Labelling Review row-Online

Primary Antibodies
MDM2 Protein
Clone 1B10
1 mL, 0.1 mL lyophilized NCL-MDM2 F P (HIER)
The human phosphoprotein homolog of the murine double minute 2 (MDM2)
gene, with a molecular weight of 90 kD (p90), forms a complex with both
mutant and wild type p53 protein. The MDM2 gene product interacts with
p53 protein inhibiting p53-mediated transactivation. Overexpression of
MDM2 overcomes wild type p53 mediated suppression of transformed cell
growth. MDM2 amplification is reported to be observed in some soft tissue
sarcomas, osteosarcomas and high grade malignant gliomas.
Product Specific Information
NCL-MDM2 reacts with the human homolog of MDM2.
Human breast carcinoma: immunohistochemical staining for MDM2 protein using NCL-MDM2.
Note nuclear staining of tumor cells. Paraffin sectiion.
Melan A
Clone A103
1 mL, 0.1 mL lyophilized NCL-MelanA F P (HIER) W
1 mL liquid NCL-L-MelanA F P (HIER) W
7 mL ready-to-use RTU-MelanA F P (HIER)
7 mL Bond ready-to-use PA0233 P (HIER)
Melan A, a product of the MART-1 gene, is a melanocyte differentiation
marker recognized by autologous cytotoxic T lymphocytes. Other
melanoma-associated markers recognized by autologous cytotoxic T cells
are reported to include MAGE-1, MAGE-3, tyrosinase, gp100, gp75, BAGE-1
and GAGE-1. The analysis of these different molecules and their expression
in individual melanomas may be of help in the study of their particular
molecular roles in melanocyte differentiation and tumorigenesis.
Refer to page 33 for the Bond ready-to-use format.
Human melanoma: immunohistochemical staining for melan A using NCL-MelanA.
Note cytoplasmic staining of melanoma cells. Paraffin section.
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Reference Range
Melanoma Marker (CD63)
Clone NKI/C3
1 mL, 0.1 mL lyophilized NCL-CD63 FP
See also CD63 (Melanoma Marker) on page 82.
Melanoma Marker (HMB45)
Clone HMB45
1 mL, 0.1mL lyophilized NCL-HMB45 F P (Enzyme)
See also HMB45 (Melanoma Marker) on page 120.
Merosin Laminin Alpha 2 Chain
Clone Mer3/22B2
1 mL lyophilized NCL-MEROSIN F
The dystrophin-glycoprotein complex is localized to the muscle membrane.
Several members of this complex are reported to be implicated in muscular
dystrophy. Dystrophin expression is altered in Duchenne and Becker
muscular dystrophy and four types of limb girdle muscular dystrophy are
caused by mutations in the genes for alpha, beta, gamma and deltasarcoglycan.
An extracellular member of this complex is alpha-dystroglycan
and linked to this, in the extracellular matrix, is laminin. The muscle specific
form of laminin, merosin, is composed of three chains: alpha 2, beta 1 and
gamma 1. Mutations in the chromosome 6 encoded gene for the laminin
alpha 2 chain of merosin are responsible for a form of congenital muscular
dystrophy (CMD). Merosin negative CMD is characterized by a severe
clinical phenotype and is associated with white matter changes on brain
imaging.
Product Specific Information
NCL-MEROSIN reacts with the 300 kD fragment of merosin (Sewry et al.
Muscle and Nerve Supplement. 7, S109: (1998)) labeling with an antibody to
beta-spectrin to monitor membrane integrity, is an essential immunohistochemical
control.
A B
Human skeletal muscle: immunohistochemical staining for merosin using NCL-MEROSIN.
Note membrane staining of normal muscle fibers (A) and absence of staining of muscle fibers
in an individual with chromosome 6-linked congenital muscular dystrophy (B). Frozen sections.
Photographs supplied courtesy of Dr Louise V B Anderson.
Products in this catalog are subject to regulatory approval.
This catalog is not for use in the USA.
Reference Range