ABIN952395
antibody from antibodies-online
Targeting: FTSJ1
CDLIV, JM23, MRX44, MRX9, SPB1, TRM7, TRMT7
Antibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations
- Western blot [1]
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- Product number
- ABIN952395 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-FtsJ RNA Methyltransferase Homolog 1 (E. Coli) (FTSJ1) (AA 1-30), (N-Term) antibody
- Antibody type
- Polyclonal
- Description
- Protein A column, followed by peptide affinity purification
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- N-Term, AA 1-30
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references Positive association of the FTSJ1 gene polymorphisms with nonsyndromic X-linked mental retardation in young Chinese male subjects.
Genetic variations in FTSJ1 influence cognitive ability in young males in the Chinese Han population.
A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family.
hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes.
Dai L, Xing L, Gong P, Zhang K, Gao X, Zheng Z, Zhou J, Guo Y, Guo S, Zhang F
Journal of human genetics 2008;53(7):592-7
Journal of human genetics 2008;53(7):592-7
Genetic variations in FTSJ1 influence cognitive ability in young males in the Chinese Han population.
Gong P, Li J, Dai L, Zhang K, Zheng Z, Gao X, Zhang F
Journal of neurogenetics 2008;22(4):277-87
Journal of neurogenetics 2008;22(4):277-87
A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family.
Takano K, Nakagawa E, Inoue K, Kamada F, Kure S, Goto Y, Japanese Mental Retardation Consortium.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Jun 5;147B(4):479-84
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Jun 5;147B(4):479-84
hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes.
Lamesch P, Li N, Milstein S, Fan C, Hao T, Szabo G, Hu Z, Venkatesan K, Bethel G, Martin P, Rogers J, Lawlor S, McLaren S, Dricot A, Borick H, Cusick ME, Vandenhaute J, Dunham I, Hill DE, Vidal M
Genomics 2007 Mar;89(3):307-15
Genomics 2007 Mar;89(3):307-15
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- Experimental details
- WB