MITF (D5G7V) Rabbit Monoclonal Antibody#12590,Cell Signaling Technology (CST),12590

MITF (D5G7V) Rabbit Monoclonal Antibody recognizes endogenous levels of total MITF protein. This antibody is predicted to recognize all known isoforms of MITF. Based on sequence similarities and testing with exogenously expressed TFE3 samples, this antibody may also detect the related MiT/TEF protein family member TFE3.

Host

Rabbit

Reactivity

Human, Mouse, Rat, Hamster, Monkey

Application

Western Blotting: 1:1000 Chromatin IP: 1:50 Chromatin IP-seq: 1:50

Platform ID

BAB800084035

Cell Signaling Technology (CST)

Headquarters

3 Trask Lane Danvers, MA 01923

Contact

Tel: 877-616-2355,978-867-2388
Fax: 877-616-2355

Product Specifications
Scientific Background
Synonyms

Specifications

NameMITF (D5G7V) Rabbit Monoclonal Antibody#12590
Cat. No.12590
Accession NumberO75030
Gene ID (Entrez)75030, 4286
HostRabbit
SensitivityEndogenous
ReactivityHuman, Mouse, Rat, Hamster, Monkey
ApplicationWestern Blotting: 1:1000 Chromatin IP: 1:50 Chromatin IP-seq: 1:50
Molecular Weight50-75
ImmunogenIgG
FormulationFor optimal ChIP and ChIP-seq results, use 10 μl of antibody and 10 μg of chromatin (approximately 4 x 106cells) per IP. This antibody has been validated using SimpleChIP®Enzymatic Chromatin IP Kits.
StorageSupplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Regulatory StatusResearch Use Only

Scientific Background

Microphthalmia-associated transcription factor (MITF) is a basic helix-loop-helix leucine zipper transcription factor that is most widely known for its roles in melanocyte, ophthalmic, and osteoclast development (1-3). In humans, MITF can function as a melanoma oncogene (4) and mutations in the correspondingMITFgene are associated with Waardenburg syndrome type 2, an auditory-pigmentary syndrome characterized by developmental defects in cells derived from neural crest (5). At least 12 isoforms of MITF have been identified, which exhibit differential patterns of expression among cell and tissue types (6).Hershey, C.L. and Fisher, D.E. (2004)Bone34, 689-96.Nomura, S. et al. (2001)J Bone Miner Metab19, 183-7.Widlund, H.R. and Fisher, D.E. (2003)Oncogene22, 3035-41.Levy, C. et al. (2006)Trends Mol Med12, 406-14.Read, A.P. and Newton, V.E. (1997)J Med Genet34, 656-65.Tachibana, M. (2000)Pigment Cell Res13, 230-40.Alternate NamesBHLHE32; Class E basic helix-loop-helix protein 32; CMM8; COMMAD; homolog of mouse microphthalmia; melanocyte inducing transcription factor; melanogenesis associated transcription factor; MI; microphtalmia-associated transcription factor; Microphthalmia-associated transcription factor; microphthalmia-associated transcription factor-M transcript; MITF; WS2; WS2A

Synonyms

BHLHE32; Class E basic helix-loop-helix protein 32; CMM8; COMMAD; homolog of mouse microphthalmia; melanocyte inducing transcription factor; melanogenesis associated transcription factor; MI; microphtalmia-associated transcription factor; Microphthalmia-associated transcription factor; microphthalmia-associated transcription factor-M transcript; MITF; WS2; WS2A

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