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L1CAM Antibody

CAT: 0667-KC-1806-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0667-KC-1806-01Size:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Product Name Alternative
Neural cell adhesion molecule L1, N-CAM-L1, NCAM-L1, CD antigen CD171
Gene Name
L1CAM
Gene ID
3897
UniProt
P32004
Antigen Species
Human
Reactivity
Human
Cross Reactivity
Not tested
Immunogen
Human L1CAM peptide
Target Antigen
CD171
Partner Proteins
Neural cell adhesion molecule L1; N-CAM-L1; NCAM-L1; CD antigen CD171
Clone
KAA387_7D12
Conjugation
Unconjugated
Applications
Top_IHC&ELISA
Validation
Top_IHC&ELISA
Detection Method
Succeed
Purity
≥85%
Storage Temperature
Avoid repeated freeze-thaw cycles. Upon receipt, * 1 month when stored at 2 to 8 °C * 12 months when aliquoted and stored at -20 °C or lower
Recombinant Antibody
Not recombinant
IHC Dilution
1:200
Sandwich ELISA Dilution
1:200
Formulation
Phosphate-buffered saline (PBS) with 50% glycerol, 0.5% BSA and 0.09% sodium azide
Antibody Type
Monoclonal
Gene Name Synonym
CAML1; MIC5
Target Alternative Name
L1CAM
Panel Description
CD Antigen, Neuroscience Biomarkers
Host or Source
Mouse
Protein Name
L1 cell adhesion molecule
IHC description
Succeed
IP description
Fail (HeLa)
Shipping Temperature
Shipped at ambient temperature or with ice packs.
Isotype
IgG1

UniProtKB · P32004

Neural cell adhesion molecule L1

L1CAM_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P32004
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
L1CAM
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
N-CAM-L1, NCAM-L1
EC number
—
Processing
Precursor
Secondary accessions
A0AV65, A4ZYW4, B2RMU7, G3XAF4, Q8TA87
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Biological process

Cell adhesionDifferentiationNeurogenesis

Cellular component

Cell membraneCell projectionMembrane

Molecular function

Developmental protein

Disease

Disease variantHereditary spastic paraplegiaHirschsprung diseaseIntellectual disabilityNeurodegeneration

PTM

Disulfide bondGlycoproteinPhosphoprotein

Domain

Immunoglobulin domainRepeatSignalTransmembraneTransmembrane helix

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