![MITF antibody [C5]](https://www.genetex.com/upload/website/prouct_img/normal/GTX12039/MiTF-antibody-C5-GTX12039-IHC-p-1_w_23060519_824.webp)
GTX12039
MITF antibody [C5]
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX12039
- Zusätzliche Namen:
- melanocyte inducing transcription factor , CMM8 , COMMAD , MI , WS2 , WS2A , bHLHe32
- Anwendung:
- WB, IHC-P, IHC-Fr, IP
- Konzentration:
- 1 mg/ml
- Physischer Zustand:
- Liquid
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Protein G Purified
- Lagerbedingungen:
- -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.
- Hersteller:
- Genetex
- Host:
- Mouse
- Reaktivitäten:
- Human, Mouse, Rat
- Buffer:
- PBS, 0.08% Sodium azide.
- Immunogen:
- N-terminal fragment of human microphthalmia protein and mouse myeloma NS1 cells.
- Klon:
- C5
- Uniprot:
- O75030
- Synonyme:
- 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
- Weitere Details:
- The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is 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. [provided by RefSeq, Aug 2017]
- Versandbedingungen:
- Blue Ice