TPM3 anticorps
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- Antigène Voir toutes TPM3 Anticorps
- TPM3 (Tropomyosin 3 (TPM3))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp TPM3 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein of human TPM3 (NP_689476.2).
- Isotype
- IgG
- Top Product
- Discover our top product TPM3 Anticorps primaire
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- Indications d'application
- WB 1:500-1:2000 IF 1:50-1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- TPM3 (Tropomyosin 3 (TPM3))
- Autre désignation
- TPM3 (TPM3 Produits)
- Synonymes
- anticorps CAPM1, anticorps CFTD, anticorps NEM1, anticorps OK/SW-cl.5, anticorps TM-5, anticorps TM3, anticorps TM30, anticorps TM30nm, anticorps TM5, anticorps TPMsk3, anticorps TRK, anticorps hscp30, anticorps cb674, anticorps fa17b11, anticorps fb83b01, anticorps fk41e01, anticorps hm:zeh0298, anticorps wu:fa17b11, anticorps wu:fb83b01, anticorps wu:fk41e01, anticorps zeh0298, anticorps zgc:77592, anticorps TPM3, anticorps Tm5NM, anticorps Tpm-5, anticorps Tpm5, anticorps Trop-5, anticorps gamma-TM, anticorps hTM30nm, anticorps hTMnm, anticorps tm3, anticorps tpm3, anticorps tpm3.L, anticorps tropomyosin 3, anticorps tropomyosin 3, gamma, anticorps tropomyosin 3 S homeolog, anticorps TPM3, anticorps tpm3, anticorps Tpm3, anticorps tpm3.S
- Sujet
- This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants.
- Poids moléculaire
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Observed_MW: 38 kDa
Calculated_MW: 18 kDa/28 kDa/29 kDa/32 kDa
- ID gène
- 7170
- UniProt
- P06753
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