MID1 Antikörper (C-Term)

Produktnummer ABIN2775948

Produktdetails anti-MID1 Antikörper

Target: MID1 (Midline 1 (MID1))

Bindungsspezifität: C-Term

Reaktivität: Human, Maus, Ratte, Hund, Rind (Kuh), Meerschweinchen, Pferd, Zebrafisch (Danio rerio)

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MID1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: AINQAGSRSS EPGKLKTNSQ PFKLDPKSAH RKLKVSHDNL TVERDESSSK

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

Produktmerkmale: This is a rabbit polyclonal antibody against MID1. It was validated on Western Blot using a cell lysate as a positive control.

Aufreinigung: Protein A purified

Immunogen: The immunogen is a synthetic peptide directed towards the C terminal region of human MID1

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 667 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: 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.

Details zu MID1

Target: MID1 (Midline 1 (MID1))

Andere Bezeichnung: MID1 (MID1 Produkte)

Hintergrund: MID1 is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Several different transcript variants are generated by alternate splicing, however, the full length nature of two variants has not been determined.
Alias Symbols: OS, FXY, OSX, OGS1, XPRF, BBBG1, GBBB1, MIDIN, RNF59, ZNFXY, TRIM18
Protein Interaction Partner: STK36, MID2, UBE2E3, DYRK4, UBE2E2, UBE2E1, UBE2D3, UBE2D2, UBE2D1, PKN1, PPP2R4, PPP2CA, MID1, MEOX1, FKBP1A, EHHADH, BYSL, TCEANC, UBTD1, OTUB2, GMCL1, HTT, IGBP1, PNKP, MID1IP1, GNB2L1, RPS8, RPS3, NPM1, HSP90AA1, EEF1A1, ANXA2, UBC, UBE2D4, UBE2N, ELA
Protein Size: 667

Molekulargewicht: 75 kDa

Gen-ID: 4281

NCBI Accession: NM_000381, NP_000372

UniProt: O15344