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Thermo Fisher Scientific TPM3 Polyclonal Antibody
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Thermo Fisher Scientific TPM3 Polyclonal Antibody

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TPM3 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot 및 IHC(P)에서 검증됨. Human, Mouse, Rat에 반응하며, 항원 친화 크로마토그래피로 정제됨. PBS/glycerol buffer에 보관되며 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 05. 오후 07:10
Thermo Fisher Scientific PA552644 TPM3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific TPM3 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 0.04–0.4 µg/mL View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human TPM3. Recombinant protein control fragment (Product # RP-89192)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2648847

Product Specific Information

Immunogen sequence:
AERLQREVEG ERRAREQAEA EVASLNRRIQ LVEEELDRAQ ERLATALQKL EEAEKAADES ERGMKVIENR ALKDEEKMEL QEIQLKEAKH IAEEADRKYE EVARKLVIIE GDLERTEERA ELAESRCREM DEQIRLMDQN LKCLSA

Highest antigen sequence identity to the following orthologs:

  • Mouse: 100%
  • Rat: 100%

Target Information

TPM3 (tropomyosin 3) is a member of the tropomyosin family of actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosins are dimers of coiled-coil proteins that polymerize end-to-end along the major groove in most actin filaments. They provide stability to the filaments and regulate access of other actin-binding proteins. In muscle cells, they regulate muscle contraction by controlling the binding of myosin heads to the actin filament. Mutations in this gene result in autosomal dominant nemaline myopathy, and oncogenes formed by chromosomal translocations involving this locus are associated with cancer. Multiple transcript variants encoding different isoforms have been found for this gene.


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

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