TMEM252 Antikörper (AA 31-130) (HRP)
-
- Target Alle TMEM252 Produkte
- TMEM252 (Transmembrane Protein 252 (TMEM252))
- Bindungsspezifität
- AA 31-130
- Reaktivität
- Human
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser TMEM252 Antikörper ist konjugiert mit HRP
-
Applikation
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))
- Homologie
- Human,Mouse,Rat,Dog,Pig,Horse
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C9orf71
- Isotyp
- IgG
-
-
- Applikationshinweise
-
IHC-P 1:200-400
IHC-F 1:100-500 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Handhabung
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
-
- Target
- TMEM252 (Transmembrane Protein 252 (TMEM252))
- Andere Bezeichnung
- C9orf71 (TMEM252 Produkte)
- Synonyme
- C9orf71 antikoerper, RP11-274B18.1 antikoerper, E030010A14Rik antikoerper, RGD1359349 antikoerper, transmembrane protein 252 antikoerper, TMEM252 antikoerper, Tmem252 antikoerper
- Hintergrund
-
Synonyms: C9orf71, Chromosome 9 open reading frame 71, TM252_HUMAN, MGC34760, RP11-274B18.1, TMEM252, Transmembrane protein 252, Transmembrane protein C9orf71.
Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf71 gene product has been provisionally designated C9orf71 pending further characterization.
- Gen-ID
- 169693
-