03:14
Thermo Fisher Scientific UM500043CF L1CAM Monoclonal Antibody (UMAB47), UltraMAB 100 ug pk판매 단위 pk ·
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883,700원VAT 포함 972,070원

Thermo Fisher Scientific · Thermo Fisher Scientific L1CAM Monoclonal Antibody (UMAB47), UltraMAB

Applications and Tested Dilutions

Application Tested Dilution Notes
Western Blot (WB) Assay-dependent
Immunohistochemistry (Paraffin) (IHC-P) 1:100
Immunocytochemistry (ICC/IF) 1:100
ChIP assay (ChIP) Assay-dependent
Peptide Array (Array) Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone UMAB47
Immunogen Full length human recombinant protein of human L1CAM produced in HEK293T cells (target family: CD171 (L1CAM), UniProt ID: P32004-1, antigen range: 1–1257)
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, it is recommended to perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).


Target Information

L1CAM (CD171) is an axonal glycoprotein of the immunoglobulin superfamily. Its ectodomain contains several immunoglobulin-like and fibronectin type III domains, linked through a single transmembrane region to a conserved cytoplasmic domain.
L1CAM plays a crucial role in nervous system development, including 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, and hydrocephalus).
Alternative splicing of a neuron-specific exon is functionally relevant.


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

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