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Laminin

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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. Activates presynaptic signaling involving integrin alpha-PS3/beta-nu and Fak to suppress neuromuscular junction (NMJ) growth during larval development and during low crawling activity, but not during higher-crawling conditions. Mediates, together with integrin alpha-PS3/beta-nu, glutamate receptor-modulated NMJ growth.

Below are the list of possible Laminin products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Laminin subunit alpha

 Laminin subunit alpha ELISA Kit
 Laminin subunit alpha Recombinant
 Laminin subunit alpha Antibody
Also known as Laminin subunit alpha (Laminin A chain).
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. Activates presynaptic signaling involving integrin alpha-PS3/beta-nu and Fak to suppress neuromuscular junction (NMJ) growth during larval development and during low crawling activity, but not during higher-crawling conditions. Mediates, together with integrin alpha-PS3/beta-nu, glutamate receptor-modulated NMJ
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growth.
 LanA ELISA Kit
 LanA Recombinant
 LanA Antibody
 lamA ELISA Kit
 lamA Recombinant
 lamA Antibody
 CG10236 ELISA Kit
 CG10236 Recombinant
 CG10236 Antibody
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Laminin subunit alpha-1

 Laminin subunit alpha-1 ELISA Kit
 Laminin subunit alpha-1 Recombinant
 Laminin subunit alpha-1 Antibody
Also known as Laminin subunit alpha-1 (Laminin A chain) (Laminin-1 subunit alpha) (Laminin-3 subunit alpha) (S-laminin subunit alpha) (S-LAM alpha).
LAMA1: 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.

Prot
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ein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 18p11.3

Cellular Component: basement membrane; extracellular matrix; extracellular region; extracellular space; laminin-1 complex; laminin-3 complex; proteinaceous extracellular matrix

Molecular Function: extracellular matrix structural constituent; protein binding

Biological Process: cell surface receptor linked signal transduction; extracellular matrix organization and biogenesis

Disease: Poretti-boltshauser Syndrome
 LAMA1 ELISA Kit
 LAMA1 Recombinant
 LAMA1 Antibody
 LAMA ELISA Kit
 LAMA Recombinant
 LAMA Antibody
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Laminin subunit alpha-2

 Laminin subunit alpha-2 ELISA Kit
 Laminin subunit alpha-2 Recombinant
 Laminin subunit alpha-2 Antibody
Also known as Laminin subunit alpha-2 (Laminin M chain) (Laminin-12 subunit alpha) (Laminin-2 subunit alpha) (Laminin-4 subunit alpha) (Merosin heavy chain).
LAMA2: 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. De
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fects in LAMA2 are the cause of merosin-deficient congenital muscular dystrophy type 1A (MDC1A). MDC1A is characterized by difficulty walking, hypotonia, proximal weakness, hyporeflexia, and white matter hypodensity on MRI.

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 6q22-q23

Cellular Component: basement membrane; extracellular matrix; extracellular region

Molecular Function: structural molecule activity

Biological Process: extracellular matrix organization and biogenesis; muscle development

Disease: Muscular Dystrophy, Congenital Merosin-deficient, 1a
 LAMA2 ELISA Kit
 LAMA2 Recombinant
 LAMA2 Antibody
 LAMM ELISA Kit
 LAMM Recombinant
 LAMM Antibody
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Laminin subunit alpha-3

 Laminin subunit alpha-3 ELISA Kit
 Laminin subunit alpha-3 Recombinant
 Laminin subunit alpha-3 Antibody
Also known as Laminin subunit alpha-3 (Epiligrin 170 kDa subunit) (E170) (Epiligrin subunit alpha) (Kalinin subunit alpha) (Laminin-5 subunit alpha) (Laminin-6 subunit alpha) (Laminin-7 subunit alpha) (Nicein subunit alpha).
LAMA3: Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic develo
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pment by interacting with other extracellular matrix components. Defects in LAMA3 are a cause of epidermolysis bullosa junctional Herlitz type (H-JEB); also known as junctional epidermolysis bullosa Herlitz-Pearson type. JEB defines a group of blistering skin diseases characterized by tissue separation which occurs within the dermo-epidermal basement membrane. H-JEB is a severe, infantile and lethal form. Death occurs usually within the first six months of life. Occasionally, children survive to teens. H-JEB is marked by bullous lesions at birth and extensive denudation of skin and mucous membranes that may be hemorrhagic. Defects in LAMA3 are the cause of laryngoonychocutaneous syndrome (LOCS). LOCS is an autosomal recessive epithelial disorder confined to the Punjabi Muslim population. The condition is characterized by cutaneous erosions, nail dystrophy and exuberant vascular granulation tissue in certain epithelia, especially conjunctiva and larynx. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 18q11.2

Cellular Component: basement membrane; extracellular region

Biological Process: epidermis development; extracellular matrix disassembly; extracellular matrix organization and biogenesis; hemidesmosome assembly

Disease: Epidermolysis Bullosa, Junctional, Herlitz Type; Epidermolysis Bullosa, Junctional, Non-herlitz Type; Laryngoonychocutaneous Syndrome
 LAMA3 ELISA Kit
 LAMA3 Recombinant
 LAMA3 Antibody
 LAMNA ELISA Kit
 LAMNA Recombinant
 LAMNA Antibody
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Laminin subunit alpha-4

 Laminin subunit alpha-4 ELISA Kit
 Laminin subunit alpha-4 Recombinant
 Laminin subunit alpha-4 Antibody
Also known as Laminin subunit alpha-4 (Laminin-14 subunit alpha) (Laminin-8 subunit alpha) (Laminin-9 subunit alpha).
LAMA4: 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. 3 isoforms of the human protein are produc
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ed by alternative splicing.

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 6q21

Cellular Component: basal lamina; basement membrane; extracellular matrix; extracellular region

Molecular Function: extracellular matrix structural constituent; protein binding

Biological Process: extracellular matrix organization and biogenesis

Disease: Cardiomyopathy, Dilated, 1jj
 LAMA4 ELISA Kit
 LAMA4 Recombinant
 LAMA4 Antibody
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Laminin subunit alpha-5

 Laminin subunit alpha-5 ELISA Kit
 Laminin subunit alpha-5 Recombinant
 Laminin subunit alpha-5 Antibody
Also known as Laminin subunit alpha-5 (Laminin-10 subunit alpha) (Laminin-11 subunit alpha) (Laminin-15 subunit alpha).
LAMA5: 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.

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 20q13.2-q13.3

Cellular Component: basement membrane; extracellular matrix; ext
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racellular region; extracellular space; laminin-10 complex; nucleus

Molecular Function: integrin binding; structural molecule activity

Biological Process: cell migration; extracellular matrix organization and biogenesis; integrin-mediated signaling pathway
 LAMA5 ELISA Kit
 LAMA5 Recombinant
 LAMA5 Antibody
 KIAA0533 ELISA Kit
 KIAA0533 Recombinant
 KIAA0533 Antibody
 KIAA1907 ELISA Kit
 KIAA1907 Recombinant
 KIAA1907 Antibody
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Laminin subunit B

 Laminin subunit B ELISA Kit
 Laminin subunit B Recombinant
 Laminin subunit B Antibody
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 ext
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racellular matrix components.
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Laminin subunit beta-1

 Laminin subunit beta-1 ELISA Kit
 Laminin subunit beta-1 Recombinant
 Laminin subunit beta-1 Antibody
Also known as Laminin subunit beta-1 (Fragments).
Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues durin
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g embryonic development by interacting with other extracellular matrix components.
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Laminin subunit beta-1 variant

 Laminin subunit beta-1 variant ELISA Kit
 Laminin subunit beta-1 variant Recombinant
 Laminin subunit beta-1 variant Antibody
Also known as Laminin subunit beta-1 variant (Laminin beta-1-2 chain).
Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cel
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ls into tissues during embryonic development by interacting with other extracellular matrix components.
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Laminin subunit beta-2

 Laminin subunit beta-2 ELISA Kit
 Laminin subunit beta-2 Recombinant
 Laminin subunit beta-2 Antibody
Also known as Laminin subunit beta-2 (Laminin B1s chain) (Laminin-11 subunit beta) (Laminin-14 subunit beta) (Laminin-15 subunit beta) (Laminin-3 subunit beta) (Laminin-4 subunit beta) (Laminin-7 subunit beta) (Laminin-9 subunit beta) (S-laminin subunit beta) (S-LAM beta).
LAMB2: Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organizat
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ion of cells into tissues during embryonic development by interacting with other extracellular matrix components. Defects in LAMB2 are the cause of Pierson syndrome (PIERSS); also known as microcoria-congenital nephrotic syndrome. Pierson syndrome is characterized by nephrotic syndrome with neonatal onset, diffuse mesangial sclerosis and eye abnormalities with microcoria as the leading clinical feature. Death usually occurs within the first weeks of life. Disease severity depends on the mutation type: nontruncating LAMB2 mutations may display variable phenotypes ranging from a milder variant of Pierson syndrome to isolated congenital nephrotic syndrome. Defects in LAMB2 are the cause of nephrotic syndrome type 5 with or without ocular abnormalities (NPHS5). NPHS5 is a renal disease characterized clinically by proteinuria, hypoalbuminemia, hyperlipidemia and edema. Kidney biopsies show non-specific histologic changes such as focal segmental glomerulosclerosis and diffuse mesangial proliferation. Some affected individuals have an inherited steroid-resistant form and progress to end-stage renal failure. NPHS5 is characterized by very early onset of progressive renal failure. A subset of patients may develop mild ocular anomalies, such as myopia, nystagmus, and strabismus.

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 3p21

Cellular Component: basal lamina; basement membrane; extracellular matrix; extracellular region; laminin-3 complex

Biological Process: extracellular matrix organization and biogenesis

Disease: Nephrotic Syndrome, Type 5, With Or Without Ocular Abnormalities; Pierson Syndrome
 LAMB2 ELISA Kit
 LAMB2 Recombinant
 LAMB2 Antibody
 LAMS ELISA Kit
 LAMS Recombinant
 LAMS Antibody
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Laminin subunit beta-3

 Laminin subunit beta-3 ELISA Kit
 Laminin subunit beta-3 Recombinant
 Laminin subunit beta-3 Antibody
Also known as Laminin subunit beta-3 (Epiligrin subunit bata) (Kalinin B1 chain) (Kalinin subunit beta) (Laminin B1k chain) (Laminin-5 subunit beta) (Nicein subunit beta).
LAMB3: 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. Defects in LAMB3 are a cause of epidermolysis bullosa junctional Herlitz type (H-JEB); also known as junctional epidermolysis bullosa Herlitz-Pearson type. JEB defines a group of blistering skin diseases characterized by tissue separation which occurs within the dermo-epidermal basement membrane. H-JEB is a severe, infantile and lethal form. Death occurs usually within the first six months of life. Occasionally, children survive to teens. H-JEB is marked by bullous lesions at birth and extensive denudation of skin and mucous membranes that may be hemorrhagic. Defects in LAMB3 are a cause of generalized atrophic benign epidermolysis bullosa (GABEB). GABEB is a non- lethal, adult form of junctional epidermolysis bullosa characterized by life-long blistering of the skin, associated with hair and tooth abnormalities.

Protein type: Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 1q32

Cellular Component: extracellular region

Molecular Function: protein binding

Biological Process: epidermis development; extracellular matrix disassembly; extracellular matrix organization and biogenesis; hemidesmosome assembly

Disease: Amelogenesis Imperfecta, Type Ia; Epidermolysis Bullosa, Junctional, Herlitz Type; Epidermolysis Bullosa, Junctional, Non-herlitz Type
 LAMB3 ELISA Kit
 LAMB3 Recombinant
 LAMB3 Antibody
 LAMNB1 ELISA Kit
 LAMNB1 Recombinant
 LAMNB1 Antibody
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Laminin subunit beta-4

 Laminin subunit beta-4 ELISA Kit
 Laminin subunit beta-4 Recombinant
 Laminin subunit beta-4 Antibody
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.
 lamb4 ELISA Kit
 lamb4 Recombinant
 lamb4 Antibody
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Laminin subunit gamma-1

 Laminin subunit gamma-1 ELISA Kit
 Laminin subunit gamma-1 Recombinant
 Laminin subunit gamma-1 Antibody
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.
 lamc1 ELISA Kit
 lamc1 Recombinant
 lamc1 Antibody
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Laminin subunit gamma-2

 Laminin subunit gamma-2 ELISA Kit
 Laminin subunit gamma-2 Recombinant
 Laminin subunit gamma-2 Antibody
Also known as Laminin subunit gamma-2 (Cell-scattering factor 140 kDa subunit) (CSF 140 kDa subunit) (Epiligrin subunit gamma) (Kalinin subunit gamma) (Kalinin/nicein/epiligrin 100 kDa subunit) (Ladsin 140 kDa subunit) (Laminin B2t chain) (Laminin-5 subunit gamma) (Large adhesive scatter factor 140 kDa subunit) (Nicein subunit gamma).
LAMC2: 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. Ladsin exerts cell- sca
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ttering activity toward a wide variety of cells, including epithelial, endothelial, and fibroblastic cells. Defects in LAMC2 are a cause of epidermolysis bullosa junctional Herlitz type (H-JEB); also known as junctional epidermolysis bullosa Herlitz-Pearson type. JEB defines a group of blistering skin diseases characterized by tissue separation which occurs within the dermo-epidermal basement membrane. H-JEB is a severe, infantile and lethal form. Death occurs usually within the first six months of life. Occasionally, children survive to teens. H-JEB is marked by bullous lesions at birth and extensive denudation of skin and mucous membranes that may be hemorrhagic. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 1q25-q31

Cellular Component: extracellular region

Biological Process: epidermis development; extracellular matrix disassembly; extracellular matrix organization and biogenesis; hemidesmosome assembly; positive regulation of cell migration; positive regulation of cell proliferation

Disease: Epidermolysis Bullosa, Junctional, Herlitz Type; Epidermolysis Bullosa, Junctional, Non-herlitz Type
 LAMC2 ELISA Kit
 LAMC2 Recombinant
 LAMC2 Antibody
 LAMB2T ELISA Kit
 LAMB2T Recombinant
 LAMB2T Antibody
 LAMNB2 ELISA Kit
 LAMNB2 Recombinant
 LAMNB2 Antibody
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Laminin subunit gamma-3

 Laminin subunit gamma-3 ELISA Kit
 Laminin subunit gamma-3 Recombinant
 Laminin subunit gamma-3 Antibody
Also known as Laminin subunit gamma-3 (Laminin-12 subunit gamma) (Laminin-14 subunit gamma) (Laminin-15 subunit gamma).
LAMC3: 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. Defects in LAMC3 are the cause of cortic
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al malformations occipital (OCCM). OCCM is a disease in which affected individuals develop seizures, sometimes associated with transient visual changes. Brain MRI shows both pachygyria and polymicrogyria restricted to the lateral occipital lobes.

Protein type: Extracellular matrix; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 9q34.12

Cellular Component: extracellular region; membrane; proteinaceous extracellular matrix

Molecular Function: structural molecule activity

Biological Process: extracellular matrix organization and biogenesis

Disease: Cortical Malformations, Occipital
 LAMC3 ELISA Kit
 LAMC3 Recombinant
 LAMC3 Antibody
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