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Thermo Fisher Scientific Microphthalmia Transcription Factor (MITF) Recombinant Rabbit Monoclonal Antibody (MITF/2987R)
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Thermo Fisher Scientific Microphthalmia Transcription Factor (MITF) Recombinant Rabbit Monoclonal Antibody (MITF/2987R)

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MITF 단백질을 표적으로 하는 Thermo Fisher Scientific의 재조합 토끼 단일클론 항체로, 인간 및 개 시료에 반응합니다. IHC, ICC/IF, Flow Cytometry 등 다양한 응용에 적합하며, Protein A/G 정제된 액상 형태로 제공됩니다. 연구용으로만 사용됩니다.

카탈로그번호
4286-RBM5-Px (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 04. 오후 04:19
Thermo Fisher Scientific 4286-RBM5-P1 Microphthalmia Transcription Factor (MITF) Recombinant Rabbit Monoclonal Antibody (MITF/2987R) 100 ug pk판매 단위 pk ·
재고 확인 필요
1,063,800원VAT 포함 1,170,180원
Thermo Fisher Scientific 4286-RBM5-P0 Microphthalmia Transcription Factor (MITF) Recombinant Rabbit Monoclonal Antibody (MITF/2987R) 20 ug pk판매 단위 pk ·
재고 확인 필요
532,500원VAT 포함 585,750원

Thermo Fisher Scientific · Thermo Fisher Scientific Microphthalmia Transcription Factor (MITF) Recombinant Rabbit Monoclonal Antibody (MITF/2987R)

Applications and Tested Dilutions

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL
Immunocytochemistry (ICC/IF) 1–2 µg/mL
Flow Cytometry (Flow) 1–2 µg/10^6 cells

Product Specifications

Specification Description
Species Reactivity Dog, Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone MITF/2987R
Immunogen Recombinant full-length human MiTF protein
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C, do not freeze
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Does not react with Mouse or Rat

Target Information

Mi (Microphthalmia Transcription Factor, MITF) is a basic helix-loop-helix-leucine zipper (b-HLH-ZIP) transcription factor involved in pigmentation, mast cell function, and bone development.
Mutations in Mi cause Waardenburg Syndrome type II in humans. In mice, loss of Mi leads to absence of pigmented cells in skin, eyes, and inner ear, as well as osteopetrosis and defects in natural killer and mast cells.
Two isoforms exist, differing by 66 amino acids at the N-terminus.

  • Shorter forms: expressed in melanocytes, observed as two bands at 52 kDa and 56 kDa.
  • Longer forms: expressed in osteoclasts, B16 melanoma cells, mast cells, and heart, appearing as clusters at 60–70 kDa.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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