![MITF antibody [21D1418]](https://www.genetex.com/upload/website/prouct_img/normal/GTX13703/GTX13703_990_WB_w_23060620_374.webp)
![MITF antibody [21D1418]](https://www.genetex.com/upload/website/prouct_img/normal/GTX13703/GTX13703_991_WB_w_23060620_949.webp)
GTX13703
MITF antibody [21D1418]
Cannot supply to this region.
- SKU:
- GTX13703
- Additional Names:
- melanocyte inducing transcription factor , CMM8 , COMMAD , MI , WS2 , WS2A , bHLHe32
- Application:
- WB, IHC-P, IF, ICC
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Protein G Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Mouse
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- PBS, 0.02% Sodium Azide.
- Immunogen:
- A synthetic peptide derived from human MITF(Accession O75030), corresponding to amino acid 300~350.
- Clone:
- 21D1418
- Uniprot:
- O75030
- Synonyms:
- bHLHe32;class E basic helix-loop-helix protein 32;CMM8;COMMAD;melanogenesis associated transcription factor;MI;microphtalmia-associated transcription factor;microphthalmia-associated transcription factor;MITF-A;WS2;WS2A
- Extra Details:
- 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]
- Shipping Conditions:
- Blue Ice