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MITF antibody (AA 1-114)
MITF
Reactivity: Human
WB, IHC, FACS, ELISA, ICC
Host: Mouse
Monoclonal
8F1G5
unconjugated
Product Details anti-MITF Antibody
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Target
See all MITF Antibodies
MITF
(Microphthalmia-Associated Transcription Factor (MITF))
Binding Specificity
All epitopes for MITF antibodies
AA 1-114
Reactivity
All reactivities for MITF antibodies
Human
Host
All hosts for MITF antibodies
Mouse
Clonality
All clonalities for MITF antibodies
Monoclonal
Conjugate
All conjugates for MITF antibodies
This MITF antibody is un-conjugated
Application
All applications for MITF antibodies
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS), ELISA, Immunocytochemistry (ICC)
Immunogen
Purified recombinant fragment of human MITF (AA 1-114) expressed in E. Coli.
Clone
8F1G5
Isotype
IgG1
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Discover our top product MITF Primary Antibody
Alternatives
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Application Details
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Application Notes
ELISA: 1:10000, WB: 1:500 - 1:2000, IHC: , ICC: , FCM: 1:200 - 1:400
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.05 % sodium azide
Storage
4 °C,-20 °C
Storage Comment
4°C, -20°C for long term storage
Target Details for MITF
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Target
MITF
(Microphthalmia-Associated Transcription Factor (MITF))
Alternative Name
MITF (MITF Products )
Synonyms
MITF antibody, ws2a antibody, mitfa antibody, MITF-A antibody, LOC100313655 antibody, mitfb antibody, CMM8 antibody, MI antibody, WS2 antibody, WS2A antibody, bHLHe32 antibody, BCC2 antibody, Bhlhe32 antibody, Gsfbcc2 antibody, Vitiligo antibody, Wh antibody, bw antibody, mi antibody, vit antibody, MITF-H antibody, MITF-M antibody, CMI9 antibody, melanogenesis associated transcription factor antibody, microphthalmia-associated transcription factor antibody, microphthalmia-associated transcription factor S homeolog antibody, Microphthalmia antibody, MITF antibody, mitf antibody, LOC100313655 antibody, mitf.S antibody, LOC100534525 antibody, MICROP antibody, Mitf antibody
Background
This gene encodes a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. It regulates the differentiation and development of melanocytes retinal pigment epithelium and is also responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.,
Molecular Weight
66.2kDa
HGNC
2099
Pathways
Chromatin Binding
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