TEX261 Antikörper (AA 121-196)

Produktnummer ABIN1386683

Der Kaninchen Polyklonal Anti-TEX261-Antikörper wurde für ELISA, IHC (p), ICC, IF (cc), IF (p) und IHC (fro) validiert. Er ist geeignet, TEX261 in Proben von Human zu detektieren.

Kurzübersicht für TEX261 Antikörper (AA 121-196) (ABIN1386683)

Target: TEX261 (Testis Expressed 261 (TEX261))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TEX261 Antikörper ist unkonjugiert

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

Produktdetails anti-TEX261 Antikörper

Bindungsspezifität: AA 121-196

Homologie: Human,Dog,Cow,Sheep,Pig,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TEX261

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 TEX261

Target: TEX261 (Testis Expressed 261 (TEX261))

Andere Bezeichnung: TEX261

Hintergrund:

Synonyms: 3110001O07Rik, AA409339, AI480706, AL033351, Protein TEX261, TEG 261, TEX261, TX261_HUMAN, UNQ1882/PRO4325.

Background: TEX261 is a 196 amino acid multi-pass membrane protein that belongs to the SVP26 family. The gene that encodes TEX261 consists of approximately 47,406 bases and maps to human chromosome 2p13.3. Consisting of 237 million bases, Chromosome 2 encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is due to mutations in the ALMS1 gene.