HAX1 anticorps (Middle Region)
Aperçu rapide pour HAX1 anticorps (Middle Region) (ABIN2784796)
Antigène
Voir toutes HAX1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Middle Region
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Fonction
- HAX1 Antibody - middle region
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Séquence
- QPAPDWGSQR PFHRFDDVWP MDPHPRTRED NDLDSQVSQE GLGPVLQPQP
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Homologie
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 92%, Rabbit: 100%, Rat: 92%, Zebrafish: 91%
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Attributs du produit
- This is a rabbit polyclonal antibody against HAX1. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human HAX1
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP52142-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- HAX1 (HCLS1 Associated Protein X-1 (HAX1))
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Autre désignation
- HAX1
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Sujet
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Background Information: 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.
Gene Name: HCLS1 associated protein X-1
Alternative Symbols: SCN3, HS1BP1, HCLSBP1
Protein Name: HCLS1-associated protein X-1
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Poids moléculaire
- 25
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ID gène
- 10456
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NCBI Accession
- NP_001018238
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UniProt
- O00165
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Pathways
- Regulation of Actin Filament Polymerization
Antigène
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