Millipore Sigma Vibrant Logo

AB4139 Anti-MITF Antibody

AB4139
100 µg  
Retrieving price...
Price could not be retrieved
Minimum Quantity is a multiple of
Maximum Quantity is
Upon Order Completion More Information
You Saved ()
 
Request Pricing
Limited Availability
Limited Availability
In Stock 
Discontinued
Limited Quantities Available
Availability to be confirmed
    Remaining : Will advise
      Remaining : Will advise
      Will advise
      Contact Customer Service
      Contact Customer Service

      Special Offers

       

      Contact Customer Service

      Overview

      Replacement Information

      Key Spec Table

      Species ReactivityKey ApplicationsHostFormatAntibody Type
      H, M, RICCRbAffinity PurifiedPolyclonal Antibody
      Description
      Catalogue NumberAB4139
      Brand Family Chemicon®
      Trade Name
      • Chemicon
      DescriptionAnti-MITF Antibody
      Alternate Names
      • Microphthalmia-associated Transcription Factor
      References
      Product Information
      FormatAffinity Purified
      PresentationAffinity purified immunoglobulin precipitated in a solution of 50% saturated ammonium sulfate and PBS containing no preservatives.
      Applications
      ApplicationUse Anti-MITF Antibody (Rabbit Polyclonal Antibody) validated in ICC to detect MITF also known as Microphthalmia-associated Transcription Factor.
      Key Applications
      • Immunocytochemistry
      Application NotesImmunocytochemistry: 1/200 to 1/1000.

      Optimal dilutions must be determined by the user.
      Biological Information
      ImmunogenSynthetic peptide corresponding to amino acids 54-63 of human MITF (PNQPGDHVMP).
      HostRabbit
      SpecificityRecognizes MITF. The calculated molecular weight is ~46.9 kDa.
      Species Reactivity
      • Human
      • Mouse
      • Rat
      Antibody TypePolyclonal Antibody
      Entrez Gene Number
      Entrez Gene SummaryThis 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.
      Gene Symbol
      • MITF
      • WS2A
      UniProt Number
      UniProt SummaryFUNCTION: SwissProt: O75030 # Transcription factor for tyrosinase and tyrosinase- related protein 1. Binds to a symmetrical DNA sequence (E-boxes) (5'-CACGTG-3') found in the tyrosinase promoter. Plays a critical role in the differentiation of various cell types as neural crest- derived melanocytes, mast cells, osteoclasts and optic cup-derived retinal pigment epithelium.
      SIZE: 526 amino acids; 58795 Da
      SUBUNIT: Efficient DNA binding requires dimerization with another bHLH protein. Binds DNA in the form of homodimer or heterodimer with either TFE3, TFEB or TFEC.
      SUBCELLULAR LOCATION: Nucleus.
      TISSUE SPECIFICITY: Isoform M is exclusively expressed in melanocytes and melanoma cells. Isoform A and isoform H are widely expressed in many cell types including melanocytes and retinal pigment epithelium (RPE). Isoform C is expressed in many cell types including RPE but not in melanocyte-lineage cells.
      PTM: Phosphorylation at Ser-405 significantly enhances the ability to bind the tyrosinase promoter.
      DISEASE: SwissProt: O75030 # Defects in MITF are the cause of Waardenburg syndrome type IIa (WS2A) [MIM:193510]. It is a dominant inherited disorder characterized by sensorineural hearing loss and patches of depigmentation. The features show variable expression and penetrance. & Defects in MITF are a cause of Waardenburg syndrome type II with ocular albinism (WS2-OA) [MIM:103470]. It is an ocular albinism with sensorineural deafness. & Defects in MITF are the cause of Tietz syndrome [MIM:103500]. It is an autosomal dominant disorder characterized by generalized hypopigmentation and profound, congenital, bilateral deafness. Penetrance is complete.
      SIMILARITY: SwissProt: O75030 ## Contains 1 basic helix-loop-helix (bHLH) domain.
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Usage Statement
      • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
      Storage and Shipping Information
      Storage ConditionsMaintain unopened vial at -20°C for up to 6 months. Avoid repeated freeze/thaw cycles.

      The rehydrated antibody solutions can be stored undiluted at 2-8°C for 2 months without any significant loss of activity. Note, the solution is not sterile, thus care should be taken if product is stored at 2-8°C.

      For storage at -20°C, the addition of an equal volume of glycerol can be used, however, it is recommended that ACS grade or higher glycerol be used, as significant loss of activity can occur if the glycerol used is not of high quality.

      For freezing, it is recommended that the rehydrated antibody solution be further diluted 1:1 with a 2% BSA (fraction V, highest-grade available) solution made with the rehydration buffer. The resulting 1% BSA/antibody solution can be aliquoted and stored frozen at -70°C for up to 6 months. Avoid repeated freeze/thaw cycles.

      PREPARATION AND USE:

      To reconstitute the antibody, centrifuge the antibody vial at moderate speed (5,000 rpm) for 5 minutes to pellet the precipitated antibody product. Carefully remove the ammonium sulfate/PBS buffer solution and discard. It is not necessary to remove all of the ammonium sulfate/PBS solution: 10 μL of residual ammonium sulfate solution will not effect the resuspension of the antibody. Do not let the protein pellet dry, as severe loss of antibody reactivity can occur.

      Resuspend the antibody pellet in any suitable biological buffer, standard PBS or TBS (pH 7.3-7.5) are typical. Volumes required are not critical but it is suggested that the final antibody concentration be between 0.1 mg/mL and 1.0 mg/mL. For example, to achieve a1 mg/mL concentration with 50 μg of precipitated antibody, the amount of buffer needed would be 50 μL.

      Carefully add the liquid buffer to the pellet. DO NOT VORTEX. Mix by gentle stirring with a wide pipet tip or gentle finger-tapping. Let the precipitated antibody rehydrate for 1 hour at 4-25°C prior to use. Small particles of precipitated antibody that fail to resuspend are normal. Vials are overfilled to compensate for any losses.
      Packaging Information
      Material Size100 µg
      Transport Information
      Supplemental Information
      Specifications
      Global Trade ITEM Number
      Catalogue Number GTIN
      AB4139 04053252508653

      Related Products & Applications

      Related Products

      Catalogue Number Description  
      MAB3747-I Anti-Microphthalmia (Mi) Antibody, clone C5 Show Pricing & Availability
      MABE78 Anti-MiTF Antibody, clone 3D1.2 Show Pricing & Availability

      Categories

      Life Science Research > Antibodies and Assays > Primary Antibodies