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MLPH / Melanophilin Antibody (aa577‑590) LS‑C55104 Best Seller
Note: This antibody replaces LS-C72415
Melanophilin antibody LS-C55104 is an unconjugated goat polyclonal antibody to Melanophilin (MLPH). Validated for IF, Peptide-ELISA and WB.
Catalog
Size
Price
LS-C55104-100
100 µg (0.5 mg/ml)
Unavailable

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Product Description

Melanophilin antibody LS-C55104 is an unconjugated goat polyclonal antibody to Melanophilin (MLPH). Validated for IF, Peptide-ELISA and WB.
About MLPH / Melanophilin
MLPH / Melanophilin is a member of the exophilin subfamily of Rab effector proteins. The protein forms a ternary complex with the small Ras-related GTPase Rab27A in its GTP-bound form and the motor protein myosin Va. A similar protein complex in mouse functions to tether pigment-producing organelles called melanosomes to the actin cytoskeleton in melanocytes, and is required for visible pigmentation in the hair and skin. Q9BV36 NM_024101 NP_077006.1

MLPH Antibody, Exophilin-3 Antibody, L1Rk3 Antibody, Ln Antibody, L(1)-3Rk Antibody, Slac-2a Antibody, SLAC2-A Antibody, Synaptotagmin-like protein 2a Antibody, Melanophilin Antibody, SLAC2A Antibody


Specifications

Target
Mouse MLPH / Melanophilin
Host
Goat
Clonality
Polyclonal
Conjugations
Unconjugated
Purification
Immunoaffinity purified
Modifications
Unmodified
Applications
  • Immunofluorescence
  • Western blot (0.5 - 2 µg/ml)
  • Peptide Enzyme-Linked Immunosorbent Assay (1:32000)
Immunogen
Synthetic peptide C-ARHIFAKPVMAQQP from the C-terminus of mouse MLPH / Melanophilin (NP_443748.2). Percent identity with other species by BLAST analysis: Mouse (100%), Rat (100%).
Epitope
aa577-590
Specificity
Mouse MLPH / Melanophilin.
Presentation
Tris-buffered saline, pH 7.3, 0.5% BSA, 0.02% sodium azide
Storage
Aliquot and store at -20°C. Avoid freeze-thaw cycles.
Restrictions
For research use only.
Guarantee
This antibody carries the LSBio 100% Guarantee.

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Images


Immunofluorescence

Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.
Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.

Western blot

Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.
Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.

Western blot

Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.
Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.

Immunofluorescence

Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.
Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.

Western blot

Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.
Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.

Western blot

Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.
Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.

Immunofluorescence

Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.
Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.

Western blot

Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.
Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.

Western blot

Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.
Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.

Immunofluorescence

Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.
Wild-type C57bl6 derived melanocytes were stained with (0.5ug/ml) and detected with Alexa568 conjugated donkey anti-sheep second antibodies. Brightfield image shows melanosome distribution. Data kindly provided by A N Hume, Imperial College.

Western blot

Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.
Antibody staining (0.5 ug/ml) of total melanocyte PNS (200 ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may be the stacking-separating gel interface.

Western blot

Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.
Staining (0.5ug/ml) of total melanocyte PNS (200ug per lane) of wild-type and leaden (Mlph null) mice. The upper band may represent the stacking-separating gel interface. Data kindly provided by A N Hume, Imperial College.


Requested From: 
Date Requested: 6/23/2018

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