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L1CAM Rabbit Polyclonal Antibody (APC)

CAT: 0013-GTR18545978Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18545978Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Anti-L1CAM Antibody. Tested in ELISA, WB applications. This antibody reacts with Human.
Product Name Alternative
CAML1; CD171; HSAS; HSAS1; L1 cell adhesion molecule; L1CAM; MASA; MIC5; N CAM L1; N CAML1; NCAM L1; S10; SPG1
UniProt
P32004
Reactivity
Human
Cross Reactivity
No cross-reactivity with other proteins.
Immunogen
E.coli-derived human L1CAM recombinant protein (Position: I20-L242) .
Target
Neural cell adhesion molecule L1
Clonality
Polyclonal
Conjugation
APC
Field of Research
Cell Biology, Neuroscience, Signal Transduction
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Storage Conditions
At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
Rabbit IgG

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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