Antibody data
- Antibody Data
- Antigen structure
- References [19]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
Submit
Validation data
Reference
Comment
Report error
- Product number
- HPA038440 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA038440, RRID:AB_10671742
- Product name
- Anti-SPAG6
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human SPAG6, Gene description: sperm associated antigen 6, Alternative Gene Names: CT141, pf16, Repro-SA-1, Validated applications: IHC, WB, Uniprot ID: O75602, 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
- 0.4 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 Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants
Novel variants in DNAH6 cause male infertility associated with multiple morphological abnormalities of the sperm flagella (MMAF) and ICSI outcomes
Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice
Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans
Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans
Novel HYDIN variants associated with male infertility in two Chinese families
Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans
Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice
SPAG6 silencing induces autophagic cell death in SKM‑1 cells via the AMPK/mTOR/ULK1 signaling pathway
A quantitative super-resolution imaging toolbox for diagnosis of motile ciliopathies
Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
SPAG6 and L1TD1 are transcriptionally regulated by DNA methylation in non-small cell lung cancers
Profiling cancer testis antigens in non-small-cell lung cancer.
Geng H, Wang K, Liang D, Ni X, Yu H, Tang D, Lv M, Wu H, Li K, Shen Q, Gao Y, Xu C, Zhou P, Wei Z, Cao Y, Sha Y, Yang X, He X
iScience 2024;27(7):110366
iScience 2024;27(7):110366
Novel variants in DNAH6 cause male infertility associated with multiple morphological abnormalities of the sperm flagella (MMAF) and ICSI outcomes
Shao Z, Zhu Y, Gu M, Guo S, Yu H, Li K, Tang D, Xu Y, Lv M
Asian Journal of Andrology 2024;26(1):91-98
Asian Journal of Andrology 2024;26(1):91-98
Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice
Meng G, Wang Y, Luo C, Tan Y, Li Y, Tan C, Tu C, Zhang Q, Hu L, Zhang H, Meng L, Liu C, Deng L, Lu G, Lin G, Du J, Tan Y, Sha Y, Wang L, He W
Human Reproduction Open 2024;2024(1)
Human Reproduction Open 2024;2024(1)
Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility
Guo S, Tang D, Chen Y, Yu H, Gu M, Geng H, Fang J, Wu B, Ruan L, Li K, Xu C, Gao Y, Tan Q, Duan Z, Wu H, Hua R, Guo R, Wei Z, Zhou P, Xu Y, Cao Y, He X, Sha Y, Lv M
Human Genomics 2024;18(1)
Human Genomics 2024;18(1)
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans
Cavarocchi E, Sayou C, Lorès P, Cazin C, Stouvenel L, El Khouri E, Coutton C, Kherraf Z, Patrat C, Govin J, Thierry-Mieg N, Whitfield M, Ray P, Dulioust E, Touré A
iScience 2023;26(8):107354
iScience 2023;26(8):107354
Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans
Lv M, Tang D, Yu H, Geng H, Zhou Y, Shao Z, Li K, Gao Y, Guo S, Xu C, Tan Q, Liu C, Guo R, Wu H, Duan Z, Zhang J, Wang G, Hua R, Fu F, Wang K, Xu Y, Zhou P, Wei Z, Zhang F, Cao Y, He X
International Journal of Biological Sciences 2023;19(2):393-411
International Journal of Biological Sciences 2023;19(2):393-411
Novel HYDIN variants associated with male infertility in two Chinese families
Yu H, Shi X, Shao Z, Geng H, Guo S, Li K, Gu M, Xu C, Gao Y, Tan Q, Duan Z, Wu H, Hua R, Guo R, Wei Z, Zhou P, Cao Y, He X, Li L, Zhang X, Lv M
Frontiers in Endocrinology 2023;14
Frontiers in Endocrinology 2023;14
Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans
Li D, Yang X, Tu C, Wang W, Meng L, Lu G, Tan Y, Zhang Q, Du J
Asian Journal of Andrology 2022;24(4):359-366
Asian Journal of Andrology 2022;24(4):359-366
Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF
Xu C, Tang D, Shao Z, Geng H, Gao Y, Li K, Tan Q, Wang G, Wang C, Wu H, Li G, Lv M, He X, Cao Y
Reproductive Biology and Endocrinology 2022;20(1)
Reproductive Biology and Endocrinology 2022;20(1)
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan L, Cao Y, Lin G, Tan Y
The American Journal of Human Genetics 2022;109(1):157-171
The American Journal of Human Genetics 2022;109(1):157-171
Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
Li K, Wang G, Lv M, Wang J, Gao Y, Tang F, Xu C, Yang W, Yu H, Shao Z, Geng H, Tan Q, Shen Q, Tang D, Ni X, Wang T, Song B, Wu H, Huo R, Zhang Z, Xu Y, Zhou P, Tao F, Wei Z, He X, Cao Y
Journal of Assisted Reproduction and Genetics 2021;39(1):251-259
Journal of Assisted Reproduction and Genetics 2021;39(1):251-259
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice
Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, Tan C, Nie H, Li D, Zhang H, Gong F, Hu L, Lu G, Xu W, Lin G, Zhang F, Cao Y, Tan Y
The American Journal of Human Genetics 2021;108(8):1466-1477
The American Journal of Human Genetics 2021;108(8):1466-1477
SPAG6 silencing induces autophagic cell death in SKM‑1 cells via the AMPK/mTOR/ULK1 signaling pathway
Zhang M, Luo J, Luo X, Liu L
Oncology Letters 2020;20(1):551-560
Oncology Letters 2020;20(1):551-560
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)
Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice
He X, Liu C, Yang X, Lv M, Ni X, Li Q, Cheng H, Liu W, Tian S, Wu H, Gao Y, Yang C, Tan Q, Cong J, Tang D, Zhang J, Song B, Zhong Y, Li H, Zhi W, Mao X, Fu F, Ge L, Shen Q, Zhang M, Saiyin H, Jin L, Xu Y, Zhou P, Wei Z, Zhang F, Cao Y
The American Journal of Human Genetics 2020;107(3):514-526
The American Journal of Human Genetics 2020;107(3):514-526
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella
Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan Y
Scientific Reports 2019;9(1)
Scientific Reports 2019;9(1)
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
SPAG6 and L1TD1 are transcriptionally regulated by DNA methylation in non-small cell lung cancers
Altenberger C, Heller G, Ziegler B, Tomasich E, Marhold M, Topakian T, Müllauer L, Heffeter P, Lang G, End-Pfützenreuter A, Döme B, Arns B, Klepetko W, Zielinski C, Zöchbauer-Müller S
Molecular Cancer 2017;16(1)
Molecular Cancer 2017;16(1)
Profiling cancer testis antigens in non-small-cell lung cancer.
Djureinovic D, Hallström BM, Horie M, Mattsson JSM, La Fleur L, Fagerberg L, Brunnström H, Lindskog C, Madjar K, Rahnenführer J, Ekman S, Ståhle E, Koyi H, Brandén E, Edlund K, Hengstler JG, Lambe M, Saito A, Botling J, Pontén F, Uhlén M, Micke P
JCI insight 2016 Jul 7;1(10):e86837
JCI insight 2016 Jul 7;1(10):e86837
No comments: Submit comment
Enhanced validation
- Submitted by
- Atlas Antibodies (provider)
- Enhanced method
- Recombinant expression validation
- Main image
- Experimental details
- Western blot analysis in control (vector only transfected HEK293T lysate) and SPAG6 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (~3.1 kDa) in mammalian HEK293T cells, LY406761).
- Sample type
- Human
- Protocol
- Protocol
Supportive validation
- Submitted by
- Atlas Antibodies (provider)
- Enhanced method
- Orthogonal validation
- Main image
- Experimental details
- Immunohistochemistry analysis in human fallopian tube and colon tissues using Anti-SPAG6 antibody. Corresponding SPAG6 RNA-seq data are presented for the same tissues.
- Sample type
- Human
- Protocol
- Protocol