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當(dāng)前位置:首頁 > 抗原抗體、ELISA、WB > 一抗 > Monoclonal Antibodies > Microphthalmia Transcription Factor (MITF) Antibody - Without BSA and Azide

Microphthalmia Transcription Factor (MITF) Antibody - Without BSA and Azide

貨號 貨期 規(guī)格 / 價格 詢價
AMM01045G 100 μg / ¥4950

Microphthalmia Transcription Factor (MITF) Antibody - Without BSA and Azide

品牌

Leading Biology

貨號

AMM01045G

產(chǎn)品分類

Monoclonal Antibodies

研究領(lǐng)域

產(chǎn)品概述

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality Microphthalmia Transcription Factor (MITF) Antibody - Without BSA and Azide.

分子量

52-56kDa (doublet)

細胞定位

Antigen Cellular Localization: Nucleus.

宿主

Mouse

種屬反應(yīng)性

Human

克隆號

SPM290

亞型

Mouse / IgG1, kappa

通用名

BHLHE32

基因ID

UniProt ID

功能

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.

總結(jié)

MITF (microphthalmia transcription factor) is a basic helix-loop-helix-leucine-zipper (bHLH-Zip) transcription factor that regulates the development and survival of melanocytes and retinal pigment epithelium, and also is involved in transcription of pigmentation enzyme genes such as tyrosinase TRP1 and TRP2. MITF has been shown to be phosphorylated by MAP kinase in response to c-kit activation, resulting in upregulation of MITF transcriptional activity. Mutations of the MITF gene are associated with the autosomal dominant hereditary deafness and pigmentation condition, Waardenburg Syndrome type 2A. Multiple isoforms of MITF exist, including MITF-A, MITF-B, MITF-C, MITF-H, and MITF-M, which differ in the amino-terminal domain and in their expression patterns. The MITF-M isoform is restricted to the melanocyte cell lineage. Anti-MITF, D5, recognizes a nuclear protein, which is expressed in the majority of primary and metastatic epithelioid malignant melanomas as well as in normal melanocytes, benign nevi and dysplastic nevi.

形式

Liquid

儲存條件

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

應(yīng)用

IHC, IF, FC

圖像

Formalin-fixed, paraffin-embedded human Melanoma stained with MITF Monoclonal Antibody (SPM290).

說明書

數(shù)量

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