MMADHC Antikörper (C-Term)
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- Target Alle MMADHC Antikörper anzeigen
- MMADHC (Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC))
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Bindungsspezifität
- AA 226-253, C-Term
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser MMADHC Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Homologie
- M, Rat
- Aufreinigung
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogen
- This MMADHC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 226-253 amino acids from the C-terminal region of human MMADHC.
- Klon
- RB37493
- Isotyp
- Ig Fraction
- Top Product
- Discover our top product MMADHC Primärantikörper
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- Applikationshinweise
- WB: 1:1000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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
- MMADHC Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
- Haltbarkeit
- 6 months
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- 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.
- Molekulargewicht
- 32940
- Gen-ID
- 27249
- NCBI Accession
- NP_056517
- UniProt
- Q9H3L0
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