MMADHC Antikörper (AA 1-296)

Produktnummer ABIN7268495

Produktdetails anti-MMADHC Antikörper

Target: MMADHC (Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC))

Bindungsspezifität: AA 1-296

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MMADHC Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Verwendungszweck: MMADHC Rabbit pAb

Sequenz: MANVLCNRAR LVSYLPGFCS LVKRVVNPKA FSTAGSSGSD ESHVAAAPPD ICSRTVWPDE TMGPFGPQDQ RFQLPGNIGF DCHLNGTASQ KKSLVHKTLP DVLAEPLSSE RHEFVMAQYV NEFQGNDAPV EQEINSAETY FESARVECAI QTCPELLRKD FESLFPEVAN GKLMILTVTQ KTKNDMTVWS EEVEIEREVL LEKFINGAKE ICYALRAEGY WADFIDPSSG LAFFGPYTNN TLFETDERYR HLGFSVDDLG CCKVIRHSLW GTHVVVGSIF TNATPDSHIM KKLSGN

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-296 of human MMADHC (NP_056517.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu MMADHC

Target: MMADHC (Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC))

Andere Bezeichnung: MMADHC (MMADHC Produkte)

Synonyme: C2orf25 antikoerper, CL25022 antikoerper, cblD antikoerper, 2010311D03Rik antikoerper, AI314967 antikoerper, RGD1303272 antikoerper, methylmalonic aciduria and homocystinuria, cblD type antikoerper, methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria antikoerper, MMADHC antikoerper, Mmadhc antikoerper

Hintergrund: This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.,MMADHC,C2orf25,CL25022,cblD,cblD type,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,MMADHC

Molekulargewicht: 32kDa

Gen-ID: 27249

UniProt: Q9H3L0