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MITF antibody (N-Term)
MITF
Reactivity: Human
WB, IF, FACS, EIA
Host: Rabbit
Polyclonal
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 8-36, N-Term
Reactivity
All reactivities for MITF antibodies
Human
Host
All hosts for MITF antibodies
Rabbit
Clonality
All clonalities for MITF antibodies
Polyclonal
Conjugate
All conjugates for MITF antibodies
This MITF antibody is un-conjugated
Application
All applications for MITF antibodies
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)
Specificity
This antibody recognizes Human MITF (N-term).
Purification
Protein A column, followed by peptide affinity purification
Immunogen
KLH conjugated synthetic peptide between 8-36 amino acids from the N-terminal region of Human MITF.
Isotype
Ig Fraction
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Discover our top product MITF Primary Antibody
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS containing 0.09 % (W/V) Sodium Azide as preservative
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Target Details for MITF
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Target
MITF
(Microphthalmia-Associated Transcription Factor (MITF))
Alternative Name
MITF (MITF Products )
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.Synonyms: Mi-protein, Microphthalmia-associated transcription factor
Molecular Weight
58795 Da
Gene ID
4286
NCBI Accession
NP_000239
Pathways
Chromatin Binding
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