EMID1 Antikörper (AA 351-441)

Produktnummer ABIN6943246

Der Kaninchen Polyklonal anti-EMID1 Antikörper wird verwendet zum Nachweis von EMID1 in Proben von Human. Er wurde validiert für IF (cc), IF (p), IHC (fro) und IHC (p).

Kurzübersicht für EMID1 Antikörper (AA 351-441) (ABIN6943246)

Target: EMID1 (EMI Domain Containing 1 (EMID1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser EMID1 Antikörper ist unkonjugiert

Applikation: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Produktdetails anti-EMID1 Antikörper

Bindungsspezifität: AA 351-441

Verwendungszweck: EMID1 Polyclonal Antibody

Kreuzreaktivität: Ratte

Homologie: Human,Mouse,Dog,Cow

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human EMID1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu EMID1

Target: EMID1 (EMI Domain Containing 1 (EMID1))

Andere Bezeichnung: EMID1

Hintergrund:

Synonyms: AW122071, CO 5, CTA-984G1.2, EMI domain containing 1, EMI domain containing protein 1, EMI domain-containing protein 1, EMI5, EMID 1, Emid1, EMID1_HUMAN, Emilin and multimerin domain containing protein 1, Emilin and multimerin domain-containing protein 1, EMU1, hEmu1, MGC50657, OTTMUSP00000005297, Protein Emu1, Putative emu1, RGD1565846, RP23-338J18.3.

Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

Gen-ID: 129080

UniProt: Q96A84