Actin Antikörper (AA 3-100) (AbBy Fluor® 488)

Produktnummer ABIN6977308

Produktdetails anti-Actin Antikörper (AbBy Fluor® 488)

Target: Actin

Bindungsspezifität: AA 3-100

Reaktivität: Human, Ratte, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Actin Antikörper ist konjugiert mit AbBy Fluor® 488

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Kreuzreaktivität: Human, Maus, Ratte

Homologie: Dog,Cow,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human ACTA1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu Actin

Target: Actin

Abstract: Actin Produkte

Synonyme: Act57 antikoerper, Act57A antikoerper, Act57b antikoerper, Actin antikoerper, BEST:RE38067 antikoerper, C antikoerper, CG10067 antikoerper, CG30294 antikoerper, Dmel\\CG10067 antikoerper, M antikoerper, T10 antikoerper, act 57A antikoerper, act57A antikoerper, act57B antikoerper, act57b antikoerper, actin antikoerper, anon-EST:CL2c12 antikoerper, 143060_f_at antikoerper, CG7478 antikoerper, D antikoerper, Dmel\\CG7478 antikoerper, act 79B antikoerper, act79B antikoerper, mus79B antikoerper, Act(88F) antikoerper, Act88-F antikoerper, Act88f antikoerper, CG5178 antikoerper, Dmel\\CG5178 antikoerper, E antikoerper, Ifm(3)7 antikoerper, act 88F antikoerper, act88F antikoerper, rsd antikoerper, Act87e antikoerper, CG18290 antikoerper, Dmel\\CG18290 antikoerper, act 87E antikoerper, act87E antikoerper, mus87E antikoerper, Act88F antikoerper, Dsim\\GD19025 antikoerper, GD19025 antikoerper, dsim_GLEANR_2829 antikoerper, 42A antikoerper, A antikoerper, AFFX-Dros-ACTIN_M_r_at antikoerper, Act antikoerper, Act42 antikoerper, Act42a antikoerper, Actin/BAP47 antikoerper, BAP47 antikoerper, CG12051 antikoerper, Dmel\\CG12051 antikoerper, act 42A antikoerper, act42A antikoerper, cytoplasmic antikoerper, Actin 57B antikoerper, Actin 79B antikoerper, Actin 88F antikoerper, Actin 87E antikoerper, Actin-like protein C08B11.6 antikoerper, hypothetical protein antikoerper, ACT_COLSC Actin (ISS) antikoerper, Actin 42A antikoerper, actin gamma 1 antikoerper, actin antikoerper, Actin, gamma 1 antikoerper, si:ch211-241j12.3 antikoerper, Act57B antikoerper, Act79B antikoerper, Act88F antikoerper, Act87E antikoerper, arp-6 antikoerper, Dsim\Act88F antikoerper, ACTIN antikoerper, Act42A antikoerper, ACTG1 antikoerper, LOC548170 antikoerper, Bm1_16810 antikoerper, IDA5 antikoerper, LOC100342017 antikoerper, si:ch211-241j12.3 antikoerper

Hintergrund:

Synonyms: muscle Actin, ACTS_HUMAN, Actin, alpha skeletal muscle, Alpha-actin-1, ACTA1, ACTA, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3, Actin alpha skeletal muscle, actin, alpha 1, skeletal muscle 1, actin, alpha 1, skeletal muscle, actina, aktin, alpha Actin 1, alpha skeletal muscle Actin, alpha skeletal muscle, alpha-actin, Beta cytoskeletal actin, nemaline myopathy type 3.

Background: The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects. [provided by RefSeq, Jul 2008]

Gen-ID: 58

UniProt: P68133