GJB2 Antikörper (C-Term)

Produktnummer ABIN544540

Produktdetails anti-GJB2 Antikörper

Target: GJB2 (Gap Junction Protein, beta 2, 26kDa (GJB2))

Bindungsspezifität: C-Term

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GJB2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Verwendungszweck: Rabbit polyclonal antibody raised against synthetic peptide of GJB2.

Kreuzreaktivität: Human, Maus

Immunogen: A synthetic peptide (conjugated with KLH) corresponding to C-terminus of human GJB2.

Anwendungsinformationen

Applikationshinweise: Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:50-100)
Western Blot (1:1000)
The optimal working dilution should be determined by the end user.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: In PBS (0.09 % sodium azide)

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.

Referenzen für anti-GJB2 Antikörper (ABIN544540)

Alesutan, Sopjani, Munoz, Fraser, Kemp, Föller, Lang: "Inhibition of connexin 26 by the AMP-activated protein kinase." in: The Journal of membrane biology, Vol. 240, Issue 3, pp. 151-8, (2011) (PubMed).

Ohtsuka, Yuge, Kimura, Namba, Abe, Van Laer, Van Camp, Usami: "GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation." in: Human genetics, Vol. 112, Issue 4, pp. 329-33, (2003) (PubMed).

Yotsumoto, Hashiguchi, Chen, Ohtake, Tomitaka, Akamatsu, Matsunaga, Shiraishi, Miura, Adachi, Kanzaki: "Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome." in: The British journal of dermatology, Vol. 148, Issue 4, pp. 649-53, (2003) (PubMed).

Uyguner, Tukel, Baykal, Eris, Emiroglu, Hafiz, Ghanbari, Baserer, Yuksel-Apak, Wollnik: "The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family." in: Clinical genetics, Vol. 62, Issue 4, pp. 306-9, (2002) (PubMed).

Details zu GJB2

Target: GJB2 (Gap Junction Protein, beta 2, 26kDa (GJB2))

Andere Bezeichnung: GJB2 / Cx26 (GJB2 Produkte)

Synonyme: ppk antikoerper, cx26 antikoerper, dfna3 antikoerper, dfnb1 antikoerper, nsrd1 antikoerper, dfna3a antikoerper, dfnb1a antikoerper, MGC53062 antikoerper, connexin-26 antikoerper, GJB2 antikoerper, AI325222 antikoerper, Cnx26 antikoerper, Cx26 antikoerper, Gjb-2 antikoerper, CXN-26 antikoerper, CX26 antikoerper, DFNA3 antikoerper, DFNA3A antikoerper, DFNB1 antikoerper, DFNB1A antikoerper, HID antikoerper, KID antikoerper, NSRD1 antikoerper, PPK antikoerper, gap junction protein beta 2 L homeolog antikoerper, gap junction protein beta 2 antikoerper, gap junction protein, beta 2 antikoerper, gjb2.L antikoerper, GJB2 antikoerper, Gjb2 antikoerper

Gen-ID: 2706

Pathways: Sensory Perception of Sound, Cell-Cell Junction Organization