FASN - Antibodies - The Human Protein Atlas


	Antibody HPA006461	Antibody HPA056108	Antibody CAB005192	Antibody CAB015417

ANTIBODY INFORMATION
Provider	Atlas Antibodies Sigma-Aldrich	Atlas Antibodies Sigma-Aldrich	Santa Cruz Biotechnology	Santa Cruz Biotechnology
Product name	HPA006461	HPA056108	sc-20140	sc-55580
Host species	Rabbit	Rabbit	Rabbit	Mouse
Clonalityⁱ The antibodies are designated mAB for monoclonal and pAb for polyclonal.	pAb	pAb	pAb	mAb
Purity	Affinity purified using the PrEST-antigen as affinity ligand	Affinity purified using the PrEST-antigen as affinity ligand	Protein A/G	Protein A/G
Released in versionⁱ The release of the Human Protein Atlas in which the antibody was first published.	4.1	14	3.1	4.1
Referencesⁱ References to publications in which the antibody has been used.	1
Proper citation	Atlas Antibodies Cat#HPA006461, RRID:AB_1848437	Atlas Antibodies Cat#HPA056108, RRID:AB_2683039	Santa Cruz Biotechnology Cat#sc-20140, RRID:AB_2101095	Santa Cruz Biotechnology Cat#sc-55580, RRID:AB_2231427
Validation summaryⁱ All assays through which the antibody has been validated. Assays&annotation provide a detailed description of the different assays. The pie-charts indicate degree of validation.	ICC IHC WB PA	N/A ICC IHC WB PA	ICC IHC WB N/A PA	N/A ICC IHC N/A WB N/A PA
IMMUNOCYTOCHEMISTRYⁱ Immunocytochemistry is used to validate the antibody staining and for assessing and validating the protein expression pattern in selected human cell lines. Read more
Validationⁱ Results of validation by standard or enhanced validation. Standard validation is based on concordance with available experimental gene/protein characterization data in the UniProtKB/Swiss-Prot database. Standard validation results in scores Supported, Approved or Uncertain. Enhanced validation is performed using either siRNA knockdown, tagged GFP cell lines or independent antibodies. For the siRNA validation the decrease in antibody-based staining intensity upon target protein downregulation is evaluated. For the GFP validation the signal overlap between the antibody staining and the GFP-tagged protein is evaluated. For the independent antibodies validation the evaluation is based on comparison of the staining of two (or more) independent antibodies directed towards independent epitopes on the protein. For all cases except the siRNA validation, an image representative of the antibody staining pattern is shown. For the siRNA validation, a box plot of the results is shown. Read more	Supportedⁱ Immunocytochemistry is used for validating antibody reliability by assessing staining pattern in cell lines. Validation scores include Enhanced, Supported, Approved and Uncertain. Read more Location supported by experimental gene/protein characterization data and >=1 other antibody Immunofluorescent staining of human cell line A-431 shows localization to plasma membrane & cytosol.		Supportedⁱ Immunocytochemistry is used for validating antibody reliability by assessing staining pattern in cell lines. Validation scores include Enhanced, Supported, Approved and Uncertain. Read more Location supported by experimental gene/protein characterization data and >=1 other antibody Immunofluorescent staining of human cell line U-2 OS shows localization to cytosol.

Antibody dilution	Human assay: A-431 fixed with PFA, dilution: 1:20 Human assay: U-2 OS fixed with PFA, dilution: 1:20 Human assay: U-251 MG fixed with PFA, dilution: 1:20		Human assay: A-431 fixed with PFA, dilution: 1:19 Human assay: U-2 OS fixed with PFA, dilution: 1:19 Human assay: U-251 MG fixed with PFA, dilution: 1:19
IMMUNOHISTOCHEMISTRYⁱ Immunohistochemistry is used for validating antibody reliability by assessing staining pattern in 44 normal tissues. Validation scores include Enhanced, Supported, Approved and Uncertain. Read more
Validationⁱ Results of validation by standard or enhanced validation based on assessment of antibody performance in 44 normal tissues. Standard validation results in scores Supported, Approved or Uncertain. An image representative of the antibody staining pattern is shown. Enhanced validation results in the score Enhanced and includes two methods: Orthogonal validation and Independent antibody validation. For orthogonal validation, representative images of high and low expression are shown. For independent antibody validation, four images of each independent antibody are displayed. Read more	Enhanced - Orthogonal Antibody staining mainly consistent with RNA expression data across 36 tissues. HIGH EXPRESSION Breast RNA expression: 57.5 NX LOW EXPRESSION Skeletal muscle RNA expression: 7.5 NX Enhanced - Independent antibodies Protein distribution across 45 tissues similar between the independent antibodies HPA006461 and HPA056108. Breast Colon Lymph node Skeletal muscle	Enhanced - Orthogonal Antibody staining mainly consistent with RNA expression data across 36 tissues. HIGH EXPRESSION Breast RNA expression: 57.5 NX LOW EXPRESSION Skeletal muscle RNA expression: 7.5 NX Enhanced - Independent antibodies Protein distribution across 45 tissues similar between the independent antibodies HPA006461 and HPA056108. Breast Colon Lymph node Skeletal muscle	Enhanced - Orthogonal Antibody staining mainly consistent with RNA expression data across 36 tissues. HIGH EXPRESSION Breast RNA expression: 57.5 NX LOW EXPRESSION Skeletal muscle RNA expression: 7.5 NX	Enhanced - Orthogonal Antibody staining mainly consistent with RNA expression data across 36 tissues. HIGH EXPRESSION Breast RNA expression: 57.5 NX LOW EXPRESSION Skeletal muscle RNA expression: 7.5 NX

Retrievalⁱ Antigen retrieval is a method used to restore/retrieve the epitope (antibody bidning region) of the target protein, cross-linked, and thus masked, during tissue preserving fixative treatment of the tissues. Read more	HIER pH6	HIER pH6	HIER pH6	HIER pH6
Antibody dilution	1:700	1:800	1:800	1:600
Literature conformityⁱ Conformance of the expression pattern with available gene/protein characterization data in scientific literature and data from bioinformatic predictions. UniProt is used as the main source of gene/protein characterization data and when relevant, available publications and other sources of information are researched in depth. Extensive or sufficient gene/protein data requires that there is evidence of existence on a protein level and that a substantial quantity of published experimental data is available from literature and public databases. Limited protein/gene characterization data does not require evidence of existence on a protein level and refers to genes for which only bioinformatic predictions and scarce published experimental data is available.	Partly consistent with extensive gene/protein characterization data.	Partly consistent with extensive gene/protein characterization data.	Partly consistent with extensive gene/protein characterization data.	Partly consistent with extensive gene/protein characterization data.
RNA consistencyⁱ Consistency between immunohistochemistry data and internally generated RNA-seq data is divided into five different categoreies: i) Consistent with RNA expression data, ii) Mainly consistent with RNA expression data, iii) Mainly not consistent with RNA expression data, iv) Not consistent with RNA expression data, and v) No internal RNA expression data available for correlation.	Mainly consistent with RNA expression data.	Mainly consistent with RNA expression data.	Mainly consistent with RNA expression data.	Mainly consistent with RNA expression data.
WESTERN BLOTⁱ A Western blot analysis is performed on a panel of human tissues and cell lines to evaluate antibody specificity. For antibodies with unreliable result a revalidation using an over-expression lysate is performed. Read more
Validationⁱ Western Blot is used for quality control of the polyclonal antibodies generated in the project. After purification, the antibodies are used to detect bands in a setup of lysate and different tissues. The result is then scored Enhanced, Supported, Approved, or Uncertain. Enhanced validation includes five different methods: Genetic validation, Recombinant expression validation, Independent antibody validation, Orthogonal validation and Capture MS validation. Read more	Enhanced - Independent antibodiesⁱ This method is based on comparing the staining pattern using two independent antibodies with no overlapping epitopes. The staining of the two antibodies is compared by Western blot through analyses of samples from at least two cell lysates preferably expressing the target protein at different levels. The results show similar Western Blot patterns achieved with independent antibodies. Antibody band pattern is confirmed by antibody HPA056108. Analysis performed using a standard panel of samples. 229 112 84 48 32 27 17 Antibody dilution: 1:250 Enhanced - Capture MSⁱ This method is based on comparison between the molecular weight of the stained band visualized by the antibody against the protein size obtained by a capture MS method in which multiple gel slices are cut out from the electrophoretic separation of cell lysates of RT4 and U-251 and analysed separately by proteomics. The band detected by the antibody should be equivalent to the same of the intended target protein and its peptide(s). Antibody band pattern is confirmed by capture-MS. 229 112 84 48 32 27 17 Antibody dilution: 1:250	Enhanced - Independent antibodiesⁱ This method is based on comparing the staining pattern using two independent antibodies with no overlapping epitopes. The staining of the two antibodies is compared by Western blot through analyses of samples from at least two cell lysates preferably expressing the target protein at different levels. The results show similar Western Blot patterns achieved with independent antibodies. Antibody band pattern is confirmed by antibody HPA006461. Analysis performed using a standard panel of samples. 250 130 95 72 55 36 28 17 10 Antibody dilution: 1:100 Enhanced - Capture MSⁱ This method is based on comparison between the molecular weight of the stained band visualized by the antibody against the protein size obtained by a capture MS method in which multiple gel slices are cut out from the electrophoretic separation of cell lysates of RT4 and U-251 and analysed separately by proteomics. The band detected by the antibody should be equivalent to the same of the intended target protein and its peptide(s). Antibody band pattern is confirmed by capture-MS. 250 130 95 72 55 36 28 17 10 Antibody dilution: 1:100	Supportedⁱ The staining of an antibody is evaluated by Western Blot through analysis of samples from different cell lysates. A supportive score is given if band(s) of predicted size in kDa (+/-20%) is detected. Band of predicted size in kDa (+/-20%) with additional bands present. Analysis performed using a standard panel of samples. 220 112 84 47 32 26 17 Antibody dilution: 1:500	Uncertainⁱ The staining of an antibody is evaluated by Western Blot through analysis of samples from different cell lysates. A supportive score is given if band(s) of predicted size in kDa (+/-20%) is detected. Target too small/large to be analyzed with the present setup. Analysis performed using a standard panel of samples. Antibody dilution: 1:500
PROTEIN ARRAY
Validationⁱ A protein array containing 384 different antigens including the antibody target is used to analyse antibody specificity. Depending on the array interaction profile the antibody is scored as Supported, Approved, or Uncertain. Read more	Supported Pass with single peak corresponding to interaction only with its own antigen. Antibody specificity analysis with protein arrays. Predicted and matching interactions are shown in green. Antibody dilution: 1:500	Supported Pass with single peak corresponding to interaction only with its own antigen. Antibody specificity analysis with protein arrays. Predicted and matching interactions are shown in green. Antibody dilution: 1:1100
RELEVANT PUBLICATIONS
	Energy intake correlates with the levels of fatty acid synthase and insulin-like growth factor-1 in male and female C57BL/6 mice Ramdhave AS et al Am J Transl Res 2017;9(3):830-844 Application: WB
ANTIGEN INFORMATION
Antigen	Recombinant protein fragment	Recombinant protein fragment	Recombinant protein	Recombinant protein
Length (aa)	112	115
Antigen sequence	`RWLRVTVAGGVHISGLHTESAPRRQQEQQVPILEKFCFTPHTEEGCLSER AALQEELQLCKGLVQALQTKVTQQGLKMVVPGLDGAQIPRDPSQQELPRL LSAACRLQLNGN`	`MPFRGYAVLGGERGGPEVQQVPAGERPLWFICSGMGTQWRGMGLSLMRLD RFRDSILRSDEAVKPFGLKVSQLLLSTDESTFDDIVHSFVSLTAIQIGLI DLLSCMGLRPDGIVG`
Matching transcripts	FASN-201 - ENSP00000304592 [100%] FASN-206 - ENSP00000488964 [100%]	FASN-201 - ENSP00000304592 [100%] FASN-206 - ENSP00000488964 [100%]
Matching mouse transcripts	ENSMUSP00000052872 [64%] ENSMUSP00000145585 [64%] ENSMUSP00000078337 [25%] ENSMUSP00000026710 [22%]	ENSMUSP00000052872 [80%] ENSMUSP00000145585 [80%] ENSMUSP00000069669 [28%] ENSMUSP00000153669 [23%]
ANTIGEN VIEWⁱ The protein browser displays the antigen location on the target protein(s) and the features of the target protein. The tabs at the top of the protein view section can be used to switch between the different splice variants to which an antigen has been mapped. At the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. A yellow triangle on the bar indicates a <100% sequence identity to the protein target. Below the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen (read more). The curve in blue displays the predicted antigenicity i.e. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. (read more). If a signal peptide is predicted by a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius (turquoise) and/or transmembrane regions (orange) are predicted by MDM, these are displayed. Low complexity regions are shown in yellow and InterPro regions in green. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed (read more), and at the bottom of the protein view is the protein scale.
FASN-201 FASN-206