Anti-Zebrafish SHHA Antibody Picoband®

Mfr.No.	AZQ92008
Antibody Validation	Boster validates all antibodies on WB, IHC, ICC, Immunofluorescence, and ELISA with known positive control and negative samples to ensure specificity and high affinity, including thorough antibody incubations.
Clonality	Polyclonal
Description	Boster Bio Anti-Zebrafish SHHA Antibody Picoband® catalog #AZQ92008. Tested in WB, IHC applications. This antibody reacts with Zebrafish. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Weste blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
Host	Rabbit
Immunogen Region	E.coli-derived zebrafish SHHA recombinant protein (Position: Q208-H409)
Molecular Weight	46 kDa
Positive Control	WB: zebrafish head tissue, whole female zebrafish tissue, whole male zebrafish tissue, zebrafish embryo tissue IHC: zebrafish brain tissue, zebrafish cerebellum tissue, zebrafish muscle tissue, zebrafish colon tissue, zebrafish embryo tissue
Reactivity	Zebrafish
Reconstitution	Adding 0.2 ml of distilled water will yield a concentration of 500 ?g/ml.
Note	Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Gene Name	SHHA
Weight	46 kDa

Dilutions	Weste blot, 0.25-0.5 ?g/ml, Zebrafish Immunohistochemistry, 2-5 ?g/ml, Zebrafish
Form	Lyophilized
Storage	At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Applications	IHC, WB
Description	AZQ92008 is guaranteed for IHC, WB Boster Guarantee

IHC analysis of SHHA using anti-SHHA antibody (AZQ92008). SHHA was detected in a paraffin-embedded section of zebrafish muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 ?g/ml rabbit anti-SHHA Antibody (AZQ92008) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. +2 SHHA was detected in a paraffin-embedded section of zebrafish colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 ?g/ml rabbit anti-SHHA Antibody (AZQ92008) ov

IHC analysis of SHHA using anti-SHHA antibody (AZQ92008). SHHA was detected in a paraffin-embedded section of zebrafish brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 ?g/ml rabbit anti-SHHA Antibody (AZQ92008) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.

Western blot analysis of SHHA using anti-SHHA antibody (AZQ92008). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: zebrafish head tissue lysates.Lane 2: whole female zebrafish tissue lysates.Lane 3: whole male zebrafish tissue lysates.Lane 4: zebrafish embryo tissue lysates.After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHHA antigen affinity purified polyclonal antibody (AZQ92008) at 0.5 ?g/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200)

IHC analysis of SHHA using anti-SHHA antibody (AZQ92008). SHHA was detected in a paraffin-embedded section of zebrafish cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 ?g/ml rabbit anti-SHHA Antibody (AZQ92008) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.

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Combination SKU	Supplier No.	Conjugation	Size	Your price
BHA21011403-1	AZQ92008	Unconjugated	100 ug	$470	Add to Cart
BHA21011403-2	AZQ92008-Biotin	Biotin conjugated	100 ug	$670	Add to Cart
BHA21011403-3	AZQ92008-Cy3	Cy3 conjugated	100 ug	$670	Add to Cart
BHA21011403-4	AZQ92008-Dylight488	Dylight488 conjugated	100 ug	$670	Add to Cart
BHA21011403-5	AZQ92008-Dylight550	Dylight550 conjugated	100 ug	$670	Add to Cart
BHA21011403-6	AZQ92008-Dylight594	Dylight594 conjugated	100 ug	$670	Add to Cart
BHA21011403-7	AZQ92008-FITC	FITC conjugated	100 ug	$670	Add to Cart
BHA21011403-8	AZQ92008-HRP	HRP conjugated	100 ug	$670	Add to Cart
BHA21011403-9	AZQ92008-APC	APC conjugated	100 ug	$770	Add to Cart
BHA21011403-10	AZQ92008-PE	PE conjugated	100 ug	$770	Add to Cart
BHA21011403-11	AZQ92008-iFluor647	iFluor647 conjugated	100 ug	$770	Add to Cart
BHA21011403-12	AZQ92008-carrier-free	Carrier Free	100 ug	$470	Add to Cart

Anti-Zebrafish SHHA Antibody PicobandÂ®

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