Anti-L1CAM抗体[UJ127.11] (ab20148)


  • 产品名称Anti-L1CAM抗体[UJ127.11]
    参阅全部 L1CAM 一抗
  • 描述
    小鼠单克隆抗体[UJ127.11] to L1CAM
  • 特异性UJ127.11 may be useful in the diagnosis of embryonic tumours (e.g. neuroblastoma).
  • 经测试应用适用于: WB, IP, IHC-Pmore details
  • 种属反应性
    与反应: Human
  • 免疫原

    Tissue, cells or virus corresponding to Human L1CAM. Homogenous suspension of 16 week human foetal brain.
    Database link: P32004

  • 常规说明L1CAM can be detected between 200-220 kD. In brain samples it is typically seen at ~ 200 kD. When the protein is overexpressed in vitro it is often detected as a doublet with bands at 200 and 220 kD. The unglycosylated, unprocessed L1CAM is ~ 140-150 kDa. The protein has 21 putative N-glycosylation sites on the extracellular portion of the protein which, when they are all glycosylated, results in a detected MW of 200-220 kD depending upon how many residues are actually glycosylated. L1CAM can be cleaved by the metalloprotease ADAM10 resulting in fragments of 180 kD and 40 kD. L1CAM can also be cleaved by plasmin resulting in fragments of 140 kD and 80 kD. In theory, therefore, one could detect bands at ~220, 200, 180, 140, 80 and 40 kD.



Our Abpromise guarantee covers the use of ab20148 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

应用 Ab评论 说明
WB Use at an assay dependent concentration. Predicted molecular weight: 200-220 kDa. It may also detect smaller cleavage fragments (please see Notes below).
IP Use at an assay dependent concentration.
IHC-P Use at an assay dependent concentration.


  • 功能Cell adhesion molecule with an important role in the development of the nervous system. Involved in neuron-neuron adhesion, neurite fasciculation, outgrowth of neurites, etc. Binds to axonin on neurons.
  • 疾病相关Defects in L1CAM are the cause of hydrocephalus due to stenosis of the aqueduct of Sylvius (HSAS) [MIM:307000]. Hydrocephalus is a condition in which abnormal accumulation of cerebrospinal fluid in the brain causes increased intracranial pressure inside the skull. This is usually due to blockage of cerebrospinal fluid outflow in the brain ventricles or in the subarachnoid space at the base of the brain. In children is typically characterized by enlargement of the head, prominence of the forehead, brain atrophy, mental deterioration, and convulsions. In adults the syndrome includes incontinence, imbalance, and dementia. HSAS is characterized by mental retardation and enlarged brain ventricles.
    Defects in L1CAM are the cause of mental retardation-aphasia-shuffling gait-adducted thumbs syndrome (MASA) [MIM:303350]; also known as corpus callosum hypoplasia, psychomotor retardation, adducted thumbs, spastic paraparesis, and hydrocephalus or CRASH syndrome. MASA is an X-linked recessive syndrome with a highly variable clinical spectrum. Main clinical features include spasticity and hyperreflexia of lower limbs, shuffling gait, mental retardation, aphasia and adducted thumbs. The features of spasticity have been referred to as complicated spastic paraplegia type 1 (SPG1). Some patients manifest corpus callosum hypoplasia and hydrocephalus. Inter- and intrafamilial variability is very wide, such that patients with hydrocephalus, MASA, SPG1, and agenesis of corpus callosum can be present within the same family.
    Defects in L1CAM are the cause of spastic paraplegia X-linked type 1 (SPG1) [MIM:303350]. Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs.
    Note=Defects in L1CAM may contribute to Hirschsprung disease by modifying the effects of Hirschsprung disease-associated genes to cause intestinal aganglionosis.
    Defects in L1CAM are a cause of partial agenesis of the corpus callosum (ACCPX) [MIM:304100]. A syndrome characterized by partial corpus callosum agenesis, hypoplasia of inferior vermis and cerebellum, mental retardation, seizures and spasticity. Other features include microcephaly, unusual facies, and Hirschsprung disease in some patients.
  • 序列相似性Belongs to the immunoglobulin superfamily. L1/neurofascin/NgCAM family.
    Contains 5 fibronectin type-III domains.
    Contains 6 Ig-like C2-type (immunoglobulin-like) domains.
  • 细胞定位Cell membrane.
  • Information by UniProt
  • 数据库链接
  • 别名
    • Antigen identified by monoclonal antibody R1 antibody
    • CAML1 antibody
    • CD171 antibody
    • CD171 antigen antibody
    • HSAS antibody
    • HSAS1 antibody
    • Hyd antibody
    • L1 antibody
    • L1 cell adhesion molecule antibody
    • L1-NCAM antibody
    • L1cam antibody
    • L1CAM_HUMAN antibody
    • MASA antibody
    • MIC5 antibody
    • N CAML1 antibody
    • N-CAM-L1 antibody
    • NCAM-L1 antibody
    • NCAML1 antibody
    • Nerve-growth factor-inducible large external glycoprotein antibody
    • Neural cell adhesion molecule L1 antibody
    • NILE antibody
    • OTTHUMP00000025992 antibody
    • S10 antibody
    • SPG1 antibody
    see all

Anti-L1CAM antibody [UJ127.11] 图像

  • Anti-L1CAM antibody [UJ127.11] (ab20148) at 5 µg/ml + SK N BE (Human neuroblastoma) Whole Cell Lysate at 10 µg

    Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP at 1/3000 dilution

    Predicted band size : 200-220 kDa
    Observed band size : 200-220 kDa

Anti-L1CAM antibody [UJ127.11] (ab20148)参考文献

This product has been referenced in:
  • Boo YJ  et al. L1 expression as a marker for poor prognosis, tumor progression, and short survival in patients with colorectal cancer. Ann Surg Oncol 14:1703-11 (2007). Read more (PubMed: 17211730) »
  • Patel K  et al. Monoclonal antibody UJ127.11 recognizes the human homologue of mouse L1 cell adhesion molecule. Biochem Soc Trans 18:274 (1990). Read more (PubMed: 2379713) »

See all 3 Publications for this product

Product Wall

Application Immunocytochemistry/ Immunofluorescence
Sample Human Cell (WM3248 melanoma cell line)
Permeabilization No
Specification WM3248 melanoma cell line
Blocking step BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 1% · Temperature: 25°C
Fixative Paraformaldehyde

Dr. Praveen Agrawal

Verified customer

提交于 Mar 24 2017

Abcam guarantees this product to work in the species/application used in this Abreview.
Application Western blot
Sample Human Cell lysate - whole cell (Melanoma)
Gel Running Conditions Reduced Denaturing
Loading amount 20 µg
Specification Melanoma
Blocking step Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C

Abcam user community

Verified customer

提交于 Mar 23 2017

Application Immunoprecipitation
Sample Human Cell lysate - whole cell (Melanoma cell line)
Total protein in input 1000 µg
Immuno-precipitation step Protein G
Specification Melanoma cell line

Abcam user community

Verified customer

提交于 Nov 13 2015

Application Immunohistochemistry (Frozen sections)
Blocking step Serum as blocking agent for 30 minute(s) · Concentration: 10% · Temperature: RT°C
Sample Rhesus monkey Tissue sections (Brain)
Specification Brain
Permeabilization No
Fixative Paraformaldehyde

Abcam user community

Verified customer

提交于 Sep 05 2014

Application Immunocytochemistry/ Immunofluorescence
Blocking step BSA as blocking agent for 30 minute(s) · Concentration: 3% · Temperature: 24°C
Sample Human Cell (Endometrial cancer cell lines: Hec1a and Ishikawa)
Specification Endometrial cancer cell lines: Hec1a and Ishikawa
Permeabilization Yes - Triton 0,1%
Fixative Paraformaldehyde

Ms. Eva Colas

Verified customer

提交于 Jun 19 2014

I can confirm that clone UJ127.11 is the same as UJ127.

Thank you for your enquiry. I have enquired at the originator of the product but unfortunately, we do not have the immunogen information that you want. I am sorry I can't be of more assistance in this occasion but should you need any other info...

Read More

Dear Professor Nikiforov, Thank you for your email and your patience. I have all of the information that you requested. L1CAM can be detected between 200-220 kD. In brain samples it is typically seen at ~ 200 kD. When the protein is overexpres...

Read More