TPM3 anticorps (Middle Region)
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- Antigène Voir toutes TPM3 Anticorps
- TPM3 (Tropomyosin 3 (TPM3))
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Épitope
- Middle Region
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Reactivité
- Humain, Souris, Rat, Boeuf (Vache), Chien, Cobaye, Cheval, Lapin, Poisson zèbre (Danio rerio)
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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)
- Séquence
- TEERAELAES RCREMDEQIR LMDQNLKCLS AAEEKYSQKE DKYEEEIKIL
- Homologie
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 100%
- Attributs du produit
- This is a rabbit polyclonal antibody against TPM3. It was validated on Western Blot using a cell lysate as a positive control.
- Purification
- Affinity Purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human TPM3
- Top Product
- Discover our top product TPM3 Anticorps primaire
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- Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
- Commentaires
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Antigen size: 285 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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An economic evaluation of atorvastatin for primary prevention of cardiovascular events in type 2 diabetes." dans: PharmacoEconomics, Vol. 26, Issue 4, pp. 329-39, (2008) (PubMed).
: "
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An economic evaluation of atorvastatin for primary prevention of cardiovascular events in type 2 diabetes." dans: PharmacoEconomics, Vol. 26, Issue 4, pp. 329-39, (2008) (PubMed).
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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
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TPM3 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.This gene encodes 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.
Alias Symbols: FLJ41118, MGC14582, MGC3261, MGC72094, NEM1, OK/SW-cl.5, TM-5, TM3, TM30, TM30nm, TPMsk3, TRK, hscp30, TM5, CFTD, hTM5
Protein Interaction Partner: TLK1, MAD1L1, TRIP6, TPM3, TP53, TNNT1, VPS52, TRIM27, PBX3, MAGEA11, KIFC3, KCNE1, IFIT3, HSF2, LURAP1, WASH3P, HDDC3, FAM9C, LCA5L, C1orf216, IKBIP, SYCE1, CCDC114, CCDC102B, KXD1, CCDC146, THAP1, CCHCR1, TFPT, BLOC1S6, OIP5, UBC, MDM2, RNF2, MAGED2, MG
Protein Size: 285 - Poids moléculaire
- 33 kDa
- ID gène
- 7170
- NCBI Accession
- NM_153649, NP_705935
- UniProt
- P06753
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