ELMOD3 Antikörper (AA 290-381)

Produktnummer ABIN7266922

Produktdetails anti-ELMOD3 Antikörper

Target: ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))

Bindungsspezifität: AA 290-381

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ELMOD3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Verwendungszweck: ELMOD3 Rabbit pAb

Sequenz: ATFLHLAHVW RTQRKTISDS GFVLKELEVL AKKSPRRLLK TLELYLARVS KGQASLLGAQ KCYGPEAPPF KDLTFTGESD LQSHSSEGVW LI

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 290-381 of human ELMOD3 (NP_001128493.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ELMOD3

Target: ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))

Andere Bezeichnung: ELMOD3 (ELMOD3 Produkte)

Synonyme: LST3 antikoerper, RBED1 antikoerper, RBM29 antikoerper, AI844780 antikoerper, C330008I15Rik antikoerper, Rbed1 antikoerper, Kcmf1 antikoerper, ELMO domain containing 3 antikoerper, ELMO/CED-12 domain containing 3 antikoerper, ELMOD3 antikoerper, Elmod3 antikoerper

Hintergrund: This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded protein is found in stereocilia, kinocilia and cuticular plate of developing hair cells suggesting a function for this protein in cochlear sensory cells. An allelic variant of this family has been associated with autosomal recessive nonsyndromic deafness-88 in humans. Alternative splicing results in multiple transcript variants.,ELMOD3,DFNB88,LST3,RBED1,RBM29,Signal Transduction,G protein signaling,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Endocrine & Metabolism,ELMOD3

Molekulargewicht: 18kDa/20kDa/28kDa/43kDa/44kDa

Gen-ID: 84173

UniProt: Q96FG2