FGG antibody (AA 50-330)

Catalog No. ABIN6140620

This Rabbit Polyclonal antibody specifically detects FGG in WB. It exhibits reactivity toward Human.

Quick Overview for FGG antibody (AA 50-330) (ABIN6140620)

Target: FGG (Fibrinogen gamma Chain (FGG))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FGG antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-FGG Antibody

Binding Specificity: AA 50-330

Sequence: GIADFLSTYQ TKVDKDLQSL EDILHQVENK TSEVKQLIKA IQLTYNPDES SKPNMIDAAT LKSRKMLEEI MKYEASILTH DSSIRYLQEI YNSNNQKIVN LKEKVAQLEA QCQEPCKDTV QIHDITGKDC QDIANKGAKQ SGLYFIKPLK ANQQFLVYCE IDGSGNGWTV FQKRLDGSVD FKKNWIQYKE GFGHLSPTGT TEFWLGNEKI HLISTQSAIP YALRVELEDW NGRTSTADYA MFKVGPEADK YRLTYAYFAG GDAGDAFDGF DFGDDPSDKF F

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 50-330 of human FGG (NP_000500.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for FGG

Target: FGG (Fibrinogen gamma Chain (FGG))

Alternative Name: FGG

Background: The protein encoded by this gene is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia. Alternative splicing results in transcript variants encoding different isoforms.,FGG,Cardiovascular,Blood,Coagulation,FGG

Molecular Weight: 49 kDa/51 kDa

Gene ID: 2266

UniProt: P02679