Kinesin Family Member 5A (KIF5A) antibody

Details for Product No. ABIN184773
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Antigen
Synonyms KIF5A, kif5a, si:ch211-166e11.4, wu:fj61a10, nkhc, my050, spg10, d12s1889, MGC122802, D12S1889, MY050, NKHC, SPG10, D10Bwg0738e, Khc, Kif5, Kns, mKIAA4086
Reactivity
Human, Mouse (Murine)
(39), (25), (23), (1), (1)
Host
Goat
(39), (4)
Clonality
Polyclonal
Application
ELISA
(39), (29), (25), (7), (6), (5), (3), (1)
Pubmed 1 reference available
Quantity 100 µg
Options
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Catalog No. ABIN184773
261.61 $
Plus shipping costs $45.00

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Immunogen C-QAKLFPLHQETAAS
Specificity Human, Mouse
Purification Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Alternative Name KIF5A
Background All names and symbols: KIF5A, kinesin family member 5A, NKHC, N-KHC, D12S1889. Official Symbol: KIF5A. RefSeq number(s): NP_004975. Gene ontology terms: motor, kinesin, membrane fraction, synaptic transmission, adenosinetriphosphatase, microtubule-based movement, non-selective vesicle transport
Gene ID 3798
Research Area Cytoskeleton
Application Notes Peptide ELISA: antibody detection limit dilution 1:16,000. Western Blot: Preliminary experiments gave bands at approx 140, 50, 35 and 20kDa in Human Brain lysates at 1ug of primary. Please note that currently we cannot find an explanation in the literature for the multiple bands we observe given the predicted size of approx. 119Kda according to NP_004975. We would appreciate any feedback from people in the field - have any results been reported with other antibodies/lysates? Have any splice variants/modified forms been reported?
Restrictions For Research Use only
Format Liquid
Buffer 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.
Preservative Sodium azide
Precaution of Use This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage -20 °C
General Reid, Kloos, Ashley-Koch et al.: "A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)." in: American journal of human genetics, Vol. 71, Issue 5, pp. 1189-94, 2002 (PubMed).

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