TPM2 Polyclonal Antibody

SKU: E-AB-16102

Size: 200μL

Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.

Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

Exp date: 12 months

Category ID_II: Primary Antibodies

Category ID_III: Polyclonal Antibodies

Abbreviation: TPM2

Target Synonym: Alpha tropomyosin;AMCD1;Arthrogryposis multiplex congenital distal type 1;Beta tropomyosin;Beta-tropomyosin;Cytoskeletal tropomyosin TM30;DA1;DA2B;epididymis secretory protein Li 273;FLJ41118;Heat stable cytoskeletal protein 30 kDa;HEL-S-273;hscp30;HTM alpha;hTM5;MGC14582;MGC3261;MGC72094;NEM1;NEM4;Nemaline myopathy type 4;OK/SW cl.5;Sarcomeric tropomyosin kappa;TM 5;TM3;TM30;TM30nm;TMSA;TMSB;TPM 1;TPM 3;TPM1 alpha;TPM1 kappa;TPM2;TPM2;TRK;Tropomyosin 1 alpha;Tropomyosin 1 alpha chain;Tropomyosin 1 alpha chain isoform 6;Tropomyosin 2 (beta);Tropomyosin 2;Tropomyosin 3;Tropomyosin alpha 3 chain;Tropomyosin alpha striated muscle isoform;Tropomyosin beta chain;Tropomyosin gamma;Tropomyosin skeletal muscle beta;Tropomyosin-2

Research Areas: Signal Transduction

Conjugation: Unconjugated

Host: Rabbit

Species reactivity: Human;Mouse;Rat

Application: WB;IHC

Isotype: IgG

Clonality: Polyclonal

Clone NO.:

UNIProt ID: P07951

Accession:

Background: This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Concentration: 0.2 mg/mL

Immunogen: Synthetic peptide of human TPM2

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Dilution: WB 1:1000-1:5000;IHC 1:25-1:100

Calculated MW: 33kDa

ObservedMW: