HCLS1 Associated Protein X-1 (HAX1) (Middle Region) Peptide
HAX1
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN977865
Aperçu rapide pour HCLS1 Associated Protein X-1 (HAX1) (Middle Region) Peptide (ABIN977865)
Antigène
HAX1
(HCLS1 Associated Protein X-1 (HAX1))
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- Middle Region
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Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-HAX1 antibody (Catalog #: ARP52141_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Purification
- Purified
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HCLS1 Associated Protein X-1 (HAX1) peptide
HAX1 Reactivité: Humain Hôte: Synthetic BP, Imm
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Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- HAX1 (HCLS1 Associated Protein X-1 (HAX1))
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Sujet
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HAX1 is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease.The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: HCLSBP1, HS1BP1, SCN3
Protein Interaction Partner: HCLS1,IL1A,IQGAP2,ABCB1,ABCB11,ABCB4,CTTN,DGKD,EIF3F,HCLS1,IL1A,KIAA0513,PKD2,YWHAQ,DGKD,EIF3F,IL1A
Protein Size: 279 -
Poids moléculaire
- 31 kDa
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ID gène
- 10456
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NCBI Accession
- NM_006118, NP_006109
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UniProt
- O00165
Antigène
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