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Mouse Anti-LAMA1 Recombinant Antibody (3H11) (CBMAB-0186-CN)

This product is a mouse antibody that recognizes LAMA1 of chicken. The antibody 3H11 can be used for immunoassay techniques such as: IF, WB.
See all LAMA1 antibodies

Summary

Host Animal
Mouse
Specificity
Chicken, Avian
Clone
3H11
Antibody Isotype
IgG1, κ
Application
IF, WB

Basic Information

Immunogen
Retinal basal laminae (E10)
Specificity
Chicken, Avian
Antibody Isotype
IgG1, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Purity
>95%, as determined by SDS-PAGE analysis
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
laminin, alpha 1
Introduction
This gene encodes one of the alpha 1 subunits of laminin. The laminins are a family of extracellular matrix glycoproteins that have a heterotrimeric structure consisting of an alpha, beta and gamma chain. These proteins make up a major component of the basement membrane and have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Mutations in this gene may be associated with Poretti-Boltshauser syndrome.
Entrez Gene ID
374016
UniProt ID
F1NM47
Alternative Names
LAMA1
Function
Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.
Biological Process
Animal organ morphogenesisManual Assertion Based On ExperimentIBA:GO_Central
Axon guidanceManual Assertion Based On ExperimentIBA:GO_Central
Blood vessel morphogenesisManual Assertion Based On ExperimentIBA:GO_Central
Branching involved in salivary gland morphogenesisIEA:Ensembl
Camera-type eye developmentManual Assertion Based On ExperimentIBA:GO_Central
Cell adhesionIEA:UniProtKB-KW
Cell surface receptor signaling pathwayISS:UniProtKB
Epithelial tube branching involved in lung morphogenesisIEA:Ensembl
Establishment of epithelial cell apical/basal polarityIEA:Ensembl
Morphogenesis of an epithelial sheetIEA:Ensembl
Protein phosphorylationIEA:Ensembl
Regulation of cell adhesionIEA:InterPro
Regulation of cell migrationIEA:InterPro
Regulation of embryonic developmentIEA:InterPro
Retinal blood vessel morphogenesisIEA:Ensembl
Tissue developmentManual Assertion Based On ExperimentIBA:GO_Central
Cellular Location
Secreted, extracellular space, extracellular matrix, basement membrane
Major component.
Involvement in disease
Poretti-Boltshauser syndrome (PTBHS):
An autosomal recessive disorder characterized by cerebellar dysplasia, cerebellar vermis atrophy, cerebellar cysts in most patients, high myopia, variable retinal dystrophy, and eye movement abnormalities including strabismus, ocular apraxia, nystagmus. Affected individuals have ataxia, delayed motor development, language impairment, and intellectual disability with variable severity.
PTM
Tyrosine phosphorylated by PKDCC/VLK.

Wang, P., Jia, X., Xiao, X., Li, S., Long, Y., Liu, M., ... & Zhang, Q. (2021). An early diagnostic clue for COL18A1-and LAMA1-associated diseases: high myopia with alopecia areata in the cranial midline. Frontiers in Cell and Developmental Biology, 9, 644947.

Powell, L., Olinger, E., Wedderburn, S., Ramakumaran, V. S., Kini, U., Clayton-Smith, J., ... & Sayer, J. A. (2021). Identification of LAMA1 mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndrome. Brain Communications, 3(3), fcab163.

Zhou, P. L., Wu, Z., Zhang, W., Xu, M., Ren, J., Zhang, Q., ... & Han, X. (2021). Circular RNA hsa_circ_0000277 sequesters miR-4766-5p to upregulate LAMA1 and promote esophageal carcinoma progression. Cell death & disease, 12(7), 676.

Kurek, M., Åkesson, E., Yoshihara, M., Oliver, E., Cui, Y., Becker, M., ... & Stukenborg, J. B. (2021). Spermatogonia loss correlates with LAMA 1 expression in human prepubertal testes stored for fertility preservation. Cells, 10(2), 241.

Chen, M., Zhang, M., Qian, Y., Yang, Y., Sun, Y., Liu, B., ... & Dong, M. (2020). Identification of a likely pathogenic structural variation in the LAMA1 gene by Bionano optical mapping. NPJ genomic medicine, 5(1), 31.

Elmas, M., Gogus, B., & Solak, M. (2020). Understanding what you have found: a family with a mutation in the LAMA1 gene with literature review. Clinical Medicine Insights: Case Reports, 13, 1179547620948666.

Biler, E. D., Ilim, O., Palamar, M., Onay, H., & Uretmen, O. (2018). TGFB1 and LAMA1 gene polymorphisms in children with high myopia. Pakistan journal of medical sciences, 34(2), 463.

Marlow, E., Chan, R. P., Oltra, E., Rusu, I., & Gupta, M. P. (2018). Retinal avascularity and neovascularization associated with LAMA1 (laminin1) mutation in Poretti-Boltshauser syndrome. JAMA ophthalmology, 136(1), 96-97.

Kashevarova, A. A., Nazarenko, L. P., Skryabin, N. A., Nikitina, T. V., Vasilyev, S. A., Tolmacheva, E. N., ... & Lebedev, I. N. (2018). A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11. 32 microduplication in a patient with keratosis pilaris and intellectual disability. American Journal of Medical Genetics Part A, 176(11), 2395-2403.

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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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