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ImmunohistochemistryAntibody data
- Antibody Data
- Antigen structure
- References [12]
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- Product number
- HPA028305 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA028305, RRID:AB_10601807
- Product name
- Anti-DNALI1
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human DNALI1, Gene description: dynein, axonemal, light intermediate chain 1, Alternative Gene Names: dJ423B22.5, hp28, P28, Validated applications: IHC, Uniprot ID: O14645, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.1 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review
A novel mutation in PCD‐associated gene DNAAF3 causes male infertility due to asthenozoospermia
Identification of a novel splice site mutation in the DNAAF4 gene of a Chinese patient with primary ciliary dyskinesia
Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families
Homozygous mutation in DNAAF4 causes primary ciliary dyskinesia in a Chinese family
Islet primary cilia motility controls insulin secretion.
Identification of Two Novel DNAAF2 Variants in Two Consanguineous Families with Primary Ciliary Dyskinesia
Derivation of Airway Basal Stem Cells from Human Pluripotent Stem Cells
Novel compound heterozygous DNAAF2 mutations cause primary ciliary dyskinesia in a Han Chinese family
A quantitative super-resolution imaging toolbox for diagnosis of motile ciliopathies
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects
Tang X, Ma J, Wang X, Long S, Wan L, Yu H, Yang J, Huang G, Lin T
Journal of Assisted Reproduction and Genetics 2023;40(9):2175-2184
Journal of Assisted Reproduction and Genetics 2023;40(9):2175-2184
A novel mutation in PCD‐associated gene DNAAF3 causes male infertility due to asthenozoospermia
Wan F, Yu L, Qu X, Xia Y, Feng K, Zhang L, Zhang N, Zhao G, Zhang C, Guo H
Journal of Cellular and Molecular Medicine 2023;27(20):3107-3116
Journal of Cellular and Molecular Medicine 2023;27(20):3107-3116
Identification of a novel splice site mutation in the DNAAF4 gene of a Chinese patient with primary ciliary dyskinesia
Xu Y, Wang J, Liu J, Gao Q, Wang B, Xu Z
Asian Journal of Andrology 2023;25(6):713-718
Asian Journal of Andrology 2023;25(6):713-718
Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families
Guo T, Lu C, Yang D, Lei C, Liu Y, Xu Y, Yang B, Wang R, Luo H
Frontiers in Genetics 2022;13
Frontiers in Genetics 2022;13
Homozygous mutation in DNAAF4 causes primary ciliary dyskinesia in a Chinese family
Jiang G, Zou L, Long L, He Y, Lv X, Han Y, Yao T, Zhang Y, Jiang M, Peng Z, Tao L, Xie W, Meng J
Frontiers in Genetics 2022;13
Frontiers in Genetics 2022;13
Islet primary cilia motility controls insulin secretion.
Cho JH, Li ZA, Zhu L, Muegge BD, Roseman HF, Lee EY, Utterback T, Woodhams LG, Bayly PV, Hughes JW
Science advances 2022 Sep 23;8(38):eabq8486
Science advances 2022 Sep 23;8(38):eabq8486
Identification of Two Novel DNAAF2 Variants in Two Consanguineous Families with Primary Ciliary Dyskinesia
Lu C, Yang D, Lei C, Wang R, Guo T, Luo H
Pharmacogenomics and Personalized Medicine 2021;Volume 14
Pharmacogenomics and Personalized Medicine 2021;Volume 14
Derivation of Airway Basal Stem Cells from Human Pluripotent Stem Cells
Hawkins F, Suzuki S, Beermann M, Barillà C, Wang R, Villacorta-Martin C, Berical A, Jean J, Le Suer J, Matte T, Simone-Roach C, Tang Y, Schlaeger T, Crane A, Matthias N, Huang S, Randell S, Wu J, Spence J, Carraro G, Stripp B, Rab A, Sorsher E, Horani A, Brody S, Davis B, Kotton D
Cell Stem Cell 2021;28(1):79-95.e8
Cell Stem Cell 2021;28(1):79-95.e8
Novel compound heterozygous DNAAF2 mutations cause primary ciliary dyskinesia in a Han Chinese family
Sun M, Zhang Y, JiyunYang , Wang Y, Tan H, Wang H, Lei T, Li X, Zhang X, Xiong W, Dou K, Ma Y
Journal of Assisted Reproduction and Genetics 2020;37(9):2159-2170
Journal of Assisted Reproduction and Genetics 2020;37(9):2159-2170
A quantitative super-resolution imaging toolbox for diagnosis of motile ciliopathies
Liu Z, Nguyen Q, Guan Q, Albulescu A, Erdman L, Mahdaviyeh Y, Kang J, Ouyang H, Hegele R, Moraes T, Goldenberg A, Dell S, Mennella V
Science Translational Medicine 2020;12(535)
Science Translational Medicine 2020;12(535)
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
Dong F, Amiri-Yekta A, Martinez G, Saut A, Tek J, Stouvenel L, Lorès P, Karaouzène T, Thierry-Mieg N, Satre V, Brouillet S, Daneshipour A, Hosseini S, Bonhivers M, Gourabi H, Dulioust E, Arnoult C, Touré A, Ray P, Zhao H, Coutton C
The American Journal of Human Genetics 2018;102(4):636-648
The American Journal of Human Genetics 2018;102(4):636-648
Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects
Onoufriadis A, Shoemark A, Schmidts M, Patel M, Jimenez G, Liu H, Thomas B, Dixon M, Hirst R, Rutman A, Burgoyne T, Williams C, Scully J, Bolard F, Lafitte J, Beales P, Hogg C, Yang P, Chung E, Emes R, O'Callaghan C, Bouvagnet P, Mitchison H
Human Molecular Genetics 2014;23(13):3362-3374
Human Molecular Genetics 2014;23(13):3362-3374
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