TYRP1 recombinant monoclonal antibody, clone TA99
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More Files
- More Functions
Flow Cytometry
Flow-cytometry analysis of TYRP1 in mouse splenocytes, B16F10 murine melanoma cells, KPC3 pacreas carcinoma cells, KPC3 cells transfected with the Trp1 gene using human anti-TRP1 (TA99) recombinant monoclonal antibody, clone TA99 (Cat # RAB03918).
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Specification
Product Description
Rabbit recombinant monoclonal antibody raised against 70-75 kDa pigmentation-associated glycoprotein in human melanoma cell lines.
Antibody Species
Rabbit
Immunogen
Original antibody is raised against recombinant protein corresponding to 70-75 kDa pigmentation-associated glycoprotein in human melanoma cell lines.
Reactivity
Human
Form
Liquid
Isotype
IgG
Recommend Usage
ELISA
Flow cytometry
Immunofluorescence
Immunohistochemistry (Frozen sections)
Immunoprecipitation
Western Blot
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.02% Proclin 300)
Storage Instruction
Store at 4°C for 3 months. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing. -
Applications
Western Blot
Immunohistochemistry (Frozen sections)
Immunofluorescence
Immunoprecipitation
Enzyme-linked Immunoabsorbent Assay
Flow Cytometry
Flow-cytometry analysis of TYRP1 in mouse splenocytes, B16F10 murine melanoma cells, KPC3 pacreas carcinoma cells, KPC3 cells transfected with the Trp1 gene using human anti-TRP1 (TA99) recombinant monoclonal antibody, clone TA99 (Cat # RAB03918). -
Gene Info — TYRP1
Entrez GeneID
7306Protein Accession#
P17643Gene Name
TYRP1
Gene Alias
CAS2, CATB, GP75, TRP, TYRP, b-PROTEIN
Gene Description
tyrosinase-related protein 1
Gene Ontology
HyperlinkGene Summary
This gene encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Defects in this gene are the cause of rufous oculocutaneous albinism and oculocutaneous albinism type III. [provided by RefSeq
Other Designations
associated with iris pigmentation
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Interactome
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Pathway
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Disease
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