Tropomyosin anticorps (N-Term)

N° du produit ABIN2776783

Détail du produit anti-Tropomyosin anticorps

Antigène: Tropomyosin (TPM1) (Tropomyosin 1 (Alpha) (TPM1))

Épitope: N-Term

Reactivité: Humain, Rat, Souris, Poisson zèbre (Danio rerio), Lapin, Boeuf (Vache), Chien, Cheval, Cobaye, Mouton

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Tropomyosin est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Séquence: DRAEQAEADK KAAEDRSKQL EDELVSLQKK LKGTEDELDK YSEALKDAQE

Homologie: Cow: 93%, Dog: 100%, Guinea Pig: 100%, Horse: 93%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Sheep: 93%, Zebrafish: 100%

Attributs du produit: This is a rabbit polyclonal antibody against TPM1. It was validated on Western Blot and immunohistochemistry.

Purification: Protein A purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human TPM1

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 284 AA

Restrictions: For Research Use only

Stockage

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.

Détails sur Tropomyosin

Antigène: Tropomyosin (TPM1) (Tropomyosin 1 (Alpha) (TPM1))

Autre désignation: TPM1 (TPM1 Produits)

Synonymes: anticorps alpha-fTM, anticorps Tm7, anticorps tpm1, anticorps MGC84844, anticorps AA986836, anticorps AI854628, anticorps TM2, anticorps Tm3, anticorps Tmpa, anticorps Tpm-1, anticorps alpha-TM, anticorps Alpha-tm, anticorps Tma2, anticorps Tmsa, anticorps TPM1, anticorps fb37a09, anticorps tm, anticorps wu:fb37a09, anticorps CH1, anticorps alpha-tm, anticorps alpha-tropomyosin, anticorps C15orf13, anticorps CMD1Y, anticorps CMH3, anticorps HTM-alpha, anticorps TMSA, anticorps TPMA, anticorps Tm1, anticorps zgc:171719, anticorps zgc:55951, anticorps zgc:77009, anticorps tropomyosin 1 (alpha), anticorps tropomyosin, anticorps tropomyosin 1, anticorps tropomyosin 1, alpha, anticorps alpha-tropomyosin, anticorps tropomyosin 1 L homeolog, anticorps TPM1, anticorps tm7, anticorps Tpm1, anticorps tpma, anticorps tpm1.L, anticorps Smp_044010.2, anticorps LOC732984, anticorps tpm1

Sujet: TPM1 is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction.This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy.
Alias Symbols: CMH3, TMSA, TPM1-alpha, CMD1Y, C15orf13, HTM-alpha
Protein Interaction Partner: GOLGA2, CAGE1, C1orf216, SYCE1, KXD1, TFPT, MAD1L1, TPM4, TP53, TNNT1, UBC, MDM2, ETFA, FOXK1, KIAA1598, PPP6R3, APPL2, CDC37, MGEA5, STUB1, ABI2, DNAJC7, HSP90B1, PARK2, LRCH3, PAN2, TGFBR1, SPTBN1, ATF2, MDC1, BRCA1, PPP4R2, SRXN1, NUDCD2, RBM15, THOC2,
Protein Size: 284

Poids moléculaire: 31 kDa

ID gène: 7168

NCBI Accession: NM_000366, NP_000357

UniProt: P09493

Pathways: Regulation of Actin Filament Polymerization