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antibody from antibodies-online
Targeting: MLPH
exophilin-3, l(1)-3Rk, l1Rk3, ln, Slac-2a
Western blotAntibody data
- Antibody Data
- Antigen structure
- References [5]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
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- Product number
- ABIN953384 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Melanophilin (MLPH) (AA 540-569), (C-Term) antibody
- Antibody type
- Polyclonal
- Description
- Purified through a Protein A column followed by peptide affinity purification
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 540-569, C-Term
- Vial size
- 0.4 mL
- Storage
- Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts.
Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
Rab GTPases and myosin motors in organelle motility.
Missense mutations in the globular tail of myosin-Va in dilute mice partially impair binding of Slac2-a/melanophilin.
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).
Park JW, Cai J, McIntosh I, Jabs EW, Fallin MD, Ingersoll R, Hetmanski JB, Vekemans M, Attie-Bitach T, Lovett M, Scott AF, Beaty TH
Journal of medical genetics 2006 Jul;43(7):598-608
Journal of medical genetics 2006 Jul;43(7):598-608
Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K
Genetic counseling (Geneva, Switzerland) 2004;15(3):293-301
Genetic counseling (Geneva, Switzerland) 2004;15(3):293-301
Rab GTPases and myosin motors in organelle motility.
Seabra MC, Coudrier E
Traffic (Copenhagen, Denmark) 2004 Jun;5(6):393-9
Traffic (Copenhagen, Denmark) 2004 Jun;5(6):393-9
Missense mutations in the globular tail of myosin-Va in dilute mice partially impair binding of Slac2-a/melanophilin.
Fukuda M, Kuroda TS
Journal of cell science 2004 Feb 1;117(Pt 4):583-91
Journal of cell science 2004 Feb 1;117(Pt 4):583-91
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).
Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G
The Journal of clinical investigation 2003 Aug;112(3):450-6
The Journal of clinical investigation 2003 Aug;112(3):450-6
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Supportive validation
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- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC
