CXX1 Antikörper (AA 121-209)

Produktnummer ABIN6942745

Der Kaninchen Polyklonal Anti-CXX1 Antikörper wurde für IF (p), ELISA, IF (cc), IHC (p), IHC (fro) und ICC validiert. Er ist geeignet, CXX1 in Proben von Human zu detektieren.

Kurzübersicht für CXX1 Antikörper (AA 121-209) (ABIN6942745)

Target: CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CXX1 Antikörper ist unkonjugiert

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

Produktdetails anti-CXX1 Antikörper

Bindungsspezifität: AA 121-209

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Cerebral protein 5/CXX1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

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 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu CXX1

Target: CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))

Andere Bezeichnung: CXX1

Hintergrund:

Synonyms: Cerebral protein 5, CAAX box protein 1, CXX 1, FAM127A, Family with sequence similarity 127, member A, Mammalian retrotransposon derived protein 8C, Mar8, MAR8C, Mart8, MART8C, CXX1_HUMAN.

Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXX1 gene product has been provisionally designated CXX1 pending further characterization.

Gen-ID: 8933

UniProt: A6ZKI3