ARG41334

anti-MITF antibody

anti-MITF antibody for Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes MITF
Tested Reactivity Hu, Ms
Tested Application WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name MITF
Antigen Species Human
Immunogen Recombinant fusion protein corresponding to aa. 1-280 of Human MITF (NP_937801.1).
Conjugation Un-conjugated
Alternate Names bHLHe32; Class E basic helix-loop-helix protein 32; MI; Microphthalmia-associated transcription factor; WS2; WS2A; CMM8

Application Instructions

Application Suggestion
Tested Application Dilution
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Mouse kidney
Observed Size ~ 58 kDa

Properties

Form Liquid
Purification Affinity purified.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 17342 Mouse MITF

GeneID: 4286 Human MITF

Swiss-port # O75030 Human Microphthalmia-associated transcription factor

Swiss-port # Q08874 Mouse Microphthalmia-associated transcription factor

Gene Symbol MITF
Gene Full Name microphthalmia-associated transcription factor
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. [provided by RefSeq, Jul 2008]
Function Transcription factor that regulates the expression of genes with essential roles in cell differentiation, proliferation and survival. Binds to symmetrical DNA sequences (E-boxes) (5'-CACGTG-3') found in the promoters of target genes, such as BCL2 and tyrosinase (TYR). Plays an important role in melanocyte development by regulating the expression of tyrosinase (TYR) and tyrosinase-related protein 1 (TYRP1). Plays a critical role in the differentiation of various cell types, such as neural crest-derived melanocytes, mast cells, osteoclasts and optic cup-derived retinal pigment epithelium. [UniProt]
Cellular Localization Nucleus. [UniProt]
Calculated MW 59 kDa
PTM Phosphorylation at Ser-405 significantly enhances the ability to bind the tyrosinase promoter. Phosphorylated at Ser-180 and Ser-516 following KIT signaling, trigerring a short live activation: Phosphorylation at Ser-180 and Ser-516 by MAPK and RPS6KA1, respectively, activate the transcription factor activity but also promote ubiquitination and subsequent degradation by the proteasome.

Ubiquitinated following phosphorylation at Ser-180, leading to subsequent degradation by the proteasome. Deubiquitinated by USP13, preventing its degradation. [UniProt]

Images (1) Click the Picture to Zoom In

  • ARG41334 anti-MITF antibody WB image

    Western blot: 25 µg of Mouse kidney lysate stained with ARG41334 anti-MITF antibody at 1:1000 dilution.