Antibody data
- Antibody Data
- Antigen structure
- References [5]
- Comments [0]
- Validations
- Immunocytochemistry [1]
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Validation data
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- Product number
- HPA019036 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA019036, RRID:AB_1846286
- Product name
- Anti-XK
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human XK, Gene description: X-linked Kx blood group, Alternative Gene Names: Kx, NA, NAC, X1k, XKR1, Validated applications: WB, Uniprot ID: P51811, 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
- 0.2 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 Erythroid Differentiation Dependent Interaction of VPS13A with XK at the Plasma Membrane of K562 Cells
Interaction between VPS13A and the XK scramblase is important for VPS13A function in humans
Requirement of Xk and Vps13a for the P2X7-mediated phospholipid scrambling and cell lysis in mouse T cells
XK is a partner for VPS13A: a molecular link between Chorea-Acanthocytosis and McLeod Syndrome
Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein
Amos C, Xu P, De Camilli P
Contact 2023;6
Contact 2023;6
Interaction between VPS13A and the XK scramblase is important for VPS13A function in humans
Park J, Hu Y, Hollingsworth N, Miltenberger-Miltenyi G, Neiman A
Journal of Cell Science 2022;135(17)
Journal of Cell Science 2022;135(17)
Requirement of Xk and Vps13a for the P2X7-mediated phospholipid scrambling and cell lysis in mouse T cells
Ryoden Y, Segawa K, Nagata S
Proceedings of the National Academy of Sciences 2022;119(7)
Proceedings of the National Academy of Sciences 2022;119(7)
XK is a partner for VPS13A: a molecular link between Chorea-Acanthocytosis and McLeod Syndrome
Park J, Neiman A, Brennwald P
Molecular Biology of the Cell 2020;31(22):2425-2436
Molecular Biology of the Cell 2020;31(22):2425-2436
Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein
Urata Y, Nakamura M, Sasaki N, Shiokawa N, Nishida Y, Arai K, Hiwatashi H, Yokoyama I, Narumi S, Terayama Y, Murakami T, Ugawa Y, Sakamoto H, Kaneko S, Nakazawa Y, Yamasaki R, Sadashima S, Sakai T, Arai H, Sano A
Neurology Genetics 2019;5(3)
Neurology Genetics 2019;5(3)
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Supportive validation
- Submitted by
- Atlas Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescent staining of human cell line A-431 shows localization to nucleoplasm & mitochondria.
- Sample type
- Human