Anti-F10 항체 (CAB1452)

Antibody Name:	Anti-F10 Antibody
Antibody SKU:	CAB1452
Antibody Size:	20uL, 50uL, 100uL
Application:	WB IF
Reactivity:	Human, Mouse
Host Species:	Rabbit
Immunogen:	Recombinant fusion protein containing a sequence corresponding to amino acids 235-488 of human F10 (NP_000495.1).

Application:	WB IF
Recommended Dilution:	WB 1:500 - 1:2000 IF 1:10 - 1:100
Reactivity:	Human, Mouse
Positive Samples:	Raji, Mouse liver

Immunogen:	Recombinant fusion protein containing a sequence corresponding to amino acids 235-488 of human F10 (NP_000495.1).
Purification Method:	Affinity purification
Storage Buffer:	Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Isotype:	IgG
Sequence:	IVGG QECK DGEC PWQA LLIN EENE GFCG GTIL SEFY ILTA AHCL YQAK RFKV RVGD RNTE QEEG GEAV HEVE VVIK HNRF TKET YDFD IAVL RLKT PITF RMNV APAC LPER DWAE STLM TQKT GIVS GFGR THEK GRQS TRLK MLEV PYVD RNSC KLSS SFII TQNM FCAG YDTK QEDA CQGD SGGP HVTR FKDT YFVT GIVS WGEG CARK GKYG IYTK VTAF LKWI DRSM KTRG LPKA KSHA PEVI TSSP LK
Gene ID:	2159
Uniprot:	P00742
Cellular Location:	Secreted
Calculated MW:	54kDa
Observed MW:	75kDa

Synonyms:

F10, FX, FXA

Background:

This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds; the light chain contains 2 EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this gene result in factor X deficiency, a hemorrhagic condition of variable severity. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides.

UniProt Protein Function:	F10: Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of factor Va, calcium and phospholipid during blood clotting. Defects in F10 are the cause of factor X deficiency (FA10D). A hemorrhagic disease with variable presentation. Affected individuals can manifest prolonged nasal and mucosal hemorrhage, menorrhagia, hematuria, and occasionally hemarthrosis. Some patients do not have clinical bleeding diathesis. Belongs to the peptidase S1 family.
UniProt Protein Details:	Protein type:Secreted, signal peptide; EC 3.4.21.6; Secreted; Motility/polarity/chemotaxis; Lipid-binding; Protease Chromosomal Location of Human Ortholog: 13q34 Cellular Component: endoplasmic reticulum lumen; extracellular region; Golgi lumen; plasma membrane Molecular Function:phospholipid binding; protein binding; serine-type endopeptidase activity Biological Process: blood coagulation; blood coagulation, extrinsic pathway; blood coagulation, intrinsic pathway; ER to Golgi vesicle-mediated transport; peptidyl-glutamic acid carboxylation; positive regulation of cell migration; positive regulation of protein kinase B signaling cascade; signal peptide processing Disease: Factor X Deficiency
NCBI Summary:	This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds; the light chain contains 2 EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this gene result in factor X deficiency, a hemorrhagic condition of variable severity. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides. [provided by RefSeq, Aug 2015]
UniProt Code:	P00742
NCBI GenInfo Identifier:	119761
NCBI Gene ID:	2159
NCBI Accession:	P00742.2
UniProt Secondary Accession:	P00742,Q14340,
UniProt Related Accession:	P00742
Molecular Weight:	54,732 Da
NCBI Full Name:	Coagulation factor X
NCBI Synonym Full Names:	coagulation factor X
NCBI Official Symbol:	F10
NCBI Official Synonym Symbols:	FX; FXA
NCBI Protein Information:	coagulation factor X
UniProt Protein Name:	Coagulation factor X
UniProt Synonym Protein Names:	Stuart factor; Stuart-Prower factor
Protein Family:	F107 fimbrial protein
UniProt Gene Name:	F10
UniProt Entry Name:	FA10_HUMAN

	Western blot analysis of extracts of various cell lines, using F10 antibody (CAB1452) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.
	Immunofluorescence analysis of A549 cells using F10 antibody (CAB1452). Blue: DAPI for nuclear staining.

Antibodies	ELISA Kits
Anti-F10 Antibody (CAB15057)	Human Factor 10 (Factor X) ELISA Kit
Cleaved-F10 (A41) Antibody (PACO00044)	Human F10 (Coagulation Factor X) CLIA Kit (HUES00477)
Cleaved-F10 (I235) Antibody (PACO02682)	Human F10 (Coagulation Factor X) ELISA Kit (HUES01903)
	Human Coagulation factor X (F10) ELISA Kit

Secondary Antibody

Anti-HRP Goat Anti-Rabbit IgG (H+L) Antibody (CABS014)