Melanoma (HMB45)
Melanomasome

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Antigen Preparation
The cell membrane extract from meloma cell lines of SK-MEL.
Background
Anti-HMB45 is a useful melanoma immunohistochemical marker that reacts with antigenspresent on immature melanosomes. Anti-HMB45 is useful for identifying amelanoticmelanoma from other neoplastic lesions with similar morphology. Melanosomes, the pigment granules that provide tissues with colour and photoprotection, are the cellular site of synthesis, storage and transport of melanin pigments. They are synthesised in mammalian skin melanocytes, in choroidal melanocytes and retinal pigment epithelial (RPE) cells in the eye, and in melanophores (a class of pigment-containing cells) in lower vertebrates. Although melanosomes are considered to be lysosome-related organelles, recent data show that their contents derive from early endosomal membranes. Disorders of pigmentation were among the first genetic diseases ever recognized because of their visually striking clinical phenotypes, resulting from defects of pigmentary melanocytes. These diseases may be most usefully considered as abnormalities of melanocyte development, function, or survival.
PURIFICATION
The mouse IgG is purified by Protein A-Affinity Chromatography according to Isotyping
SPECIFICITY
FORMULATION
This affinity purified antibody is supplied in sterile Phosphate buffered saline (pH7.2) containing antibody stabilizer.
STORAGE
The antibodies are stable for 12 months from date of receipt when stored at –20oC. The antibodies can be stored at 2oC-8oC for one month without detectable loss of activity. Avoid repeated freezing-thawing cycles.
Gene ID
6490
Applications/Suggested Working Dilutions
Western Blot
0.1-1 µg/ml
ELISA
0.01-0.1 µg/ml
Immunoprecipitation
2-5 µg/ml
IHC
2-10 µg/ml
Flow cytometry
5-10 µg/ml
Order Info
Catalog #: 604-920
Lot #:
Size: 100ug/200ul
Host: Mouse
Clone: HMB45
Isotyping: IgG1
Applications: IHC(P), FC
Reactivity: Hu
Price: $ 245.00
REFERENCES
Wasmeier C, et al. (2008) J Cell Sci. 121 (pt24): 3995–3999 Spritz RA et al.. (2003) Curr. Opin. Genet. Dev. 13:284–289 Raposo G, Marks MS (2007). Nat Rev Mol Cell Biol. 8 (10): 786–797
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