Recombinatie MiTF monoklonaal antilichaam

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.

MITF

O75030

Human; Mouse; Rat

Recombinant Human MiTF protein

CMM; bHLHe; MITF; CMM8; COMMAD; MI; WS2; WS2A; bHLHe32

2C7

Unconjugated

WB; IHC

Epigenetics and Nuclear Signaling; Immunology

Protein A

0.2 mg/mL

IHC 1:200-500; WB 1:1000-5000

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/JjKCTZi5

58 kDa

58 kDa

IgG, κ