Antibody data
- Antibody Data
- Antigen structure
- References [5]
- Comments [0]
- Validations [0]
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- Product number
- ABIN401289 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Diaphanous Homolog 2 (Drosophila) (DIAPH2) (AA 1085-1101), (Isoform 2) antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide corresponding aa 1085-1101 of Human DIA-2
- Description
- Affinity chromatography
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Epitope
- AA 1085-1101,Isoform 2
- Isotype
- IgG
- Vial size
- 0.1 mg
- Concentration
- 1.4 mg/mL (by UV absorbance at 280 nm)
- Storage
- -20°C
- Handling
- Avoid repeated freezing and thawing.
Submitted references Identification and characterization of human FMNL1, FMNL2 and FMNL3 genes in silico.
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility.
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21.
Physical mapping of DNA markers in the q13-q22 region of the human X chromosome.
Katoh M, Katoh M
International journal of oncology 2003 May;22(5):1161-8
International journal of oncology 2003 May;22(5):1161-8
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility.
Bione S, Sala C, Manzini C, Arrigo G, Zuffardi O, Banfi S, Borsani G, Jonveaux P, Philippe C, Zuccotti M, Ballabio A, Toniolo D
American journal of human genetics 1998 Mar;62(3):533-41
American journal of human genetics 1998 Mar;62(3):533-41
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.
Lynch ED, Lee MK, Morrow JE, Welcsh PL, León PE, King MC
Science (New York, N.Y.) 1997 Nov 14;278(5341):1315-8
Science (New York, N.Y.) 1997 Nov 14;278(5341):1315-8
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21.
Sala C, Arrigo G, Torri G, Martinazzi F, Riva P, Larizza L, Philippe C, Jonveaux P, Sloan F, Labella T, Toniolo D
Genomics 1997 Feb 15;40(1):123-31
Genomics 1997 Feb 15;40(1):123-31
Physical mapping of DNA markers in the q13-q22 region of the human X chromosome.
Philippe C, Cremers FP, Chery M, Bach I, Abbadi N, Ropers HH, Gilgenkrantz S
Genomics 1993 Jul;17(1):147-52
Genomics 1993 Jul;17(1):147-52
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